Clinical Research Associate - Freelance (0.3 FTE)
TFS HealthScienceJobsCloseBy Editorial Insights
TFS HealthScience is seeking a Freelance Clinical Research Associate (0.3 FTE) for onsite work in Paris, dedicated to a single sponsor and responsible for initiation, on-site and remote monitoring, and study closeout under GCP and ICH guidelines. You will verify informed consent, review CRFs, ensure Investigational Product accountability, deliver Monitoring Visit Reports, maintain the Investigator Site File and eTMF, and support audits and inspections while keeping CTMS and related systems accurate. Requirements include a life sciences or nursing degree, 3+ years in clinical trials, strong GCP/ICH knowledge, and English fluency, with travel 60–80%. To apply, tailor your CV to highlight remote/on-site monitoring, eTMF/CTMS expertise, CAPA, sponsor collaboration, and travel readiness.
About this role
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.
The Clinical Research Associate is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements.
As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.
Key Responsibilities
Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations. Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
Review CRFs (electronic or paper) and subject source documentation for validity and accuracy.
Verify proper management and accountability of Investigational Product.
Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.
Providing site with the listing of issues identified during monitoring visit and action items which will need to be addressed in a timely manner.
Timely delivering site documents to eTMF or paper TMF; verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and ICH guidelines and local regulatory requirements.
Participate in audit and/or inspection, its preparation and follow-up activities, as needed.
Order, ship, and reconcile clinical investigative supplies for study sites, if applicable.
Update CTMS and all other required by projects systems with accurate site level information.
Qualifications
Bachelor’s Degree, preferably in life science or nursing; or equivalent.
Over 3 year of relevant clinical experience or relevant academic background around clinical trial or clinical development activities.
Understand basic medical terminology and science associated with the assigned drugs and therapeutic areas.
Possess the understanding of Good Clinical Practice regulations, ICH guidelines.
Fluent in English.
Ability and willingness to travel up to 60-80%, overnight and abroad if applicable.
What We Offer
We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.
Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.
A Bit More About Us
Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.