Pfizer

Senior Medical Reviewer

Posted Yesterday

Be an Early Applicant

Beijing, CHN

In-Office

Senior level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Review promotional, training, regulatory and medical education materials for scientific and regulatory accuracy; ensure compliance with SOPs, regulations and industry codes; coordinate cross-functional reviews, track milestones and KPIs, perform quality control, mentor team members, and support timely delivery of materials.

Summary Generated by Built In

Job Purpose
Responsible for supporting the Pfizer Research & Development group Medical Information and Review, specifically:

Working collaboratively with Medical and Marketing teams to review promotional, training and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/ working practices
Advocating best practices for achieving effective and complaint medical and promotional communications for Pfizer products
Under supervision from line manager, ensuring that the operational deliverables of assigned deliverables are achieved on or ahead of schedule and within standards such that they meet the desired outcomes (i.e. quality standard, value)

Main Responsibilities
Technical

Uses 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
Liaises with all commercial functions in the review for scientific/ medical accuracy prior to and through the MLR review process as required
Ensuring clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
Collaborating with other lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents
Assists in generating and reviewing any additional support content, including proof reading, reviewing, referencing and verifying anti-plagiarism of the content

Tactical/ Operational

Maintains the promotional material review process and system knowledge as per Pfizer standards
Produces analytics reports and project scorecards as required in line with decided KPIs and sharing these with the line manager
Monitors milestones, identifing potential risks and assisting in resolving any issues
Assists in coordinating activities of other team members to ensure the quality and accuracy of their contributions
Conducts quality control assessments of assigned deliverables as required

Project Planning, Execution and Delivery

Prioritizes and multitasks to enhance productivity and manage workload
Under supervision from line manager, communicates with stakeholders regarding project progress to cross functional teams and ensuring that quality standards are being met and to optimize efficiency
Delivers assigned documents on or before deadline, alerting project teams in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality

Others
Mentorship - actively mentors other team members for effective execution of assigned tasks and goals Keeps abreast of current literature, emerging science, technological developments and medical trends for enhancing content review and development Values and Behaviors - Consistently adheres to/demonstrates all Pfizer values, with special focus on integrity, performance and teamwork. Works in harmony with internal and external stakeholders Personal Development - Enhances self-development through on-the-job training. In consultation with line manager, identifies additional areas of interest towards learning and development, along with training needs and gaps. Performance Management System (PMS) - Ensures full compliance to PMS
Qualification & Experience

Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
Prior work experience as a member of Promotional and more medical/ scientific material review team

Special Skills & Knowledge

Technical skills: Knowledge of "pharmaceutical medicine" including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant Therapeutic Area/Products
Writing skills: Excellent writing skills
Analytic skills: Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them. Analytical skills and reasoning, and sound medical judgment/decision making
Language skill: 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 influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy. 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. (Word, PowerPoint, Excel) is preferred. Working knowledge of tools to aid the promotional material review process (GCMA) is required.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical

Skills Required

Post-graduate degree in Pharmaceutical Science or graduate in Medical science (MBBS)
Prior experience as a member of promotional and medical/scientific material review team
Knowledge of pharmaceutical medicine including clinical pharmacology, medical and paramedical sciences, medical statistics, and relevant therapeutic areas/products
Excellent writing skills
Analytical skills, sound medical judgment and decision making
High fluency in written English and strong functional fluency in spoken English
Strong organizational skills and ability to prioritize multiple projects and meet deadlines
Effective influencing and negotiating skills; ability to work with cross-functional global teams
Familiarity with global regulatory guidance (ICH, FDA, EMA) relevant to clinical and safety data
Working knowledge of tools to aid the promotional material review process (GCMA)
Experience with Word, PowerPoint, Excel
Experience searching academic databases

What the Team is Saying

View all jobs at Pfizer

View Pfizer Profile

Report Job

Am I A Good Fit?

beta

Get Personalized Job Insights.

Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

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.