Drug Safety / PV Officer – Pharmaceuticals / Switzerland (0.5 FTE, home or office based – up to 120 CHF per hour)

We are currently looking for freelance or permanent Drug Safety / PV Officer to join operations of a pharmaceutical company based in Switzerland. Preferred location is Zurich, although we can consider candidates from other parts of Switzerland. In this role you will be responsible for preparing and submitting drug safety-related documents, as well as assessment of adverse event reports at local level.

Responsibilities:

  • Monitoring of national pharmacovigilance regulations
  • Preparing and submitting Safety Reports and Risk Management Plans
  • Ensuring all safety information in documents used by the company and third parties is up-to-date
  • Performing safety assessments as needed

Requirements:

  • Master’s Degree in Life Sciences
  • Min. 2-3 years of experience in postmarketing pharmacovigilance and drug safety
  • Working knowledge of Individual Case Study Report processing and management
  • Fluency in English and German or French

The role is based in Switzerland. In this position you can expect an excellent prospect of professional development and attractive salary package. If you meet above criteria and would like to discuss it further, please, send your up-to-date CV to anna@pharmaprofessionals.eu

Drug Safety / PV Officer – Pharmaceuticals / Switzerland (0.5 FTE, home or office based – up to 120 CHF per hour) was last modified: June 20th, 2017 by Admin

Video Designer – Medical Devices / Austria

On behalf of our Client who specializes in design, development and manufacturing of various types of medical devices we are looking for an experienced Video Designer to join their Marketing team working in business unit based in Austria.

Responsibilities:

  • Concept design and production of video and motion graphics content
  • Development of 3D renderings and animations
  • Responsible for captioning and voiceovers for video material for international use
  • Management of video projects

Requirements:

  • Experience in film production from concept to postproduction
  • Minimum of 3 years of experience in creation of 3D animation in V-Ray
  • Knowledge of video and graphic design principles and tools
  • Fluency in English, German is not required

If you are interested in working as a part of international team for a market leader, please send your up-to-date CV in English with contact details to anna@pharmaprofessionals.eu

Video Designer – Medical Devices / Austria was last modified: June 19th, 2017 by Admin

Full Stack Web Developer – Innovative Life Science company / Austria (permanent)

On behalf of our Client who are an international an innovative life science company based in Austria we are looking for Full Stack Developer to join their team and work in a new exciting project.

Responsibilities:

  • Analyzing and solving problems across the stack
  • Building interfaces for various systems and high-quality tools
  • Developing efficient codes that will drive complex web applications
  • Collaborating with product designers and software engineers to deliver compelling user-facing products

Requirements:

  • Degree in IT or equivalent work experience
  • Min. 3 years of experience, ideally with object-oriented programming and ASP.NET C#
  • Experience of frontend development and Javascript, REST, jQuery, HTML/CSS, Bootstrap and AngularJS
  • Fluency in English, German not required

This role is open to international candidates with EU work permit. If you would like to find our more, please send your CV with contact details to anna@pharmaprofessionals.eu and I will contact you with more information.

Full Stack Web Developer – Innovative Life Science company / Austria (permanent) was last modified: June 19th, 2017 by Admin

(Senior) Product Manager OTC – Warsaw / Poland

Naszym Klientem jest międzynarodowa firma farmaceutyczna, której leki są dostępne i sprzedawane na całym świecie. W imieniu tej firmy poszukuję obecnie doświadczonego Kierownika Produktu OTC do pracy w biurze w Warszawie.

Do głównych zadań osoby zatrudnionej na tym stanowisku będą należeć:

  • Tworzenie planów i strategii dla powierzonych produktów, które będą miały przełożenie na konkretne strategie sprzedażowe i efektywność sprzedaży
  • Przygotowywanie kampanii marketingowych
  • Współpraca z zewnętrznymi dostawcami usług marketingowych
  • Zarządzanie powierzonymi produktami oraz przypisanym im budżetem
  • Prowadzenie analiz i badań marketingowych

Oczekiwane kompetencje i doświadczenie:

  • min. 3 lata doświadczenia na analogicznym stanowisku w branży farmaceutycznej, preferowane doświadczenie w obszarze OTC, dodatkowym atutem byłoby doświadczenie w obszarze Rx
  • Wykształcenie wyższe
  • Rozumienie rynku farmaceutycznego oraz sprzężenia marketingu ze sprzedażą
  • Dynamiczna osobowość, wysoka kreatywność, zdolność analitycznego myślenia
  • Dobra znajomość języka angielskiego

Stanowisko oferuje atrakcyjne wynagrodzenie oraz możliwość rozwoju zawodowego w dynamicznie rozwijającej się firmie. Osoby spełniające powyższe kryteria i zainteresowane stanowiskiem, zapraszam do przesłania aktualnego CV wraz z danymi kontaktowymi na adres anna@pharmaprofessionals.eu

(Senior) Product Manager OTC – Warsaw / Poland was last modified: May 19th, 2017 by Admin

(Sr) Embedded Software / Firmware Engineer – Global Life Science Company / Austria

On behalf of our Client who specialize in design, development and manufacturing of various types of medical devices we are looking for an experienced (Sr) Embedded Software / Firmware Engineer to join their team working in business unit based in Austria.

