Medical Monitor (Oncology)
Job description
Medical Monitor (Oncology) role providing medical oversight and expertise across global oncology clinical trials, working with sponsors, investigators, sites and project teams. The position supports participant safety and scientific quality in trial delivery.
At a glance
- Employment
- Full-time
- Work mode
- Remote · Netherlands
- Languages
- English – full professional proficiency
What you'll do
- Serve as primary medical point of contact for clinical trial sponsors, internal project teams, investigators and trial sites for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines
- Provide medical oversight throughout the conduct of clinical trials, in accordance with the protocol, applicable regulations, and ICH-GCP requirements
- Respond to medical questions from investigators, sites, sponsors, project teams, and third-party vendors
- Provide medical input into eligibility assessments, protocol deviations, participant safety issues, and other trial-specific medical matters
- Contribute medical expertise to clinical development plans, protocols, investigator brochures, informed consent documents, annual reports, clinical study reports, patient narratives, and scientific presentations
- Review and assess clinical and safety data to support participant safety and identify medically relevant trends, risks, or quality concerns
- Prepare and deliver medical training and/or therapeutic area training to investigators and study teams
- Support medical data review activities and contribute to the assessment of aggregated clinical trial data
- Participate in bid defense meetings and proposal activities
- Provide support with Pharmacovigilance activities
- Identify medical trial risks, and collaborate with relevant functions to define appropriate mitigation and escalation measures
- Support or participate in advisory boards, safety monitoring boards, and other medical or scientific committees, as applicable
- Help ensure that trial conduct and medical oversight activities comply with the approved protocol, applicable regulatory requirements, and quality standards
What we're looking for
- Medical Doctor degree
- Board certification in Oncology
- Previous experience as a practicing Oncologist
- Full professional proficiency in written and spoken English
- Strong medical judgement, analytical thinking, and attention to detail
- Clear communication and presentation skills, with the ability to explain complex medical information to different stakeholders
- A collaborative and solution-oriented approach to working within international, cross-functional teams
- Proficiency in Microsoft Office applications and confidence working with clinical trial systems and digital collaboration tools
Nice to have
- Previous experience in clinical research or the pharmaceutical or CRO industry
Your team
Medical Monitoring team
An international team of medical professionals working at the frontline of clinical research.
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About PSI CRO
A leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry
PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Originated in Switzerland, PSI is known for being highly selective about the projects it undertakes and for delivering high-quality, timely services across a broad spectrum of therapeutic indications.
Key facts
- Switzerland
- Contract Research Organization (CRO)
- 30 years of experience in the pharmaceutical industry
- Privately owned, full-service CRO
- Global reach, supporting clinical trials across multiple countries and continents
- Highly selective about the projects undertaken
What they value
- High-quality, timely services
- Inclusive culture