About the Role
As a Clinical Site Lead for a pharmaceutical company, you will make an impact by driving end-to-end clinical study execution, operational excellence, and site management across multiple therapy areas — ensuring compliance with both local French regulations and international standards. You will be a valued member of the Clinical Operations team and work collaboratively with Site Operations, Study Management, and cross-functional stakeholders throughout the full study lifecycle, from startup through closeout.
In this role, you will:
- Serve as the primary point of contact — internally and externally — for assigned investigational sites, building trusted relationships with investigators and coordinating all aspects of site startup, enrollment, and closeout.
- Monitor clinical studies at sites to ensure compliance with applicable regulatory requirements, Good Clinical Practice (GCP), and data accuracy standards, including initiation, periodic, and closeout visits.
- Lead site compliance and quality activities, including Key Compliance Indicator reporting, audit support, root cause analysis, issue resolution, and timely reporting of adverse events, device complaints, and protocol deviations.
- Develop and implement site-specific enrollment strategies, identifying and qualifying appropriate investigators and collaborating with Site Operations teams to ensure activation and enrollment within defined timelines.
- Train and continuously coach site personnel on study protocol requirements and local regulations, while providing regular progress updates to Clinical Operations and Study Management and supporting site budget and contract discussions.
Work Model
We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role's business requirements, this is a field-based hybrid position requiring regular travel to clinical sites across France and internationally. Regardless of your working arrangement, we are here to support a healthy work-life balance through our various wellbeing programs.
The working arrangements for this role are accurate as of the date of posting. This may change based on the project you're engaged in, as well as business and client requirements. Rest assured — we will always be clear about role expectations.
What You Need to Have to Be Considered
- Background in engineering, science, health science, nursing, or a related field — or equivalent experience in cardiology or clinical research
- Confirmed experience in clinical research and/or clinical site management, out of which a minimum of 4 years of experience in driving clinical studies
- Expert knowledge of GCP and regulatory compliance guidelines for clinical trials, including applicable ISO standards and FDA regulations, combined with advanced understanding of clinical study design and outcomes research.
- Fluency in both French and English (written and verbal), with strong command of medical terminology and the ability to communicate effectively with site staff, investigators, and internal stakeholders.
- Proficiency in MS Office and clinical database systems (Oracle preferred), with strong organizational, prioritization, and time management skills.
- Demonstrated ability to work independently and collaboratively in a fast-paced, matrixed environment, and willingness to travel
We're excited to meet people who share our mission and can make an impact in a variety of ways. Don't hesitate to apply, even if you only meet the minimum requirements listed. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and exciting things to this role.
What We Offer
At Cognizant, we care about your wellbeing and your development. As part of our French team, you can expect:
- Complementary health insurance (mutuelle d'entreprise) with employer contribution
- ️ Meal vouchers (tickets restaurant)
- ️ RTT days (additional paid time off beyond statutory entitlement)
- Profit-sharing and participation (intéressement & participation) in line with company performance
- 50% reimbursement of public transport costs (Navigo or equivalent)
- Laptop and smartphone provided
- Access to continuous learning platforms and professional development resources
- A collaborative, international work environment with real opportunities for career growth
Over Cognizant
Cognizant (NASDAQ: CTSH) is een bouwer van AI-oplossingen en een leverancier van technologiediensten. Wij slaan de brug tussen AI-investeringen en ondernemingswaarde door het bouwen van full-stack AI-oplossingen voor onze klanten. Onze diepgaande kennis van sectoren, processen en engineering stelt ons in staat om de unieke context van een organisatie te verankeren in technologische systemen. Deze systemen versterken het menselijk potentieel, realiseren tastbare resultaten en geven wereldwijde ondernemingen een voorsprong in een snel veranderende wereld. Ontdek hoe op cognizant.ai of @cognizant.
Aanvullende arbeidsinformatie
De informatie over de beloning is correct op de datum van deze vacature. Cognizant behoudt zich het recht voor om deze informatie op elk moment te wijzigen, met inachtneming van de toepasselijke wetgeving.
Van sollicitanten kan worden verwacht dat zij gesprekken bijwonen, persoonlijk of via een videogesprek. Daarnaast kan van kandidaten worden gevraagd om tijdens elk gesprek een geldig, door de overheid uitgegeven identiteitsbewijs (zoals een identiteitskaart of paspoort) te tonen.
Cognizant is een werkgever die gelijke kansen biedt. Je sollicitatie en kandidatuur worden niet beoordeeld op basis van ras, huidskleur, geslacht, religie, levensovertuiging, seksuele geaardheid, genderidentiteit, nationale afkomst, handicap, genetische informatie, zwangerschap, veteranenstatus of enige andere eigenschap die wordt beschermd door federale, regionale of lokale wetgeving.