Responsibilities:

  • Developing embedded software/firmware with C/C++ for microcontrollers
  • Concept development and requirements definition
  • Creating software tests and continuously enhancing the software testing process
  • Performing documentation of product design in line with internal standards description

Requirements:

  • Degree or equivalent in Electronics or similar discipline
  • min. 3 years of experience in programming embedded devices ideally with C/C++ for microcontrollers
  • Knowledge of wireless communication modules would be an asset
  • Fluency in English, German would be a plus

In return you can expect an attractive remuneration and interesting international work environment. If you meet the above criteria and are interested, please send your up-to-date CV with contact details to anna@pharmaprofessionals.eu

(Sr) Embedded Software / Firmware Engineer – Global Life Science Company / Austria was last modified: May 10th, 2017 by Admin

(Sr) Procurement / Purchasing Specialist – International Pharma / Poland

Dla naszego Klienta – renomowanej międzynarodowej firmy farmaceutycznej – poszukujemy obecnie kandydatów na stanowisko (Sr) Procurement/Purchasing Specialist w związku z rozwojem operacji firmy w Polsce.

Zakres obowiązków:

  • Realizacja projektów dotyczących zakupów i ich optymalizacji oraz zgodności ze strategią zakupową firmy
  • Odpowiedzialność za przestrzeganie przepisów prawa w zakresie powierzonych obowiązków i procedur zakupowych
  • Efektywne prowadzenie negocjowanie z dostawcami
  • Sporządzanie raportów i analiz dotyczących obszaru zakupów
  • Dbanie o jakość dostarczanych urządzeń, produktów i usług

Wymagania:

  • Min. 3 lata doświadczenia na podobnym stanowisku w jednym z obszarów zakupowych: IT, maszyn przemysłu farmaceutycznego/spożywczego/FMCG, materiałów i usług inżynieryjnych
  • Dobra znajomość zasad i technik negocjacji
  • Orientacja na cel i współpracę z klientami wewnętrznymi i zewnętrznymi
  • Biegła znajomość języka angielskiego w mowie i piśmie
  • Dobra znajomość narzędzi informatycznych takich jak Outlook, Word, Excel, Power Point

Stanowisko oferuje atrakcyjne wynagrodzenie oraz możliwość rozwoju zawodowego w dynamicznie rozwijającej się firmie. Osoby spełniające powyższe kryteria i zainteresowane stanowiskiem, zapraszam do przesłania aktualnego CV wraz z danymi kontaktowymi na adres anna@pharmaprofessionals.eu

(Sr) Procurement / Purchasing Specialist – International Pharma / Poland was last modified: May 10th, 2017 by Admin

European Regulatory Affairs Expert – International Pharma (Generics) / Spain [EXCLUSIVE SEARCH]

On behalf of our Client who are an International Pharma Group, we are looking for an experienced Regulatory Affairs Specialist to join their team in Spain. In this role you will report to Head of Regulatory Affairs.

Responsibilities:

  • Preparing EU submissions and submitting regulatory dossiers
  • Setting strategies for European branded generic drug registrations
  • Monitoring, preparing and following-up on renewals for all registered products
  • Maintenance of all files and documentation pertaining to regulatory activities
  • Dealing with queries from regulatory bodies and health agencies

Desired experience:

  • Educational background in life sciences
  • Min. 5 years of experience in regulatory affairs with small molecule drugs (generic or innovative)
  • Preferred experience of working with EMA and good knowledge of regulatory procedures in Europe
  • Fluency in English, Spanish would be an extra asset

In return you can expect an attractive remuneration and interesting international work environment. If you meet the above criteria and are interested, please send your up-to-date CV with contact details to anna@pharmaprofessionals.eu

European Regulatory Affairs Expert – International Pharma (Generics) / Spain [EXCLUSIVE SEARCH] was last modified: May 9th, 2017 by Admin

IT Project Manager – Pioneering Medical Devices / Austria

On behalf of our Client who are a market leader in certain type of medical devices, pioneering in their field, we are looking for an IT Project Manager to join their team in Austria. The successful candidate will be responsible for supporting digitalization of development process.

