FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in US Medical Affairs with a focus on oncology, including clinical trial design, evidence generation, and stakeholder engagement. Possesses advanced clinical knowledge and experience in managing cross-functional teams within a complex matrix environment.
Highest-signal resume keywords
Oncology Therapeutic Area KnowledgeClinical Trial DesignEvidence GenerationUS Medical Affairs ExperienceAdvanced Clinical Degree
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchEpidemiologyImplementation ScienceRWE Study DesignIntegrated Evidence PlanningPublication PlanningCompendia SubmissionsAdvisory Board ExperienceScientific Workshop CoordinationMedical Governance
Soft Skills
NetworkingCommunicationInfluencingCross-Functional LeadershipRelationship Building
Certifications & Qualifications
Board Certification in Hematology/OncologyResidency/Fellowship Training in Hematology/OncologyBCOP Certification
Industry Keywords
Multiple MyelomaPlasma Cell DisordersBCMA-Targeted ModalitiesADCsBispecificsCAR-TREMS ProgramNCCNPathwaysField Medical Partnership
About the role
Key responsibilities & impact- Support the US Medical Affairs Lead with development and execution of US medical affairs plans
- Lead planning and execution of medical tactics
- Contribute to medical material development and communication plans
- Apply external stakeholder insights to medical activities
- Partner with Medical Communications & Scientific Training and Medical Information to align materials with US medical strategy and business needs
- Interpret the external environment and competitive knowledge and define the patient journey
- Provide input into selection of US investigator-sponsored studies aligned with the global franchise
- Communicate clinical and market access data requirements for the US market
- Help shape clinical and health outcomes evidence plans for anticipated US market needs
- Contribute to clinical trial design, development plans, and integrated evidence planning
- Coordinate with Global Medical colleagues and R&D technical experts
- Lead or contribute to US scientific engagement with external stakeholders and accounts
- Support appropriate development and use of medicines, disease management, and patient care
- Partner with internal stakeholders to execute medical activities supporting lifecycle management
- Apply sound medical governance to all activities
- Work from home and on-site as needed for team collaboration, stakeholder meetings, and key events
- Travel to meetings and conferences as required
Requirements
What you’ll need- PharmD, PhD, MD or advanced degree
- 4+ years of industry and/or clinical experience in the oncology therapeutic area
- Demonstrated success leading and managing cross-functional work
- Disease and therapeutic area knowledge
- Robust networking, communication, and influencing experience in a complex matrix environment
- Demonstrated ability to build strong internal and external networks
- Advanced clinical or scientific doctorate with hematology/oncology specialization
- Board certification or residency/fellowship training in hematology, oncology, or oncology pharmacy (BCOP)
- Formal training in clinical research, epidemiology, or implementation science
- Direct experience in multiple myeloma or plasma cell disorders
- Familiarity with BCMA-targeted modalities, including ADCs, bispecifics, CAR-T, and sequencing questions
- Experience supporting a product with a REMS program or complex multidisciplinary safety monitoring
- US Medical Affairs experience at a launch or early post-launch asset
- Track record in evidence generation, including RWE study design, ISS/IIS review, integrated evidence planning, and external research collaborations
- Publication and congress planning experience, including authorship on peer-reviewed manuscripts
- Experience with compendia and guideline submissions, including NCCN, pathways, and compendia evidence packages
- Prior work in MLR/promotional review, medical governance, or medical information
- Established relationships with academic and community hematology/oncology key external experts
- Experience with advisory boards, scientific workshops, and peer-to-peer or independent medical education programs
- Field medical partnership experience, including MSL training, insight synthesis, and scientific narrative development
- Experience working across a global/local matrix with Global Medical Affairs and R&D
Benefits
Comp & perks- Annual bonus
- Eligibility to participate in share-based long-term incentive program
- Health care and other insurance benefits for employee and family
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave
- Comprehensive US employee benefits program