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Roche

Medical Science Liaison, IBD Pipeline

Roche

. Provide clinical and health economic information related to IBD disease states and appropriate utilization of approved and pipeline Genentech medicines .

Posted 9/28/2026full-timeUnited StatesMid-LevelSenior💰 $161,280 - $299,520 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical and health economic information related to IBD, with a strong focus on engaging healthcare providers and decision makers. Proficient in clinical trial management, compliance with regulatory guidelines, and developing strategic medical plans.

Highest-signal resume keywords
Advanced Clinical/Science DegreeProficiency in GCPIn-Depth Knowledge of Clinical Development ProgramsExtensive Field Medical ExperienceFamiliarity with Health Economics and Reimbursement

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ManagementHealth Economic Outcomes ResearchProduct and Safety Profile UnderstandingClinical Operations CollaborationMedical Communications Development
Soft Skills
Relationship BuildingCollaborationCustomer Insight Capture
Tools & Technologies
CRM Systems
Industry Keywords
IBD Disease StatesManaged CareLegal and Regulatory CompliancePharmaceutical IndustryTherapeutic Area Knowledge

About the role

Key responsibilities & impact
  • Provide clinical and health economic information related to IBD disease states and appropriate utilization of approved and pipeline Genentech medicines
  • Engage healthcare providers, population health decision makers, and patients within assigned regions
  • Co-create local medical strategy with regional partners and deliver for customers
  • Exchange scientific and medical information with thought leaders, clinical investigators, related staff, and healthcare decision makers
  • Build, cultivate, and leverage relationships with external scientific and medical customers and organizations
  • Develop engagement plans aligned with customer needs and global strategy
  • Participate in continuous learning and upskilling programs
  • Respond to on- and off-label questions in compliance with legal, regulatory, and Genentech guidelines
  • Collaborate with field partners and internal stakeholders to shape and execute local medical strategies
  • Provide congress and conference support, competitive intelligence, medical booth support, and related activities
  • Capture and share customer insights through CRM systems and cross-functional collaboration
  • Assist with Phase I–IV clinical trials, health economic outcomes research, and therapeutic-area medical collaborations
  • Support clinical trial site selection, start-up, recruitment, retention, and performance monitoring
  • Collaborate with CRO personnel as appropriate
  • Support development and management of clinical and scientific communications, publications, conference data, educational materials, and internal training materials
  • Ensure goals, objectives, KPIs, projects, and other work are completed on time, with high quality, and within budget

Requirements

What you’ll need
  • Advanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.)
  • BSN with extensive field medical experience with a pharmaceutical company
  • Minimum of 5 years related work experience (clinical, managed care, or industry experience)
  • Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)
  • Relevant therapeutic area knowledge
  • Comprehensive understanding of product and safety profiles
  • Familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry
  • 2+ years' experience in therapy area strongly preferred
  • In-depth knowledge of clinical development programs and clinical trial management
  • Prior experience working in heavily matrixed organizations interfacing with clinical operations, clinical development and medical affairs organizations
  • Applicants should reside within 30 miles of a major airport and within 50 miles of the established territory
  • Ability to travel by air or car for regular external business meetings and intermittent internal company meetings, up to 70% of time
  • Eligibility to drive a company vehicle; motor vehicle record may be checked

Benefits

Comp & perks
  • Discretionary annual bonus may be available based on individual and Company performance
  • Benefits detailed at the provided link
  • Company-provided car for essential duties and responsibilities