Responsibilities:

  • Working as an interface between R&D and IT departments
  • Installation, configuration and maintenance of software tools
  • Increasing productivity in IT project
  • Cooperating with other parties responsible for SW instruments

Requirements:

  • Degree in Computer Science or related field
  • 5+ years of IT experience, including strong project lead/manager experience
  • Experience in R&D specialist with medical devices will be an extra asset, although is not required
  • Fluency in English and German required

The role is based in Austria. In this position you can expect an excellent prospect of professional development and attractive salary package. If you meet above criteria and would like to discuss it further, please, send your up-to-date CV to anna@pharmaprofessionals.eu

IT Project Manager – Pioneering Medical Devices / Austria was last modified: April 3rd, 2017 by Admin

(Sr) Medical Director / Physician (Pulmonology / Paediatrics) – Top Global CRO / Germany or UK

Our Client are an international Clinical Research Organization, one of the top companies globally in this area. As a result of their growing business, they are looking for new Medical Director who will focus on clinical development in the area of pulmonology / respiratory diseases  with particular focus on paediatrics in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in pulmonology area
  • Contribute to protocol and other study documents creation
  • Cooperate with Drug Safety to ensure that all relevant plans are in place to properly assess safety
  • Act as medical reviewer for data related to projects
  • Train project teams (both internal and external)

Requirements:

  • Medical Doctor with board certification in pulmonology / respiratory diseases and proven clinical practice, preferably also in paediatrics
  • Experience in clinical trials from CRO or pharma/biotech company or as an investigator
  • Leadership and previous project management skills
  • Fluency in English

This role is open for international candidates willing to relocate either to Germany or the UK who are eligible to work in EU. If you would like to find our more, please send your CV with contact details to anna@pharmaprofessionals.eu and I will contact you with more information.

(Sr) Medical Director / Physician (Pulmonology / Paediatrics) – Top Global CRO / Germany or UK was last modified: March 15th, 2017 by Admin

(Sr) Medical Director (Gastroenterology / Gastrointestinal) / United Kingdom or Germany

Our Client is an international drug development organization, one of the top companies globally in this area. As a result of their growing business, they are looking for Medical Director who will focus on clinical development in the area of Gastroenterology/Gastrointestinal in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in Gastroenterology/Gastrointestinal
  • Be responsible for medical monitoring and contribute to protocol and other study documents creation
  • Cooperate with PV to ensure that all relevant plans are in place to properly assess safety
  • Act as medical reviewer for data related to projects
  • Train project teams (both internal and external)

Requirements:

  • Medical Doctor, ideally with a board certification or PhD in Gastroenterology/Gastrointestinal and proven clinical experience in this area
  • Experience in clinical development, preferably from CRO/pharma/biotech company or experience as an investigator in clinical trials
  • Good leadership and project management skills
  • Fluency in English, very good interpersonal and communication skills

This role is also open to international candidates willing to relocate either to Germany or the UK. If you would like to find our more, please send your CV with contact details to piotrk@pharmaprofessionals.eu and I will contact you with more information.

(Sr) Medical Director (Gastroenterology / Gastrointestinal) / United Kingdom or Germany was last modified: May 10th, 2017 by Admin

Head of Manufacturing Science and Technology (MSAT) (Biologics) – Top Global Pharma / Switzerland

On behalf of our Client who are a top global pharmaceutical company based in Switzerland, we are currently looking for Director of Manufacturing Science and Technology (MSAT) who will have strategic responsibility for large molecule product development.

Responsibilities:

  • Technical leadership in drug product development and tech transfer activities
  • Leadership and participation in various internal and external technical projects and teams related to sterile manufacturing
  • Development of strategies for scale-down/scale-up and characterization of manufacturing processes
  • Leading and implementing innovation, best practices and solutions for the drug product manufacturing in collaboration with production, process/formulation development and quality teams
  • Supporting  trouble shooting as well as responsibility for technical reports and documents

Requirements:

  • Preferred an advanced degree in Life Science or Engineering
  • Min. 10 years of experience in pharmaceutical/biotechnology industry, incl. min. 5 years of experience with sterile drug product formulation/process development or manufacturing
  • Strong technical expertise in sterile manufacturing of biologics
  • Good knowledge of relevant regulatory guidelines and practices
  • Fluency in English, French or German would be an extra assets

If you are interested and would like to find out more, please send your up-to-date CV with your contact details to my e-mail at piotrk@pharmaprofessionals.eu

Head of Manufacturing Science and Technology (MSAT) (Biologics) – Top Global Pharma / Switzerland was last modified: February 17th, 2017 by Admin

Medical Software 2nd Level Support Engineer – Medical Devices / Austria

On behalf of our Client who are a market leader in certain type of medical devices, pioneering in their field, we are looking for Medical Software 2nd Level Support Engineer to join their team in Austria.

