The role will be various medical affairs projects assigned by the medical director such as managing medical financials, assist in cross functional communications.
Be accountable for RMP deliverables and assigned RWE projects:
-RMP, candidate will need to consolidate and draft RMP documentation required by the health authorities for assigned Pfizer products. This also includes reviewing and insuring requirements for RMP documents are provided by cross functional teams.
- Health Authorities Committments: Consolidate, Review, RMP commitment from various cross functional sources
- Narrative Writing: Write clear, concise case narratives summarizing adverse events for health authority submissions.
- RWE, the candiate need to co-ordinate efforts of assigned new or ongoing RWE projects and to manage study issues and compliance with standard processes, policies and procedures. Ensuring and track budget spending match study milestones. Liaise with above country functions to insure study milestones adhere to Pfizer policies and are properly documented
- Managing the internal process in Pfizer system of medical projects, including but not limited to clinical research of secondary database analysis study, non-interventional study, low-interventional study, pragmatic trials, advisory board, publication ...etc.
- Scope of work includes operational strategy, vendor communication, project timeline and milestone oversight, budget monitor, project documentation, publication quality control, and project closure to comply with internal and external operational requirement.
- Other medical affairs projects appointed by supervisor.
- Align with project owner on budget planning, allocation & phasing, tracking & monitor, managing project amendment or deviation requirement; align in and above country medical financial operation.
Basic Qualifications
- Advanced degree in the medical sciences or related discipline.
- Basic experience in clinical research, and/or study management across a range of therapeutic areas
Preferred Qualifications
- 2+ years' experience in the pharmaceutical industry
- Experience in managing finance
- Experience in RMP documentation preparation
- Pharmacist or related degree
- Extensive knowledge in study operational processes.
- Good documentation skills
- Good English verbal and written communications skills
- Audit experience
- With a pharmaceutical or CRO background.
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
Skills Required
- Advanced degree in medical sciences or related discipline
- Basic experience in clinical research and/or study management
- 2+ years' experience in the pharmaceutical industry
- Experience in managing finance
- Experience in RMP documentation preparation
- Good documentation skills
Pfizer Compensation & Benefits Highlights
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Parental & Family Support — U.S. materials describe up to 26 weeks of parental leave (including up to 12 paid non‑medical weeks), with phased return‑to‑work plus fertility, adoption, and surrogacy financial support, backup care, lactation support, and caregiver leave. These offerings indicate depth in family‑building benefits and day‑to‑day caregiver resources.
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Healthcare Strength — Core programs commonly include medical, prescription drug, dental, vision, mental‑health/EAP resources, disability insurance, preventive health programs, and free or reduced‑cost vaccinations. Voluntary Benefit Extras and wellness resources broaden coverage and access.
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Retirement Support — Career pages and postings note a 401(k) with company matching plus an additional company retirement savings contribution in some plans. Company materials also reference financial‑planning education and colleague‑directed retirement funds.
Pfizer Insights
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Employees engage in a combination of remote and on-site work.







