Medical Monitor: Early Stage Biotech (EU)
50302
Posted: 19/01/2026
- EU, United States
- Permanent
Medical Monitor: Early Stage Biotech (EU)
Full‑time, Permanent
The role:
An innovative, fast‑growing biotech has partnered with Barrington James and is seeking a Medical Monitor to support its expanding early‑phase clinical pipeline. This is an opportunity to join a science‑driven organization where medical input shapes program direction. You will work closely with cross‑functional teams and play a central role in ensuring patient safety, study integrity and high‑quality clinical execution.
Key Responsibilities:
➢ Lead medical oversight for ongoing Phases 1&2
➢ Evaluate safety data, including AEs, SAEs, protocol deviations.
➢ Function as the primary medical contact for CRO partners, investigators and sites.
➢ Play a key role in protocol development, study design discussions, and medical sections of regulatory documents.
➢ Collaborate on medical review meetings, safety committees, and cross‑functional study teams.
➢ Support risk–benefit assessments, data interpretation, and clinical decision‑making.
➢ Validate studies adhere with GCP, ethical standards, and internal governance.
Qualifications:
➢ Medical degree (MD or equivalent).
➢ Demonstrated experience in clinical development, medical monitoring, or drug safety within biotech, pharmaceutical, or CRO environments.
➢ Ability to collaborate effectively with cross‑functional teams in an Innovative and rapidly scaling environment.
➢ Strong understanding of early‑phase trials, patient safety, and clinical data review.
➢ Conveys ideas with confidence and clarity with investigators, regulators, and internal stakeholders.
➢ A proactive, intellectually curious approach with a strong commitment to advancing innovative therapeutic solutions.
If you’re looking for a role where your medical judgement directly influences outcomes, drives breakthroughs, and transforms lives, this is your next step.
Full‑time, Permanent
The role:
An innovative, fast‑growing biotech has partnered with Barrington James and is seeking a Medical Monitor to support its expanding early‑phase clinical pipeline. This is an opportunity to join a science‑driven organization where medical input shapes program direction. You will work closely with cross‑functional teams and play a central role in ensuring patient safety, study integrity and high‑quality clinical execution.
Key Responsibilities:
➢ Lead medical oversight for ongoing Phases 1&2
➢ Evaluate safety data, including AEs, SAEs, protocol deviations.
➢ Function as the primary medical contact for CRO partners, investigators and sites.
➢ Play a key role in protocol development, study design discussions, and medical sections of regulatory documents.
➢ Collaborate on medical review meetings, safety committees, and cross‑functional study teams.
➢ Support risk–benefit assessments, data interpretation, and clinical decision‑making.
➢ Validate studies adhere with GCP, ethical standards, and internal governance.
Qualifications:
➢ Medical degree (MD or equivalent).
➢ Demonstrated experience in clinical development, medical monitoring, or drug safety within biotech, pharmaceutical, or CRO environments.
➢ Ability to collaborate effectively with cross‑functional teams in an Innovative and rapidly scaling environment.
➢ Strong understanding of early‑phase trials, patient safety, and clinical data review.
➢ Conveys ideas with confidence and clarity with investigators, regulators, and internal stakeholders.
➢ A proactive, intellectually curious approach with a strong commitment to advancing innovative therapeutic solutions.
If you’re looking for a role where your medical judgement directly influences outcomes, drives breakthroughs, and transforms lives, this is your next step.
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