• Medical Manager GMAIST Hospital BU Jobs in Mumbai,India

  • Pfizer Inc.
  • Save Job
  • 6 - 9 Years
  • Posted : above 1 month

Job Description:


Responsible for providing support to the Pfizer Biopharmaceuticals Group (PBG) Hospital Business Unit (HBU), specifically

Researching literature databases, internal and external repositories to support the evaluation of Health Hazard Assessments and the benefit-risk of Pfizer products
Support for major regulatory agency submissions, clinical overviews, health hazard assessments, listings and summarizing the results of the above research to the required standard
Global Medical Product Evaluation support (GMPE) and reviewing therapy area sales training material for accuracy and alignment This may also include supporting the registry work
Performs pre-medical review of promotional material to ensure it is accurate, truthful, not misleading and aligned with Core Claims, Common Technical and/or other regulatory documents
Supervision and review of the GMPE, promotional material and publications work performed by the associates, in order to provide high quality and timely service
Ensuring delivery of all required activities within expected timelines and on budget
Develop abstracts, posters, manuscripts, congress presentations and slide decks for the HBU as per the required needs
Providing support to the Medical Affairs group including but not limited to literature reviews and summaries, preparation of slide decks

The Medical Manager supports and partners with GMPE TA Leads and Global Medical Affairs by

Creating documents pertaining to clinical data, company data, published literature and other data to support the maintenance and defense of our products Some examples of such document include briefing documents to support meetings with regulatory agencies, clinical overviews and clinical efficacy section in support of PBRERs, ACOs, PSURs, ARs, product renewals health hazard assessments, critical review and analysis of the medical literature and responses to clinical and safety questions from regulatory authorities
Providing expertise and strategic guidance on analysis and presentation of clinical and safety data and on benefit-risk assessment in documents
Assessing document requirements, gauging document complexity, and identfying information gaps or other potential issues In collaboration with the relevant GMPE TA Lead, the author proposes or contributes to strategies to resolve any identified issues
Clinical and scientific medical writing, editing, and quality control review (QC) for regulatory documents including clinical study reports, safety narratives, protocols, protocol amendments, investigator brochures and submission documents
Pharmacovigilance and drug safety writing including Periodic Adverse Drug Experience Reports (PADERs), Periodic Safety Update Reports (PSURs), and Development Safety Update Reports (DSURs)
Manuscript writing including researching, organizing, compiling, interpreting and quality checking various types of technical and/or medical information
Medical communication writing including research and authoring of global medical standard response letters
Creating slides, abstracts, training materials, and style guides, as needed for our clients and their diverse audiences
Adapting writing to different types of clients and audiences from the health care professionals and technical people to the consumer audience
Ensure assigned documents are produced in accordance with relevant internal SOPs and external regulatory guidance, alerting project teams in a timely manner of any definite or potential deviations
Ensure clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents
Deliver assigned documents on or before deadline, alerting project teams in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality
Understand relationships and dependencies between documents and analyses produced for regulators, eg, RMP, DSUR, PBRER, and ACO
Collaborate with other lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents



Writing skills Excellent scientific writing skills, including an ability to summarize and interpret complicated data effectively, concisely and persuasively
Analytic skills Utilize tools such as OvidSP and other bibliographic databases such as PubMed, Medline, Embase, and Biosis Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them
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 Ability to mentor more junior colleagues and external vendors
Regulatory knowledge Familiarity with global regulatory guidance (especially ICH, FDA and EMA) relevant to clinical and safety
Software Previous experience with software commonly used to present and analyze data and experience with searching academic databases (Word, PowerPoint, Excel) is preferred
Epidemiology Familiarity with epidemiologic principles and concepts is desirable


Reports directly to the Senior Medical Manager
Works closely with GMPE Therapeutic Area Leads and Global Medical Affairs Leads
Interacts with Regulatory, Safety and Medical Affairs colleagues, Local, Regional and at a Global level

Education Graduate/Post Graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences or equivalent degrees

Experience 3 to 4 years relevant experience for medical graduates, PhDs & masters in life sciences/ more than 6 years relevant experience for science graduates

Minimum 3 years of experience in medical writing within an agency, CRO, Pharma / Biotech Company
Prior experience in using search tools, developing search strings and assessing search results is preferred

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

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 15th Mar 2020

Key Skills:

Company Profile:

Pfizer Incarfix

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