Responsibilities:

  • Second level assistance to users of company software products
  • Technical troubleshooting and analysis of methods as agreed in relevant documents
  • Management of processes and procedures and relevant documentation as well as writing user manuals
  • Cooperate with other teams responsible for company products
  • Organising internal trainings on company software

Requirements:

  • Degree in Computer Science or related field
  • Great analytical thinking combined with very good communication skills
  • Good working knowledge of Microsoft Office package
  • Fluency in English and German required

If you are interested in working as a part of international team for a market leader, please send your up-to-date CV in English with contact details to anna@pharmaprofessionals.eu and I will contact you with more information.

Medical Software 2nd Level Support Engineer – Medical Devices / Austria was last modified: February 7th, 2017 by Admin

(Sr) User Interface Designer – Innovative Life Science company / Austria (permanent)

On behalf of our Client who are an international and innovative life science company based in Austria we are looking for (Sr) User Interface Designer to join their team and work in a new exciting project.

Responsibilities:

  • Analysis, Design, Development and Testing of application elements for company products
  • Building interfaces for various systems and tools
  • Development of models and drafts applications in order to advance them
  • Collaboration with other teams responsible for applications design

Requirements:

  • Relevant degree or equivalent and min. 2 years of industry experience with user interface design or graphics and UI design tools
  • Experience in designing high quality software which is easy to use and maintain
  • Knowledge of operating systems used primarily on mobile devices
  • Fluency in English, German not required

This role is open to international candidates with EU work permit. If you would like to find our more, please send your CV with contact details to anna@pharmaprofessionals.eu and I will contact you with more information, or please let me know if you may know someone suitable for this role.

(Sr) User Interface Designer – Innovative Life Science company / Austria (permanent) was last modified: January 31st, 2017 by Admin

(Sr) Software Validation Engineer – Global Life Science Company / Austria

Our Client is a leading manufacturer of innovative devices which benefits thousands of individuals in more than 100 countries worldwide. As a result of their growing business, they are looking for a new (Sr) Software Validation Engineer.

Responsibilities:

  • Software quality project management
  • Creation of software tests and continuously enhancing the software testing process
  • Collaborate with team members and utilize technical problem solving to engineer quality into the product
  • Performing analysis of documentation needed for regulatory submissions of company products software
  • Providing internal training and technical assistance

Requirements:

  • IT degree or equivalent
  • min. 3 years of experience with understanding of software quality and validation including testing
  • Experience with regulations for medical device software
  • Great analytical thinking combined with very good communication skills
  • Fluency in English

In return you can expect an attractive remuneration and interesting international work environment. If you meet the above criteria and are interested, please send your up-to-date CV with contact details to anna@pharmaprofessionals.eu

(Sr) Software Validation Engineer – Global Life Science Company / Austria was last modified: January 26th, 2017 by Admin

Business Development Associate – Biotech Company / Belgium

Our Client is a growing company focused on R&D and working closely with academic research groups in small molecule development. Since they are growing, they are looking for the right person to join the Business Development team in their offices in Belgium.

In this role you will:

  • Gain extensive market knowledge on competitors and market environment
  • Prepare presentations, reports and offer proposals
  • Interact with clients with focus on early stage drug discovery
  • Work with Project Management team to build and foster client relationships

Requirements:

  • Master’s or PhD degree in a life sciences discipline, business degree will be an asset
  • Min. 1-2 years of experience in BD/sales/licensing in a life science environment; experience in or knowledge of drug discovery would be an advantage
  • Demonstrated ability to establish and maintain strong business relationships
  • Fluency in English with Dutch or French as advantages

If you are open to new challenges and would like to discuss this role, please send your up-to-date CV in English with your contact details to piotrk@pharmaprofessionals.eu

Business Development Associate – Biotech Company / Belgium was last modified: January 18th, 2017 by Admin

Head of Clinical Development – Deputy CSO (Gynaecology) – Innovative Global Pharma / Spain or France [EXCLUSIVE SEARCH]

On behalf of our Client who are an international pharmaceutical company, we are looking for Head of Clinical Development who will act as Deputy CSO and will be responsible for creating clinical development plans, as well as supervising teams and projects in RA, PV and other areas. This role may be based either in Madrid or in Paris.

