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Discover the Role of an Associate Medical Manager at Pfizer’s Medical Review Services

Discover the Role of an Associate Medical Manager at Pfizer – Medical       Graduate Jobs

Pfizer is a leading global pharmaceutical company that is dedicated to discovering innovative solutions to improve people’s health and well-being. With a focus on research and development, Pfizer strives to bring groundbreaking advancements in healthcare to patients around the world.

Job role – Associate Medical Manager, Medical Review Services (MRS)

Position Summary

The Associate Medical Manager, Medical Review Services supports the Global Medical Affairs team and Global Medical Leads by performing medical pre-review (reference check) of promotional, above brand materials, as well as sales training material. This involves active internal and external stakeholder engagement to coordinate and perform pre-review of materials.

Position Responsibilities – Medical Graduate Jobs

Pre-Medical Review:

  • Performs medical pre-review (reference check) of promotional, above brand materials including but not limited to Health Care Professional (HCP) promotional aids, Web/Social, training material, advertisements, consumer promotions, conventions/ meetings etc to ensure:
    • The claims are accurate, truthful, not misleading and aligned with Core Claims, Common Technical and/or other regulatory documents.
    • The references are adequate, and they fully support the relevant claims.
    • The claims are consistent with the specified reference label used.
  • Manages end-to-end pre-medical review for assigned therapy area sales training materials and relevant materials by Patient Health and Impact (PHI).
  • Conducts reviews independently with minimal supervision, in accordance with relevant internal SOPs and external regulatory guidance, alerting project teams in a timely manner of any definite or potential deviations.
  • Ensures the in-scope promotional, above brand and brand curriculum pieces are reviewed utilizing Automated Machine Learning outputs.
  • Ensures the correct Bot commands are executed to enable efficiency in reviews.
  • Supports scientific congresses through review of content and congress reports in GCMA.
  • Supports review of promotional material/training materials for products other than assigned allocation covering other BUs as well as other therapeutic areas in same BU based on bandwidth.
  • 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.
  • Ensures delivery of all required activities are within expected timelines and on budget.

Stakeholder Management:

  • Engages with Medical Leads and Marketing leads to ensure smooth workflow for reference check of promotional and sales training materials.
  • Develops and sustains constructive relationship within customers and stakeholders.
  • Leads the communication with different stakeholders and their departments for a coordinated structure of functions and workflow.

Education And Experience

Education:

Graduate/Post-graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences or equivalent degrees.

Experience: Medical Graduate Jobs

  • 2 to 3 years relevant experience for medical graduates, PhDs & masters in life sciences/ more than 6 years relevant experience for science graduates.
  • Minimum 2 year of experience in medical writing/review within an agency, CRO, Pharma / Biotech Company.
  • Experience in collaborating with Global stakeholders and managing stringent timelines.
  • Prior experience in medical content creation or promotional material review is preferred.
  • Prior experience in conducting medical reviews or QC of regulatory documents is preferred.

Technical Skills Requirements

  • Review/QC skills: Excellent review or QC skills. Experience in promotional material review or content review would be an asset.
  • Analytical skills: Proficiency in analyzing scientific claims and checking the same against the references. Familiarity with statistical/epidemiologic principles and concepts is desirable. Conducts and interpret analyses and interpret routine medical and safety analyses without guidance from team members.
  • 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 International Conference on Harmonization (ICH), Food and Drug Administration (FDA) and European Medical Agencies (EMA) relevant to clinical and safety.
  • Software: Previous experience with software commonly used to present and analyze data (Word, PowerPoint, Excel) is preferred.
  • Synthesize analyses of medical and scientific data into clearly written text without supervision.
  • Understand medical concepts of the disease and the specific approach to treatment.

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