Senior Software Designer – Life Sciences / Austria (permanent)

On behalf of our Client who are a market leader in certain type of medical devices, pioneering in their field, we are looking for Senior Software Designer to create the vision for the future company applications.

Responsibilities:

  • Design of full stack cross-platform software architectures for company product
  • Managing overall architectural vision and strategy for software products
  • Engagement in the entire software development process
  • Cooperation with development teams on designand code reviews

Requirements:

  • Degree in engineering or equivalent
  • Min. 3 years of experience in application development, ideally with .NET technology or c#
  • Experience in cross-platform and back-end development, Xamarin would be a plus
  • Fluency in English, German not required

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, or please let us know if you may know someone suitable for this role.

Senior Software Designer – Life Sciences / Austria (permanent) was last modified: November 15th, 2017 by Admin

Drug Safety / PV Officer – Pharmaceuticals – UK and Ireland (1.0 FTE, long term contract) / home based in West London

We are currently looking for freelance or permanent Drug Safety / PV Officer to join operations of a pharmaceutical company in UK and Ireland. Preferred location is West London or neighbouring counties. The successful candidate will be responsible for preparing and submitting drug safety-related documents, as well as assessment of adverse event reports.

Responsibilities:

  • Monitoring 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 uptodate
  • Performing safety assessments as needed

Requirements:

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

The role is based in West London. In this position you can expect an excellent prospect of professional development and attractive salary package. 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, or please let us know if you may know someone suitable for this role.

Drug Safety / PV Officer – Pharmaceuticals – UK and Ireland (1.0 FTE, long term contract) / home based in West London was last modified: November 15th, 2017 by Admin

(Sr) R&D Technologist – Solid State/Materials Chemistry, International Company / Poland

Dla naszego Klienta – renomowanej międzynarodowej firmy farmaceutycznej – poszukujemy obecnie kandydatów na stanowisko (Sr) R&D Technologist – Solid State/Materials Chemistry w związku z rozwojem operacji firmy w Polsce.

Zakres obowiązków:

  • Przygotowanie i wdrożenie technologii wytwarzania API
  • Stworzenie produktywnej technologii otrzymywania substancji aktywnej
  • Sporządzanie dokumentacji zgodnie z obowiązującymi procedurami w języku angielskim
  • Dbanie o prawidłowe wykorzystanie materiałów i surowców podczas prac badawczych i doświadczalnych

Wymagania:

  • Min. 3 lata doświadczenia w zakresie chemii ciała stałego (SSC) i znajomość następujących technik: X-ray diffraction, DVS, DSC, TGA and microscopy, PSD measurement
  • Znajomość technik krystalizacji, jak również właściwości form polimorficznych i amorficznych
  • Wykształcenie wyższe ze specjalnością: technologia chemiczna lub inżynieria materiałowa/chemiczna
  • Dobra znajomość języka angielskiego w mowie i piśmie

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) R&D Technologist – Solid State/Materials Chemistry, International Company / Poland was last modified: October 12th, 2017 by Admin

Digital Integrated Circuit 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 Digital Integrated Circuit Designer to join their team working in business unit based in Austria.

Responsibilities:

  • Designing digital modules for mixed-signal integrated circuits for company products
  • Programming in VHDL/Verilog with CAD tools
  • Cooperating with internal teams and third parties
  • Managing for the whole life cycle of the product

Requirements:

  • Degree in Electrical/Electronics Engineering or equivalent education
  • At least 3 years of experience in digital CMOS IC design and of CAD tools
  • Analog design knowledge would be a plus
  • Fluency in English, German would be an advantage

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 or please let me know if you may know someone suitable for this role.

Digital Integrated Circuit Designer – Medical Devices / Austria was last modified: October 4th, 2017 by Admin

Analog Integrated Circuit 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 Analog Integrated Circuit Designer to join their team and work in a new exciting project.

