Senior Scientific Reviewer

  Paramedical Vacancy

Job title: Senior Scientific Reviewer

Company: Pfizer

Job description: 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

  • 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 proofreading, 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
  • Collates team reports for each region to share with the medical team
  • Monitors milestones, identifying 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
  • 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 line manager, conduct training and onboarding of newly hired colleagues

3. 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 ensures that quality standards are being met and optimizes efficiency
  • Delivers assigned documents on or before the 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 the line manager, identifies additional areas of interest towards learning and development, along with training needs and gaps. Performance Management System (PMS) – Ensures full compliance with 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 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

Expected salary:

Location: Mumbai, Maharashtra

Job date: Thu, 01 Sep 2022 06:59:23 GMT

Apply for the job now!