Senior Scientific Reviewer

Job Description

Responisbilities:

• Use scientific expertise and medical knowledge to ensure appropriate review of promotional, regulatory, training, and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
• Liaise with all commercial functions in the review for scientific/ medical accuracy before and through the review process (on internal Pfizer platforms) as required
• Ensure clear, factual, effective, and concise presentation of analyses and associated discussions in assigned documents
• Collaborate with other lines and relevant project team subject matter experts, to ensure a high standard of accuracy and quality of information presented in assigned documents
• Assist in generating and reviewing any additional support content, including proofreading, reviewing, referencing, and verifying anti-plagiarism aspects of the content

Qualification & Experience:

• Post-graduate degree in pharmaceutical/natural science or graduate in medical (MBBS/BDS/MDS) or allied health sciences
• 2-5 years of prior work experience in promotional content and medical/scientific material review

Special Skills & Knowledge:

• Technical skills: Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant therapeutic areas/products
• Writing skills: Excellent writing skills
• Analytic skills: Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them
• Sound medical judgment/decision making
• Language skills: High fluency in written English and strong functional fluency in spoken English
• Personal skills: Strong organizational skills and ability to prioritize multiple projects and meet deadlines
• Interpersonal skills: Effective persuasive and negotiation skills, including an ability to guide decision-making for document content strategy when appropriate. Ability to work well with all levels and roles in cross-functional, global teams
• Regulatory knowledge:  Familiarity with global regulatory guidance (especially ICH, FDA, and EMA) relevant to clinical and safety data
• Software: Previous experience with software commonly used to present and analyze data and experience with searching academic databases is preferred. Working knowledge of tools to aid the promotional material review process (GCMA/Zinc/PMA)