Pfizer Senior
Scientific Reviewer Post-graduate degree in Pharmaceutical Science or graduate
in Medical science (MBBS)
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
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
Collates team reports for each region to share with the
medical team
Monitors miletones, 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
Faciliate creation of a robust feedback mechanism to ensure
periodic inputs from stakeholders
Actively participate in 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 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
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.
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