Instagram
youtube
Facebook

Senior Medical Affairs Scientist (Sr. Mas) – Breast Cancer (Temporary Contract/Secondment) 6 Months

2+ years
Not Disclosed
10 Jan. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Medical Affairs Scientist (Sr. MAS) – Breast Cancer (Temporary Contract/Secondment, 6 Months)

Location: Lisbon, Portugal
Job Type: Full-Time (Temporary Contract/Secondment, 6 months)
Job ID: 4924305
Posted: 1 Day Ago


Position Overview

The Senior Medical Affairs Scientist (Sr. MAS) will lead the execution of medical strategies for assigned products in the therapeutic area of breast cancer. This includes planning and managing medical projects, external engagement with healthcare professionals (HCPs), and cross-functional collaboration. The role is critical in ensuring medical excellence, compliance, and alignment with organizational goals.


Key Responsibilities

Medical Plan Development and Execution

  • Create and execute medical plans for assigned products, ensuring alignment with strategic goals.
  • Lead all medical projects related to assigned products, including advisory boards, educational programs, and budget management.
  • Perform medical reviews for Global Medical Grants (GMG) and manage data generation projects, including real-world evidence.

Stakeholder Engagement

  • Act as the key medical expert for HCPs and Medical Societies.
  • Lead medical-to-medical (M2M) communications, addressing therapeutic guidelines, medical challenges, data gaps, and future trends.
  • Organize and conduct clinical sessions, serving as project owner, speaker, or moderator.
  • Develop and maintain a compliant stakeholder plan aligned with GDPR and Pfizer requirements.

Content Development and Communication

  • Create up-to-date M2M content and tailored materials for HCPs and patients for face-to-face and digital interactions.
  • Ensure content is approved through appropriate review and approval systems.
  • Contribute to omnichannel strategies with relevant scientific content.
  • Update medical interaction tools, tracking HCP inquiries and fostering ongoing M2M discussions.

Cross-Functional Collaboration

  • Collaborate with internal teams, including:
    • Global/Chief Medical Affairs Office (CMAO): Participate in working groups and align with global strategies.
    • Commercial Area: Provide medical input and strategic insights for assigned products.
    • Health & Value (H&V): Support studies and reimbursement dossiers.
    • Regulatory and Supply Chain Quality (SCQ): Offer medical input for lifecycle activities requiring medical expertise.
    • Medical Information and Drug Safety Unit: Provide local medical affairs input on special requests.
  • Lead internal medical training for assigned products.

Compliance and Quality

  • Ensure compliance with medical governance in internal projects and external engagements.
  • Work closely with the Medical Quality Governance Manager (MQGM), Compliance, and Legal teams.
  • Contribute to maintaining high standards of medical quality in all activities.

Required Qualifications

Education and Experience

  • Education:
    • University degree in health or life sciences.
  • Experience:
    • Minimum of 2 years in the pharmaceutical industry or relevant healthcare sector.
    • Proven expertise in:
      • Medical plans and budget management.
      • Medical governance and cross-functional collaboration.
      • Medical writing and document review.
      • Communication across stakeholders and channels.
      • Stakeholder engagement and management.

Skills and Competencies

  • Performance-driven with strong collaboration and networking abilities.
  • Organizational and project management skills with a focus on priorities and resilience.
  • High sense of responsibility, accountability, and quality orientation.
  • Strategic, agile, and innovative mindset with a focus on growth.

Language Requirements

  • Fluency in Portuguese and English.

Equal Opportunity and Disability Inclusion

Pfizer is an equal opportunity employer, ensuring compliance with all equal employment opportunity legislation. As a disability-inclusive employer, Pfizer is committed to providing reasonable adjustments to support candidates throughout the recruitment process and their career.

Start your journey with Pfizer today by applying for this impactful role!