Medical Scientist – 12-Month Fixed Term Contract (UK & Canada Only)
Updated: February 3, 2026
Location: London, United Kingdom / Canada (Applicants must be local with no sponsorship required)
Job ID: 25104918-OTHLOC-3526-2DR
Employment Type: Fixed-Term Contract – 12 Months (Renewable Based on Performance & Budget)
About the Role
Syneos Health is seeking a qualified Medical Scientist (MD) to join our clinical development teams on a 12-month fixed-term contract. This role is open exclusively to candidates based in the UK or Canada and requires at least 2 years of direct patient care experience post-residency.
The Medical Scientist will collaborate closely with Medical Directors, clinical operations, data management, pharmacovigilance, and project management teams to ensure high-quality medical data review, safety assessment, and eligibility verification across ongoing clinical trials. This is an opportunity to contribute to a patient-centric clinical development model while ensuring regulatory compliance and data integrity.
Key Responsibilities
Collaborate with Medical Directors to develop Medical Plans, including Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans.
Engage with external experts and advisors to acquire necessary medical/scientific input for plan development.
Conduct regular and ad-hoc medical review of clinical data, analyze trends, identify risks, and document findings.
Author, review, and approve medical data queries in collaboration with Medical Directors.
Assist in patient profile reviews, protocol deviation assessments, and preparation of Medical Review Summary reports.
Prepare materials and support medical data review and safety review meetings, including slide preparation.
Manage project scope, objectives, and quality of deliverables to meet study milestones and timelines.
Serve as primary liaison between internal teams, customers, and vendors for medical data and eligibility reviews.
Collaborate with cross-functional study teams to identify data integrity or patient safety risks, escalating issues as necessary.
Participate in Trusted Process meetings, internal audits, and potentially external audits.
Maintain up-to-date knowledge of protocol designs, disease-specific terminology, and pathology.
Adhere to ICH, GCP, and data privacy guidelines, as well as all enterprise and customer SOPs and work instructions.
Required Qualifications & Experience
Medical Degree (MD) is required.
Minimum 2 years of direct patient care experience post-residency.
Proven experience in medical data review, patient safety assessment, and clinical study support.
Strong understanding of scientific principles to perform high-quality medical data analysis.
Excellent written and verbal communication skills, with ability to convey complex medical data clearly.
Proficiency in MS Office (Word, Excel, PowerPoint) and other clinical software tools.
Ability to manage multiple tasks, meet deadlines, and adapt to changing project scopes in a dynamic, regulated environment.
Self-starter with problem-solving skills and the ability to escalate issues appropriately.
Knowledge of drug development processes and familiarity with ICH/GCP guidelines preferred.
Strong teamwork and interpersonal skills to work effectively within cross-functional teams.
Why Join Syneos Health
Syneos Health is a fully integrated biopharmaceutical solutions organization dedicated to accelerating the delivery of life-changing therapies worldwide. With 29,000 employees across 110 countries, our teams collaborate to deliver innovative solutions that positively impact patients’ lives.
We offer:
Career development and progression opportunities
Supportive leadership and peer recognition
Technical and therapeutic area training
A culture of inclusion where employees are encouraged to be their authentic selves
Additional Information
This job description provides a summary of responsibilities; additional duties may be assigned.
Equivalent combinations of education, skills, and experience will be considered.
Syneos Health is committed to equal employment opportunities and compliance with applicable labor laws and regulations.
Reasonable accommodations are provided to qualified individuals as required by law.
Job Summary:
This role is ideal for a Medical Scientist (MD) with clinical experience post-residency seeking to contribute to high-impact clinical trial projects in the UK or Canada on a fixed-term basis.aa
Gujarat :
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Delhi | India | New Delhi | PAN-India |Assam :
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Anchorage | Barrow | Bethel | Juneau | Sitka | Wrangell |Massachusetts :
Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Kentucky :
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Frank Scottile Blvd |Missouri :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Arkansas | Remote Australia |New South Wales :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Tallinn |Hà Nội :
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Japan | Saitama |Tokyo :
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Kyiv |Lima Region :
Lima |France :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
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