Associate Scientific Communications Reviewer

Job Purpose

Responsible for supporting the Pfizer Biopharmaceuticals Group EM Center of Excellence, specifically:

- Working collaboratively with Medical and Marketing teams to review promotional, regulatory, training, and continuing medical education material in compliance with relevant SOPs/ regulations/ industry codes/working practices
- Advocating best practices for achieving effective and compliant medical and promotional communications for Pfizer products
- Under supervision from the 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
- 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 throughout the review process as required
- Ensure clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
- Assist in generating and reviewing any additional support content, including proofreading, reviewing, referencing, and verifying plagiarism of the content

Tactical/ Operational
- Maintain the promotional material review process and system knowledge as per Pfizer standards
- Produce analytical reports and project scorecards as required in line with decided KPIs and share these with the line manager
- Monitor milestones, identify potential risks, and assist in their resolution
- Assist in coordinating activities of other team members to ensure the quality and accuracy of their contributions
- Conduct quality control assessments of assigned deliverables as required

3. Project Planning, Execution, and Delivery
- Prioritize tasks to enhance productivity and manage workload
- Under supervision from line manager, communicate with stakeholders regarding project progress and ensure that quality standards are being met, and optimize efficiency
- Deliver assigned documents on or before the deadline, alerting project teams promptly of any anticipated delays, information gaps, or potential shortcomings in quality

Others

Mentorship - assist in mentoring other team members for effective execution of assigned tasks and goals Keep abreast of current literature, emerging science, technological developments, and medical trends to enhance content review and development Values and Behaviors - Consistently adhere to/demonstrate all Pfizer values, with a special focus on integrity, performance, and teamwork. Work in harmony with internal and external stakeholders Personal Development - Enhance self-development through on-the-job training. In consultation with the line manager, identify additional areas of interest towards learning and development, along with training needs and gaps. Performance Management System (PMS) - Ensure full compliance with PMS

Qualification & Experience
- Post-graduate degree in Pharmaceutical Science or graduate in medical science (MBBS/BDS)
- Prior work experience as a member of the promotional and 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 Areas/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 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 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/ Zinc/ PMAW) is required.

Work Location Assignment: Flexible

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

LI-PFE