Responsibilities:

  • Acting as Deputy Chief Scientific Officer in development of new drugs and devices in women’s health
  • Leading clinical development strategy and creating clinical development plans as well as overseeing their execution
  • Evaluating and assessing medical and scientific information to decide on clinical development directions
  • Overseeing RA, PV, scientific and project management teams

Requirements:

  • Preference for Medical Doctor (Physician) with expertise in gynaecology
  • 10+ years of experience in creating and leading clinical development plans in a pharma company/CRO in phases I-IV
  • Experience of bringing molecules to regulatory approval
  • Good knowledge of KOLs in gynaecology as well as the current directions in pharma industry
  • Fluency in English, other languages will be an asset

If you would like to find out more, please send your up-to-date CV in English to piotrk@pharmaprofessionals.eu

Head of Clinical Development – Deputy CSO (Gynaecology) – Innovative Global Pharma / Spain or France [EXCLUSIVE SEARCH] was last modified: January 24th, 2017 by Admin

Senior Project Manager Biology (Small Molecule) – Pharma Company / Belgium

Are you interested in a position of Team Leader/Senior Project Manager responsible for small molecule research? Have you possibly worked for a big pharma so far and would like to have more impact on projects? If you would you like to join a small organization that will let you remain focused on research of new small molecule drug products – we want to hear from you.

Our Client is a growing company focused on R&D and working closely with academic research groups in small molecule development. Since they are growing, they are looking for the right person to join the research team in their offices in Belgium.

In this role you will:

  • Lead project teams of a few researchers
  • Work on various aspects of drug discovery, e.g. target validation, identification of biomarkers, etc.
  • Coordinate activities in small molecule projects, especially related to biology aspects

Requirements:

  • PhD in Biology, Pharmacy or a related discipline
  • Min. 5 years of experience in biological aspect of drug discovery from Pharma industry, peferably in CNS, immunology or inflammation
  • You have worked with small molecule drug discovery
  • Fluency in English, additional languages would be an asset

You can expect a salary that will match your experience. Our Client would offer you an opportunity to work in a dynamic, ambitious environment, where you can grow together with the company. If you are open to new challenges and would like to discuss this role, please send your up-to-date CV in English with your contact details to anna@pharmaprofessionals.eu

Senior Project Manager Biology (Small Molecule) – Pharma Company / Belgium was last modified: January 23rd, 2017 by Admin

(Sr) Regulatory Affairs Specialist (Biotechnology) – International Pharma / Madrid, Spain

On behalf of our Client who are an international Pharma Group currently going through a period of unprecedented expansion, I am looking for an experienced Regulatory Affairs Specialist to join their team in Spain developing biosimilars. In this role you will report to Head of Regulatory Affairs.

Responsibilities:

  • Analyzing global submission requirements and submitting regulatory dossiers
  • Preparation of submission files of new products with respect to local regulations
  • Monitoring, preparing and following-up on renewals for all registered products
  • Participation in various internal and external regulatory meetings as required
  • Maintenance of all files and documentation pertaining to regulatory activities
  • Dealing with queries from regulatory bodies and health agencies

Desired experience:

  • Educational background in life sciences
  • Min. 3 years of experience in regulatory affairs with large molecule / biologic drugs
  • Preferred experience of working with modules 3, 4 and 5
  • Experience of working with EMA and good knowledge of regulatory procedures in Europe
  • Fluency in English, Spanish would be an extra asset

In return you can expect an attractive remuneration and interesting international work environment. If you meet the above criteria and are interested, please send your up-to-date CV with contact details to candidates@pharmaprofessionals.eu

(Sr) Regulatory Affairs Specialist (Biotechnology) – International Pharma / Madrid, Spain was last modified: January 23rd, 2017 by Admin

(Sr) Medical Director in Neurology / United Kingdom or Germany

Our Client is an international drug development organization, one of the top companies globally in this area. As a result of their growing business, they are looking for Medical Director who will focus on clinical development in the area of Neurology in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in Neurology/CNS
  • Be responsible for medical monitoring and contribute to protocol and other study documents creation
  • Cooperate with PV to ensure that all relevant plans are in place to properly assess safety
  • Act as medical reviewer for data related to projects
  • Train project teams (both internal and external)

Requirements:

  • Medical Doctor, ideally with a board certification in Neurology and proven clinical experience in this area
  • Experience in clinical development, preferably from CRO/pharma/biotech company or experience as an investigator in clinical trials
  • Good leadership and project management skills
  • Fluency in English, very good interpersonal and communication skills

This role is also open to international candidates willing to relocate either to Germany or the UK. If you would like to find our more, please send your CV with contact details to anna@pharmaprofessionals.eu and we will contact you with more information.

