The employer is Clear and nothing is A concern, but one or two parts are Worth checking or Not known. It describes the role and the employer, not your chances.
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This role appears to map to SOC 2212 (Specialist medical practitioners), an eligible Skilled Worker occupation at RQF 6 or above under the rules in force on 9 November 2026.
PSI CRO UK Ltd holds a Skilled Worker licence with an A rating on our register, last checked 8 November 2026.
The advert does not mention sponsorship.
Checked 9 Nov 2026. General information about this role, its employer and the published rules, not advice about anyone's situation. Immigration rules change; check GOV.UK. For advice, use a regulated adviser: find one at https://www.gov.uk/find-an-immigration-adviser or a solicitor at https://www.sra.org.uk/consumers/register/.
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The employer is Clear and nothing is A concern, but one or two parts are Worth checking or Not known. It describes the role and the employer, not your chances.
Role Clear
This role appears to map to SOC 2212 (Specialist medical practitioners), an eligible Skilled Worker occupation at RQF 6 or above under the rules in force on 9 November 2026.
SOC 2212 · RQF _6_PLUS GOV.UK Pay Not known
The advert does not state a salary.
Employer Clear
PSI CRO UK Ltd holds a Skilled Worker licence with an A rating on our register, last checked 8 November 2026.
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The advert does not mention sponsorship.
Advert
Checked 9 Nov 2026. General information about this role, its employer and the published rules, not advice about anyone's situation. Immigration rules change; check GOV.UK. For advice, use a regulated adviser: find one at https://www.gov.uk/find-an-immigration-adviser or a solicitor at https://www.sra.org.uk/consumers/register/.
The advert has no salary. What pay do the rules need?
The advert doesn’t state a salary 1 , so ask the employer what the role pays before you apply.
- 1 Medical Monitor (Oncology) · PSI CRO · job advert
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About the role
Job Description
PSI is seeking a Medical Monitor (Oncology) to join our international Medical Monitoring team.
In this role, you will provide medical oversight and expertise across global clinical trials, working closely with study sponsors, investigators, sites, project teams, and other clinical research professionals. Your contribution will help protect participant safety, maintain scientific and medical quality, and support the successful delivery of oncology studies.
This is an opportunity to apply your clinical oncology experience to international research and contribute directly to the development of new treatments for patients who need them.
Full-time employment
Responsibilities:
- Serve as primary medical point of contact for clinical trialsponsors,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
- Prepares and delivers medical training and/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 withPharmacovigilance 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
Qualifications
You will be a strong fit for this role if you have
- Medical Doctor degree
- Board certification in Oncology
- Previous experience as a practicing Oncologist
- Previous experience in clinical research or the pharmaceutical or CRO industry is a plus
- 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.
Additional Information
As part of PSI's Medical Monitoring team, you will become part of an international team of medical professionals working at the frontline of clinical research. You will have the opportunity to apply your oncology expertise across global studies, collaborate with experienced colleagues, and contribute to bringing new treatment options to patients.
Company Description
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
Advert on SmartRecruiters · first seen 5 Nov 2026 · source
General information, not advice about your situation
Checks against the published rules. Only the employer decides whether to sponsor a role; for your own case, speak to a regulated adviser. Read the rule on GOV.UK
Medical Monitor (Oncology) in Oxford employer: Sponsor Finder
Assystem is an excellent employer, offering a dynamic work environment in Leiston, Suffolk, where innovation meets infrastructure. With a strong focus on employee growth and development, we provide opportunities for professional advancement while fostering a collaborative culture that values teamwork and creativity. Join us to be part of meaningful projects that make a real impact, supported by a team that prioritises your success and well-being.
