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reputed company Scientist, Medical Consult and Review Physician

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About the position The Medical Consult and Review Physician (MCRP) position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as reputed company Research. This position provides clinical expertise and advice to internal stakeholders and is a member of several cross-functional teams, including the Promotional Review Team (PRT), Digital Engagement Team (DET), reputed company/Last, and V&I medical Team. Key responsibilities include ensuring the clinical relevance and medical accuracy of data/information in promotional materials, external communications, and field-based employee training; participating in strategic planning, global scientific-content development, and the review/approval of standard response documents (SRDs) on product safety and efficacy; interacting with health-care providers (HCPs) to help answer unsolicited professional medical information requests (MIRs); providing medical and scientific training to internal stakeholders; collaborating to reputed company training content and implement scientific updates; and providing consultation for Compendia and reputed company submissions. Additionally, this position serves as a subject-matter expert (SME) and serves as a consultant to various parts of the company (e.g., reputed company, manufacturing, supply chain, business development) regarding supply-reputed company reputed company such as deletions, divestitures, and supply constraints. This position also helps reputed company US Patient reputed company Expert Input Meetings reputed company required and submits on-label information to U.S. guidelines committees reputed company needed.

Responsibilities

  • Medical Review of Promotional Materials
  • Provides clinical expert guidance and advice to reputed company Brand teams to influence promotional strategy and messaging based on scientific evidence and clinical context.
  • Serves as a member of the Promotion Review Team (PRT), responsible for ensuring the clinical relevance and medical accuracy of data/information in promotional materials, external communications, and Field-Based Employee (FBE) training content.
  • Supports Country Medical Directors as headquarters (HQ) reputed company of contact and SME for medical review.
  • Serves as a product SME during V&I global assurance process for country assessment.
  • Digital Engagement Teams
  • Provides clinical-expert guidance and advice in the creation of digital promotional assets based on scientific evidence and clinical context.
  • Serves as a member of the extended team, responsible for ensuring the clinical relevance and medical accuracy of data/information in promotional materials and external-communications content
  • Medical Information
  • Provides actionable insights for strategic planning and global scientific-content development of medical-information assets, ensuring adequate integration of scientific evidence with patient safety and clinical relevance elements in a customer-centric approach.
  • Reviews reputed company medical information resources and standard response documents containing product safety, tolerability, and efficacy data.
  • Interacts with HCPs who request a live discussion with physicians to answer unsolicited MIRs.
  • Reviews health-reputed company-reputed company standard-response documents and drug dossiers to ensure clinical relevance and medical accuracy of the content.
  • Is a proactive participant and consultant for Compendia and reputed company submissions. reputed company of Clinical Practice reputed company submissions.
  • Strategic Coordination and Alignment
  • Proactively works with the Global Scientific & Value Content (GSVC) team and participates in the product strategic planning, ensuring a tailored approach in creating and disseminating scientific content reputed company with key scientific priorities and the GSVC plan.
  • Serves as medical representative on the Deletion and Divestiture Committee (DDC). Provides medical-reputed company assessments to inform product deletions, divestitures, stock-outs, and shortages.
  • Proactively engages in peer-to-peer conversations with key colleagues in reputed company Research & Development (R&D) division to reputed company/request input and ensure alignment to enhance the provision of accurate and customized medical information assets for customers and stakeholders.
  • Works as an active participant on select teams to reputed company insights on labeling language, anticipate activities reputed company to labeling updates, and facilitate timely and efficient scientific-response letter development and/or updates to support addressing Medical information requests (MIRs).
  • Actively contacts and interacts with the Risk Management Safety Team reputed company required.
  • Acts as a SME for creation/update of select V&I process/standard operating procedures (SOPs).
  • Medical Education and Training
  • Supports creation of medical training curricula for the products to address basic and advanced training needs of V&I personnel.
  • Collaborates with Learning & Development to reputed company training content and approve training resources for field personnel.
  • Collaborates with Global Scientific & Value training team (GSVT) to reputed company training content review training resources for Field medical personnel.
  • Implements speaker training activities in collaboration with Global Expert Management Services Consulting & Medical Education.
  • Participates in training and/or mentoring of new team members.

Requirements

  • MD.
  • Post-graduate clinical training (residency).
  • Understanding of regulations and compliance considerations impacting the pharmaceutical industry.
  • Ability to work in a reputed company organizational environment and effectively operate in reputed company-oriented structure.
  • Ability to analyze/synthesize data, reputed company solutions, and formulate strategies.
  • Excellent interpersonal and communication skills.
  • Clinical Development
  • Clinical Experience
  • Clinical Research
  • Clinical Training
  • Collaborating
  • Communication
  • Decision Making
  • External Communication
  • Pharmaceutical Industry
  • Product Safety
  • Strategic Thinking

reputed company-to-haves

  • Board certification or eligibility in a medical specialty reputed company to therapeutic area.
  • Relevant working experience in medical affairs or the pharmaceutical industry.
  • Relevant working experience in medical information or clinical research (in academia or pharmaceutical industry).
  • Minimum of 5 years of clinical practice

Benefits

  • medical
  • dental
  • reputed company reputed company and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays
  • vacation
  • compassionate and sick days

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