Responsibilities:

  • Designing analog modules for mixed-signal integrated circuits for company products
  • Developing, verifying and drafting circuits and mixed A/D systems with CAD tools
  • Cooperating with internal teams and third parties
  • Taking care for the whole life cycle of the product

Requirements:

  • Degree in Electrical/Electronics Engineering or equivalent education
  • At least 3 years of experience in analog CMOS IC design and of CAD tools
  • Digital design knowledge would be a plus
  • Fluency in English, German would be an advantage

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

Analog Integrated Circuit Designer – Innovative Life Science company / Austria (permanent) was last modified: October 4th, 2017 by Admin

Freelance CRA 0.2-0.3 FTE – International CRO / (home based) Poland

Aktualnie poszukujemy Freelance Clinical Research Associate z min. 3-4-letnim doświadczeniem w monitorowaniu dla firmy CRO o ustabilizowanej pozycji na międzynarodowym rynku, otwierającej właśnie biuro w Warszawie. Wymagana dostępność to idealnie 0.2-0.3 FTE, kontrakt jest przewidziany, w przypadku pozytywnej współpracy, na okres kilku lat.

Do obowiązków na tym stanowisku będzie należeć:

  • zapewnienie zgodności prowadzonego badania ze standardami ICH GCP, jak również z wymaganiami polskiego prawa
  • wizytowanie ośrodków oraz prowadzenie stosownej dokumentacji dotyczącej monitorowanych badań
  • współpraca z innymi członkami zespołu i komunikowanie się na bieżąco w kwestii przebiegu badań z kierownictwem

Wymagania:

  • min. 3 lat doświadczenia w badaniach klinicznych (doświadczenie w onkologii byłoby dodatkowym atutem)
  • wykształcenie w obszarze life sciences (medycyna, farmacja, biologia, lub podobne)
  • dobra znajomość języka angielskiego
  • znajomość pakietu MS Office
  • zdolności organizacyjne i komunikacyjne oraz gotowość do pracy w terenie

Zainteresowane osoby zapraszam do przesłania aktualnego CV po angielsku na adres anna@pharmaprofessionals.eu

Freelance CRA 0.2-0.3 FTE – International CRO / (home based) Poland was last modified: September 27th, 2017 by Admin

(Senior) Clinical Research Associate (Sr CRA) – international CRO, home based, Poland

Poszukujemy (S)CRA z min. 2-letnim doświadczeniem dla firmy CRO o ustabilizowanej pozycji na międzynarodowym rynku, otwierającej biuro w Warszawie. Jest to idealna okazja dla osoby pracującej w dużej firmie, aby zdobyć doświadczenie w składaniu wniosków, negocjacji kontraktów, jak również zarządzania ośrodkami poza standardowymi obowiązkami wynikającymi z natury pracy monitora.

Do obowiązków pracownika na tym stanowisku będzie należeć:

  • zapewnienie zgodności prowadzonego badania ze standardami ICH GCP, jak również z wymaganiami polskiego prawa
  • wizytowanie ośrodków oraz prowadzenie stosownej dokumentacji dotyczącej monitorowanych badań
  • współpraca z innymi członkami zespołu i komunikowanie się na bieżąco w kwestii przebiegu badań z kierownictwem

Wymagania:

  • Preferowane 2 do 3 lat doświadczenia w badaniach klinicznych (doświadczenie w gastroenterologii byłoby dodatkowym atutem)
  • wykształcenie w obszarze life sciences (medycyna, farmacja, biologia, lub podobne)
  • dobra znajomość języka angielskiego
  • znajomość pakietu MS Office
  • zdolności organizacyjne i komunikacyjne oraz gotowość do pracy w terenie

W ofercie jest praca w stabilnym zespole w renomowanej firmie, atrakcyjne wynagrodzenie a poza narzędziami pracy również pakiet benefitów. Zainteresowane osoby zapraszam do przesłania aktualnego CV po angielsku na adres anna@pharmaprofessionals.eu

(Senior) Clinical Research Associate (Sr CRA) – international CRO, home based, Poland was last modified: September 27th, 2017 by Admin

Senior Data Business Analyst – Life Sciences / 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 a Sr Data Business Analyst, who will join their IT department. In this position you will act as an interface between Business Data Governance and IT.

