This role requires candidate with previous pharmaceutical operational experience, project management experience, demonstrated agility, and communication skills.

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.