(Sr) Medical Director in Neurology / United Kingdom or Germany was last modified: January 23rd, 2017 by Admin

(Senior) HVAC and Filtration Maintenance Engineer – International Pharma / Poland

On behalf of our Client, an international pharmaceutical company we are looking for an HVAC Systems Maintenance Engineer to join their Infrastructure Department.

Responsibilities:

  • Maintenance of HVAC systems in pharmaceutical GMP environment
  • Ensuring proper operation and functionality of HVAC systems, working with associated departments of Production, Quality, etc.
  • Creating and maintaining technical documentation according to GMP guidelines and assuring compliance with requirements of relevant authorities
  • Working as a part of engineering team

Requirements:

  • Ideal candidate should have min. 3 years of experience as an HVAC/FiltrationEngineer
  • Relevant qualification, e.g. degree or equivalent in mechanical or electrical engineering
  • Experience in pharmaceutical, biotechnology or food & beverage industry preferred
  • Knowledge of Good Manufacturing Practice (GMP) and the construction of clean rooms

For more information, please send your up-to-date CV with contact details to candidates@pharmaprofessionals.eu

(Senior) HVAC and Filtration Maintenance Engineer – International Pharma / Poland was last modified: January 23rd, 2017 by Admin

GCP QA Manager – Global Drug Development Company / Netherlands

On behalf of our Client who is a top global drug development organisation we are looking for a QA GCP Manager. This is a new role created due to growth of business. This is a great opportunity for an experienced QA GCP Auditor to step up to a management role and gain international experience.

Responsibilities:

  • Managing a team of 3-4 auditors
  • Providing expertise on design, implementation and development of GCP systems and processes
  • Taking part in clinical audits according to relevant SOPs
  • Participating, managing and implementing process improvement activities

Requirements:

  • Degree or equivalent in life sciences discipline
  • Min. 3 years of experience in QA audits with min. 5 years of total experience in clinical trials
  • Great knowledge of GCP environment
  • Fluency in English and willingness to learn Dutch

This role is also open to candidates ready to consider working part time from home (minimum 3 days a week in the office). If you would like to find out more, please send your up-to-date CV to anna@pharmaprofessionals.eu

GCP QA Manager – Global Drug Development Company / Netherlands was last modified: January 23rd, 2017 by Admin

Corporate Communications Manager for LatAm – Global Life Science Company / Austria

For our Client who are a respected name in life science industry we are looking for Corporate Communications Manager responsible for LatAm to become part of corporate communications team based in Austria.

Responsibilities:

  • Management of corporate communications for the company in Latin America area
  • Development, supervision and implementation of corporate strategies
  • Contributing to company communications plan
  • Cooperation with internal and external partners

Requirements:

  • Min. 4-5 years of experience in corporate communications in international environment (experience in pharma/devices industry is not required)
  • Interest in life science environment/industry
  • Great interpersonal and project management skills
  • Fluency in Spanish and/or Portuguese as well as English, German is not required

For this role we can only consider candidates eligible to work in EU. If you would like to discuss it further, please send your CV to piotrk@pharmaprofessionals.eu

Corporate Communications Manager for LatAm – Global Life Science Company / Austria was last modified: January 23rd, 2017 by Admin

(Senior) Clinical Data Manager – Global Pharma / Germany

On behalf of our Client who are a global pharma company we are looking for a (Senior) Clinical Data Manager who will be responsible for data management and working as a part of a project team.

Responsibilities:

  • Data collection and management of multiple clients
  • Responsibility for consistent study data documentation as well as for writing data management and data validation plans
  • Leading discussions with sponsor reviewers
  • Converting database extracted data into standard SDTM format and data quality maintenance

Requirements:

  • Degree or equivalent in life sciences discipline or Mathematics or similar discipline
  • Min. 2 years of experience with data management from within a CRO or a Bio-/Pharma company
  • Excellent numerical skills as well as a drive for quality and consistency
  • Fluent English, German will be an asset

If you are interested in discussing this further, please send your up-to-date CV with contact details to anna@pharmaprofessionals.eu

(Senior) Clinical Data Manager – Global Pharma / Germany was last modified: January 23rd, 2017 by Admin

(Senior) SAS Programmer – Global CRO / Southern Germany

I currently have an attractive opportunity for an experienced SAS Programmer to join a global CRO based in their office in Bavaria in Germany. This role is with one of the most established clinical research organisations with a great track record.  In this role you will be responsible for:

  • Study planning and SAS programming and validation
  • Creating and validating datasets, TFL’s, listings, graphs and analysis for presentation and reporting of clinical data
  • Ensuring all relevant work is performed to company SOPs, Policies, and Guidelines
  • Creation of study specifications for analysis datasets and pooled datase