Responsibilities:

  • Strategic overview of Data Governance
  • Indicating business needs in Data Governance and translating them into IT requirements
  • Creating data model according to organization needs
  • Ensuring Data Governance standards across the company

Requirements:

  • Experience in Business Analysis and Data Governance
  • Administration of quality control
  • Good interpersonal and IT skills
  • Fluency in English and at least communicative German

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

Senior Data Business Analyst – Life Sciences / Austria was last modified: September 21st, 2017 by Admin

(Sr) Electrical Automation Engineer – International Company / Poland

Dla naszego Klienta – lidera rynku leków generycznych – poszukujemy obecnie kandydatów na stanowisko (Sr) Electrical Automation Engineer, do zarządzania infrastrukturą systemów automatyki przemysłowej.

Zakres obowiązków:

  • Definiowanie prawidłowego użytkowania systemów automatyki przemysłowej
  • Zarządzanie utrzymaniem ruchu, przeglądy zapobiegawcze, diagnozowanie i przygotowanie planu naprawczego
  • Budowanie procedur i harmonogramów prac utrzymaniowych, modernizacyjnych i optymalizacyjnych dla systemów automatyki przemysłowej klasy DCS, BMS/RMS, PLC, SCADA
  • Sporządzanie dokumentacji technicznej

Wymagania:

  • Min. 2 lata doświadczenia w zakresie systemów automatyki przemysłowej
  • Wykształcenie wyższe ze specjalnością: elektryka, automatyka lub robotyka
  • Dobra znajomość systemów DCS, BMS/RMS, PLC, SCADA, uprawnienia SEP dozorowe i eksploatacji do 1 kV
  • 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

(Sr) Electrical Automation Engineer – International Company / Poland was last modified: August 30th, 2017 by Admin

(Sr) Medical Director in Infectious Diseases / Pediatrics -Top Global CRO / Germany or UK or home based (for an ideal candidate)

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 Infectious Diseases in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in infectious diseases
  • 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 board certification in infectious diseases and experience with pediatrics
  • Experience in clinical development, preferably from CRO or pharma/biotech company
  • Leadership and project management skills
  • Fluency in English, very good interpersonal and communication skills

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 in Infectious Diseases / Pediatrics -Top Global CRO / Germany or UK or home based (for an ideal candidate) was last modified: August 1st, 2017 by Admin

Drug Safety / PV Officer – Pharmaceuticals / Finland (c. 0.5 FTE, home or office based – attractive hourly rate)

We are currently looking for freelance or permanent Drug Safety / PV Officer to join operations of a pharmaceutical company in Finland. Preferred location is Helsinki, although we can consider candidates from other parts of region. The successful candidate 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/regional 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 Finnish and with some command of Swedish

The role is based in Finland. In this position you can expect an excellent prospect of professional development and attractive salary package. 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.

Drug Safety / PV Officer – Pharmaceuticals / Finland (c. 0.5 FTE, home or office based – attractive hourly rate) was last modified: July 13th, 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: August 24th, 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: August 24th, 2017 by Admin

(Sr) Medical Director / Physician, 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 oncology in phases II-III of clinical trials.

In this position you will:

  • Provide internal and external partners with expertise in 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 a medical monitor and medical reviewer for data related to projects
  • Train project teams (both internal and external)

Requirements:

  • Medical Doctor with board certification in oncology and proven clinical experience in oncology and hematology
  • Experience in clinical development 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, Oncology – Top Global CRO / Germany or UK was last modified: July 5th, 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: August 24th, 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

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: August 24th, 2017 by Admin

(Sr) Medical Director (Gastroenterology / Internal Medicine) / 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 with board certification or PhD in Gastroenterology/Gastrointestinal or Internal Medicine
  • Experience in clinical trials, preferably from CRO/pharma/biotech company or 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 / Internal Medicine) / United Kingdom or Germany was last modified: July 31st, 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: August 24th, 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: August 28th, 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: August 24th, 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: August 24th, 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: August 28th, 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) 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: August 24th, 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: August 24th, 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: August 24th, 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: August 24th, 2017 by Admin