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Clinical Research Collaboration Lead
Job Location:
Monthly Salary:
Posted:
21 August 2026 (15 days ago)
Posted:
Application Deadline:
18 November 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Carbyne is partnering with a globally recognized research organization to identify a Clinical Research Collaboration Lead to support international healthcare research focused on personalized preventive medicine and major non-communicable diseases.
The position will play a key role in the operational delivery of a multi-country longitudinal research initiative spanning diverse healthcare systems institutions clinical sites and infrastructure partners. Acting as the primary clinical operations link between the central sponsor team and local investigators clinical sites biorepositories and vendors the Clinical Collaboration Lead will provide hands-on oversight of study execution while building strong relationships across participating countries. Key areas of responsibility include country and site engagement study quality protocol adherence and the consistent delivery of high-quality cohort operations across international locations.
Responsibilities
The position will play a key role in the operational delivery of a multi-country longitudinal research initiative spanning diverse healthcare systems institutions clinical sites and infrastructure partners. Acting as the primary clinical operations link between the central sponsor team and local investigators clinical sites biorepositories and vendors the Clinical Collaboration Lead will provide hands-on oversight of study execution while building strong relationships across participating countries. Key areas of responsibility include country and site engagement study quality protocol adherence and the consistent delivery of high-quality cohort operations across international locations.
Responsibilities
- Build and maintain strong long-term relationships with investigators clinical sites and local research teams across participating countries.
- Act as a key clinical operations representative between the central sponsor organization and country-level partners.
- Provide oversight of study activities with particular focus on protocol compliance informed consent source documentation data integrity sample handling and overall execution quality.
- Support the development review and maintenance of clinical operations processes and essential study documentation at global and country level.
- Ensure local implementation is aligned with the study model applicable regulations ethical requirements and sponsor expectations.
- Identify operational risks and country-specific challenges coordinating appropriate solutions with central teams.
- Establish regular communication with investigators and site teams to understand recruitment retention operational performance and local requirements.
- Collaborate with scientific clinical data and operational stakeholders to share best practices and continuously improve study quality and delivery.
Requirements & Profile
- 5 years of clinical research operations experience ideally in roles such as CRA Clinical Trial Liaison Clinical Operations Specialist or similar.
- Hands-on experience with site management monitoring study coordination or sponsor oversight preferably within NCDs preventive medicine diagnostics or related research.
- Strong knowledge of GCP ethics regulatory requirements and clinical protocol implementation.
- Proven ability to work effectively with investigators and research teams across multiple countries and healthcare systems; experience with longitudinal or multi-country studies is a strong advantage.
- Familiarity with biobanking biospecimen logistics and data lifecycle processes is desirable; exposure to molecular/omics or data-driven healthcare is a plus.
- Degree in medicine life sciences public health nursing or a related field combined with strong communication stakeholder management problem-solving and organizational skills. Willingness to travel internationally is required.
Should you be interested in the opportunity please do not hesitate to submit your professional CV so we can contact you with further details!
