We are always interested in new people…

Please feel free to submit your initiative application and/or CV to ContactUS@spmd-safety.com. All applications received will be reviewed and considered. Please see below a general description of the Safety specialist position.

Safety specialist

If a side effect is reported, it is the Safety Specialist’s responsibility to compile the available information, to enter the information into the safety database, and eventually to conduct the timely submission to competent authorities
(e.g. FDA). Furthermore, the Safety Specialist assumes the role of a Safety Writer when compiling aggregate analyses of the available safety data.

Specific tasks of the Safety Specialist /
Safety Writer include:

  • Data entry into the safety database
  • Submission of reportable case reports to competent authorities (e.g. FDA)
  • Generation of line listing
  • Conduction of literature searches
  • Generation of aggregate safety reports (e.g. PADERs, PBRERs)
  • Generation of Standard Operating Procedures (SOPs)

Desired Qualifications and Skills:

Bachelor or Master Degree in Life-Sciences, Nursing or other Healthcare-related Degree, or similar qualification

  • Good understanding of scientific data and the ability to compile a meaningful and concise narrative and report
  • Attention to detail and a high level of accuracy
  • Candidate should have excellent communication skills, a strong focus on teamwork and should enjoy working in an international environment

It is the policy of spmd – safety strategies for health Inc.  to ensure equal employment opportunity without discrimination or harassment on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, age, disability, marital status, citizenship, national origin, genetic information, or any other characteristic protected by law. spmd – safety strategies for health Inc. prohibits any such discrimination or harassment.


Please send application / resume to: contactUS@spmd-safety.com