Senior Scientific Reviewer At Pfizer. Interested candidates can check the details given below and can apply online.
Job role: Senior Scientific Reviewer
Job ID: 4886785
Location: India – Mumbai, APAC – Any Pfizer Site
Employment type: Full time
About Us
Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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 to achieve effective and compliant medical and promotional content for Pfizer products
- Under supervision from the line manager, ensuring that the operational deliverables assigned are achieved on or ahead of schedule and within the set standards of quality and value
Main Responsibilities for Senior Scientific Reviewer At Pfizer
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 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
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
- Collate team reports for each region to share with the medical team
- Monitor milestones, identify potential risks, and assist in resolving any issues
- Assist in coordinating the activities of other team members to ensure the quality and accuracy of their contributions
- Conduct quality control assessments of assigned deliverables as required
- Facilitate the creation of a robust feedback mechanism to ensure periodic inputs from stakeholders
- Actively participate in the daily management of the review team. Ensure that the day-to-day activities are conducted smoothly
- Under supervision from the line manager, conduct training and onboarding of newly hired colleagues
Project Planning, Execution, and Delivery
- Prioritizes and multitasks to enhance productivity and manage workload
- Under supervision from the line manager, communicate with cross-functional stakeholders regarding project progress and ensure that quality standards are being met; and optimize efficiency
- Deliver assigned documents on or before the deadline, promptly alerting project teams of any anticipated delays, information gaps, or potential shortcomings in quality
Others
- Mentorship – actively mentors other team members for the effective execution of assigned tasks and goals
- Keep abreast of current literature, emerging science, and technology developments, and medical trends to enhance content review and development
- Values and Behaviors – Consistently adhere to/demonstrates 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/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/PMAW) is requiredWork 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
Here are few interview questions with answers to excel n the interview of the job role Senior Scientific Reviewer At Pfizer:
1.How would you ensure compliance with relevant SOPs, regulations, industry codes, and working practices while reviewing promotional materials?
Answer: During the review process, I would meticulously follow the established standard operating procedures (SOPs) and guidelines provided by regulatory bodies. I would cross-reference the material against applicable regulations and industry codes to ensure compliance. Additionally, I would collaborate closely with the commercial team, medical experts, and other stakeholders to verify the scientific and medical accuracy of the content. By maintaining clear communication channels and continuously updating my knowledge of regulatory requirements, I can ensure the promotional materials meet the necessary compliance standards.
2.Can you describe a time when you encountered a complex scientific issue during the review process and how you resolved it?
Answer: In a previous role, I encountered a scientific issue related to the interpretation of clinical trial data for a promotional material review. To address this challenge, I engaged in comprehensive research, analyzing relevant scientific literature, and consulting subject matter experts within the company. By gathering insights and leveraging my analytical skills, I was able to develop a well-informed perspective on the issue. I presented my findings to the team and engaged in constructive discussions to reach a consensus. Through this collaborative approach and evidence-based decision-making, we successfully resolved the complex scientific issue and ensured accurate and compliant content.
3.How do you prioritize and manage multiple projects with varying deadlines?
Answer: To effectively manage multiple projects, I rely on strong organizational skills and prioritization techniques. First, I assess the urgency and importance of each project, considering factors such as deadlines, impact, and stakeholder requirements. I then create a detailed project plan, breaking down tasks, setting milestones, and allocating sufficient time for each project. Regular communication and coordination with stakeholders help me stay updated on project progress and address any potential issues proactively. Additionally, I leverage tools like project management software to track progress, ensure timely delivery, and promptly communicate any anticipated delays to the relevant teams.
4.How do you stay updated on emerging science, technology developments, and medical trends relevant to your role?
Answer: Staying updated on emerging science, technology developments, and medical trends is essential to my role as a Senior Scientific Reviewer. To achieve this, I adopt a proactive approach by regularly reading scientific literature, attending conferences, and participating in relevant webinars and workshops. I also engage in discussions with colleagues and subject matter experts to share insights and gather different perspectives. Additionally, I follow reputable scientific journals and publications, subscribe to relevant newsletters, and join professional networks to stay abreast of the latest advancements in the field. By dedicating time to continuous learning and leveraging various resources, I ensure that my knowledge remains up to date, enhancing the quality and accuracy of my work as a Scientific Reviewer.
Senior Scientific Reviewer At Pfizer
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