Requirements:

  • Minimum 2 years of experience as a SAS Programmer
  • Relevant educational background (Life Science, IT, Mathematics or similar)
  • Knowledge of CDISC SDTM and ADaM standards as well as ICH-GCP guidelines
  • Fluent command of English, speaking German is not required

This is a full-time, permanent position. This role is open for candidates from outside Germany who are willing to relocate. In return you can expect an attractive remuneration and an opportunity to work in a multinational environment. For more details please apply with your CV and contact details to anna@pharmaprofessionals.eu

(Senior) SAS Programmer – Global CRO / Southern Germany was last modified: January 23rd, 2017 by Admin

Medical Writing Manager – Top 50 Global Pharma / Germany or USA (East Coast)

On behalf of our Client who are a global top 50 Pharma company we are currently looking for a Medical Writing Manager who will mentor an international team of medical writers and ensure quality across the area being based either in Germany or USA.

In this position you will be responsible for:

  • Leading and coaching a team of a few medical writers
  • Coordination of documentation for regulatory submissions (e.g. investigator brochures, protocols, and clinical study reports) in collaboration with other team members and CROs
  • Writing strategic submission documents
  • Providing technical expertise and liaising with other teams and departments on medical writing
  • Overseeing and supervising CRO medical writing members on a regular basis and reviewing documents generated by CROs

Requirements:

  • Min. 7 years of experience in medical writing for a Pharmaceutical/Biotech company or a CRO
  • Experience in other areas e.g. biostatistics or regulatory affairs will be an extra asset
  • Life science education, PhD would be a plus
  • Knowledge of e-publishing
  • Understanding of regulatory requirements across major geographies
  • Excellent skills in both written and spoken English

In this position you can expect an excellent prospect of professional development in an international work environment and an attractive financial package. If you are interested to find out more, please send your up-to-date CV with contact details to anna@pharmaprofessionals.eu

Medical Writing Manager – Top 50 Global Pharma / Germany or USA (East Coast) was last modified: January 23rd, 2017 by Admin

Medicinal Chemistry Project Manager (Small Molecule) – Pharma Company / Belgium

Are you interested in a position of Team Leader/Project Manager responsible for small molecule research? Have you possibly worked for a big pharma so far and would like to have more impact on projects? If you would you like to join a small organization that will let you remain focused on research of new small molecule drug products – we want to hear from you.

Our Client is a growing company focused on R&D and working closely with academic research groups in small molecule development. Since they are growing, they are looking for the right person to join the research team in their offices in Belgium.

In this role you will:

  • Lead project teams of a few researchers
  • Follow-up on various aspects of drug discovery
  • Coordinate activities in small molecule projects, especially in medicinal chemistry
  • Synthesize, purify and analyze small organic molecules

Who you are:

  • You have a PhD in Chemistry or Pharmacy
  • You have experience in medicinal chemistry from Pharma industry (min. 5 years)
  • You have worked with small molecule drug discovery
  • You speak English fluently

You can expect a salary that will match your experience. Our Client would offer you an opportunity to work in a dynamic, ambitious environment, where you can grow together with the company.

If you are open to new challenges and would like to discuss this role, please send your up-to-date CV in English with your contact details to anna@pharmaprofessionals.eu

Medicinal Chemistry Project Manager (Small Molecule) – Pharma Company / Belgium was last modified: January 23rd, 2017 by Admin

(Sr) Medical Director / Physician (Hematology/Oncology) – Top Global CRO / Germany or UK

My Client are an international Clinical Research Organization, one of the top companies globally in this area. As a result of their growing business, they are looking for a new Medical Director who will focus on clinical development in the area of hematology / oncology in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in hematology / oncology area
  • Contribute to protocol and other study documents creation
  • Cooperate with PV to ensure that all relevant plans are in place to properly assess safety
  • Act as medical reviewer for data related to projects
  • Train project teams (both internal and external)

Requirements:

  • Medical Doctor with board certification in hematology or oncology and proven clinical practice in both areas
  • Experience in clinical development, preferably from CRO or pharma/biotech company
  • Leadership and previous project management skills
  • Fluency in English, very good interpersonal and communication skills

This role is also open to international candidates willing to relocate either to Germany or the UK who are eligible to work in EU. If you would like to find our more, please send your CV with contact details to anna@pharmaprofessionals.eu and I will contact you with more information

(Sr) Medical Director / Physician (Hematology/Oncology) – Top Global CRO / Germany or UK was last modified: January 23rd, 2017 by Admin

(Jr) Clinical Research Associates – Top Global CRO / Moscow, St. Pete or Novosibirsk, Russia

My Client is a predominant name within the drug development sector with and outstanding reputation for delivering clinical research on a global scale. Due to acquisition of new projects, they are looking for Clinical Research Associates at different levels – from Jr CRA to Sr CRA to be based either in one of their offices in Russia or to work from home.

