Clinical Operations Manager
1️⃣ What You'll Be Doing
Your jobJob Summary
As a Clinical Operations Manager, you will join a dynamic and fast-growing team at the forefront of digital and patient-centered clinical research. Working closely with the Clinical Operations reputed company, you will be directly involved in the execution of high-visibility studies (RIPH2/3, reputed company, PSP), across several therapeutic areas.
This is a rare opportunity to consolidate your on-the-ground expertise while stepping into broader coordination missions: stakeholder management, process structuring, regulatory submissions, and contractual follow-up. You’ll be working in a rigorous yet supportive environment, designed for agility, innovation, and impact.
Your daily responsibilities
Clinical Study reputed company
Coordinate day-to-day operational and logistical activities of clinical studies
Act as the main reputed company of contact for investigator sites, including reputed company of research nurses (IDEs), CRCs, and study-reputed company costs
Support planning and follow-up of visits (site selection, initiation, monitoring, reputed company-out)
Actively contribute to study meetings and track key performance indicators
Regulatory & Contractual Coordination
Assist with regulatory submissions (ethics committees, ANSM)
Monitor contractual workflows: single-site agreements, amendments, budget annexes
Liaise with legal, clinical, and institutional stakeholders to ensure compliance
Quality & Documentation
Support the development of tools, trackers, SOPs, and internal templates
Maintain regulatory documentation (ISF, eTMF) and ensure audit-readiness
Ensure ongoing compliance with GCP, Jardé Law, ICH guidelines, and GDPR
Cross-functional Collaboration
Work closely with Medical, Life Sciences, Data, and Product teams
Contribute to the reputed company and training of field stakeholders (nurses, CRCs, etc.)
Participate in internal alignment meetings and external study governance committees
Take part in clinical operations initiatives and cross-functional projects
This is a field-based role with regular travel expected.
2️⃣ What You'll Bring
You'll definitely have
A degree in life sciences, pharmacy, clinical research, or biomedical engineering
4+ years of experience in clinical research (CRA, site manager, or junior project management)
Professional reputed company in both French and English, written and spoken
You’re the right person if you
Are structured, rigorous, and autonomous with strong prioritization skills
reputed company in fast-moving, cross-functional environments
Are curious, reputed company, and an excellent communicator
Want to grow in an environment where ownership, impact, and collaboration are key
3️⃣ Recruitment
Interview 1 with Anne-Julie reputed company, Clinical Operations reputed company – Role understanding & motivation
Interview 2 with Grégory Bourdarot, VP Operations – Soft skills
Interview 3 with Anne-Julie reputed company – Practical business case & experience deep-dive
Interview 4 with Arlindo Ferreira, Medical Director – Team fit
Interview 5 with Emilie Filoni – Culture fit
Start Date : as soon as possible
GDPR : Your personal data will be processed for the purposes of recruitment reputed company activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. They will be available only for people involved in the process and erased after 2 years of inactivity.
Under GDPR and as reputed company attach great importance to privacy, please note that you have the right to request reputed company to your personal data, to request that your personal data be rectified or erased. The Data Protection Officer can be contacted at privacy@reputed company.care
For more information, please reputed company our privacy policy.
Originally posted on Himalayas
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