Scientist Risk Evaluation & Reporting

Highly Competitive
  1. Permanent
  2. Analytical Chemistry
  3. Germany
Frankfurt am Main (60327), Hessen
Posting date: 23 May 2019
SC.AB.23529_1558623676

A global healthcare company is recruiting a Scientist - Risk Evaluation & Reporting to join their German office. This organisation researches, develops, manufactures, and markets innovative and original products, with a focus on pharmaceutical products for the treatment of diseases and nutraceutical products for the maintenance of everyday health. Based in Frankfurt, this is an exciting opportunity to work with a leading pharmaceutical firm that pioneers the challenging field of mental health, along with other global public health issues.

The Scientist - Risk Evaluation & Reporting will assist the medical safety staff (Physicians & Scientists) with monitoring the safety profile of assigned company investigation & marketed products, including devices and combination products through the use of clinical, pharmacological, and epidemiological knowledge.

Job Responsibilities:

  • Maintaining accurate and complete knowledge of assigned investigational and marketed products including devices and combination products.
  • Analysing relevant data and the authoring of specific sections of pre- and post-marketing aggregate reports, RMPs, and other key safety documents.
  • Conducting literature searches and summarizing relevant findings.
  • Identifying, clinically interpreting, and evaluating safety signals for assigned investigational and marketed products.
  • Representing global pharmacovigilance via active participation in cross-functional meetings and committees.

Skills and Requirements:

  • A master degree or PhD in health sciences (nursing, pharmacy, public health, epidemiology or other) with at least 2 years of experience in in drug safety/pharmacovigilance, clinical, or related fields in the pharmaceutical industry. Alternatively, a Bachelor's degree with 5+ years of relevant experience.
  • Knowledge of EU PV regulations and GVP, ICH guidelines and US PV regulations.
  • Experience with Risk Management and Signal Detection preferred.
  • Medical writing experience.
  • Excellent command of the English language.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Andreas Bartelt at a.bartelt@proclinical.com or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-AB2

#Scientific

close