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Medical Monitor - Bone-related diseases | Freelance (0.1–0.25 FTE)

Roles & Responsibilities

  • Medical degree (MD) with active medical license
  • Prior experience as Medical Monitor on interventional clinical trials
  • Familiarity with ICH-GCP, EU CTR, and pharmacovigilance requirements
  • Based in Europe and able to support 24/7 coverage

Requirements:

  • Provide medical oversight and 24/7 on-call medical coverage for investigator sites
  • Review and assess SAEs, protocol deviations, and eligibility queries
  • Support protocol interpretation, medical review of clinical data, and safety monitoring
  • Partner with the sponsor and clinical operations team on medical and scientific questions

Job description

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.

TFS HealthScience is seeking an experienced Medical Monitor (MM) to support a Phase 2a clinical study across multiple European sites. The role provides medical oversight and 24/7 on-call coverage from study start-up through close-out.

This is a part-time engagement (up to 0.3 FTE), offered through our Strategic Resource Solutions (SRS) model.

Responsabilities

  • Provide medical oversight and 24/7 on-call medical coverage for investigator sites

  • Review and assess SAEs, protocol deviations, and eligibility queries

  • Support protocol interpretation, medical review of clinical data, and safety monitoring

  • Partner with the sponsor and clinical operations team on medical and scientific questions

  • Contribute to safety reporting and medical sections of clinical documents

  • Train site staff on protocol-specific medical questions where required

Qualifications

  • Medical degree (MD) with active medical license

  • Prior experience as Medical Monitor on interventional clinical trials

  • Experience in rare disease and/or relevant therapeutic areas an advantage

  • Familiarity with ICH-GCP, EU CTR, and pharmacovigilance requirements

  • Based in Europe; able to support 24/7 coverage

  • Fluent English; additional European languages an asset

What We Offer

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

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