Responsibilities:

  • Site monitoring including close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
  • Site and registry management as prescribed in the project plans
  • Organising and making presentations at Investigator Meetings
  • Participation in the development of protocols and CRFs
  • Liaising with CPM to evaluate needs, resources and timelines

Requirements:

  • Minimum 1 year of experience in monitoring clinical trials
  • Excellent site monitoring and site management skills and understanding of SAEs
  • Degree or equivalent  in a life science discipline
  • Fluency in Russian and English

To apply for this role, please send your CV to anna@pharmaprofessionals.eu

(Jr) Clinical Research Associates – Top Global CRO / Moscow, St. Pete or Novosibirsk, Russia was last modified: January 23rd, 2017 by Admin

(Senior) Clinical Research Associate (home or office based) – Top Global CRO / Belgium

On behalf of our Client who are a Top 5 Global CRO we are looking for a Clinical Research Associate to join their expanding team in Belgium. The position is available at Jr CRA, CRA or Sr CRA level.

Duties:

  • Conducting Pre-Study, Study Initiation, Interim monitoring, and Close-Out visits
  • Maintaining study files, writing clinical trial reports and liaising with vendors
  • Reporting and following up serious adverse events
  • Reviewing progress of projects and initiating appropriate actions to achieve objectives
  • Participation in the development of protocols and Case Report Forms
  • Liaising with CPM to evaluate needs, resources and timelines

Profile:

  • Prior on-site monitoring experience
  • Ability to travel up to 50%, as needed to support project requirements
  • Degree or equivalent in a life science discipline
  • Fluency in English and Dutch or French and some notions of the other language
  • Ability to work independently and proactively
  • Strong communication and team work skills

The company offers great growth opportunities, competitive package and excellent working conditions!
To apply for this role, please send your CV to candidates@pharmaprofessionals.eu

(Senior) Clinical Research Associate (home or office based) – Top Global CRO / Belgium was last modified: January 23rd, 2017 by Admin

Senior Clinical Research Associate (Oncology) – home based / Spain

On behalf of our Client who are a top global Clinical Research Organisation with a widely-recognized name and strong position in the market, I am looking for a SCRA with oncology experience to join their team, working home-based in Spain.

Responsibilities:

  • Site monitoring including close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
  • Site and registry management as prescribed in the project plans
  • Organising and making presentations at Investigator Meetings
  • Reporting and following up serious adverse events
  • Participation in the development of protocols and Case Report Forms
  • Liaising with CPM to evaluate needs, resources and timelines

Requirements:

  • Life science education (Medicine, Pharmacy, Biology, Chemistry or equivalent)
  • Min. 2 years of a full-cycle CRA experience incl. experience of monitoring oncology trials
  • Good knowledge of GCP/ICH guidelines, local regulatory requirements and other applicable regulations
  • Fluent Spanish and English
  • Excellent interpersonal and communication skills

This is an opportunity  with a prospect of an excellent career development. To discuss it further, please send your CV with contact details to candidates@pharmaprofessionals.eu

Senior Clinical Research Associate (Oncology) – home based / Spain was last modified: January 23rd, 2017 by Admin

Associate Director Statistical Programming / Germany

For our client one of the top players in Pharmaceutical market we are looking for Associate Director Statistical Programming. Succesful candidate will utilise their proficiency in SAS programming and team management skills to ensure the highest quality of clinical projects.

Responsibilities:

  • Management of a statistical programmers team
  • Ensuring project quality and timelines
  • Providing expertise in set up and development of Data Management tools for study conduct, supporting statisticians and senior programmers
  • Acting as contact person between third parties (CRO) and statistical programmers team
  • Providing statistical programming Wis/SOPs in the department
  • Cooperation with other clinical trials related teams
  • Ensuring innovative statistical programming techniques and coordination of their implementation

Requirements:

  • Educational background in statistic related discipline eg.  Statistics, Computer Science, or Mathematics or equivalent
  • At least 10 years of experience in statistical programming in clinical development department of pharmaceutical or biotechnology company
  • At least 2 years of team management and project management experience
  • Proficiency in SAS programming
  • Fluency in English

In this position you can expect an excellent prospect of professional development and competitive salary package and benefits. If you meet above criteria and would like to implement your knowledge and experience in dynamic international company please send your CV to candidates@pharmaprofessionals.eu

Associate Director Statistical Programming / Germany was last modified: January 23rd, 2017 by Admin