job title: Associate pharmacovigilance specialist (clarivate)

Roles and Responsibilities

About You - Education, Experience, Skills

• Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).

• A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage.

• At least 1-2 years of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety)

• Related experience in drug safety/ pharmacovigilance is desirable.

• Strong analytic ability to analyse and summarize the main points of biomedical case reports, studies, or specific topics.

• At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries.

• At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas

• Excellent English language skills (comprehension, speaking, reading, and writing).

• Working knowledge of biomedical terminology, drugs, and therapeutic areas.

• Experience with commercial and client-specific biomedical literature databases.

• Flexibility and adaptability to changing client needs.

• Ability to work effectively, independently, and collaboratively.

• Basic computer literacy.

It would be great if you also had . . .

• Certification from a professional medical writer’s association

• Experience with commercial and client-specific biomedical literature databases

• Scientific/medical writing background