Clinical Research Coordinator Job at IQVIA, France | Life Sciences | Apply Now
If you are a life sciences professional or experienced research nurse looking to step into a targeted, site-based trial operations role, this part-time position at IQVIA is an outstanding opportunity. Located on-site in the historic city of Bordeaux, France, this role embeds you directly within the active clinical site team. For structured coordinators searching for a high-impact Clinical Research Coordinator Job, this short-term assignment provides focused, hands-on experience in study management and patient data verification. It serves as an excellent accelerator for a long-term IQVIA Career and stands out as a premium choice for anyone seeking a localized Life Sciences Job.
- Job Position: Clinical Research Coordinator – Bordeaux
- Location: Bordeaux, France
- Job ID: R1548027
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company focuses on creating intelligent connections across 100+ countries to accelerate the development and commercialization of innovative medical treatments, ultimately improving global patient outcomes. By building an IQVIA Career, you join an industry-leading network celebrated for its scientific excellence, strict data integrity standards, and dedicated site support frameworks.
Clinical Research Coordinator Job – Key Responsibilities
As a Clinical Research Coordinator, you will perform a variety of administrative and clinical tasks under the delegation of the Principal Investigator to ensure the safe, smooth execution of the trial protocol.
Your day-to-day site and data management duties will include:
- Patient Advocacy & Safety: Safeguarding the physical and emotional well-being of trial participants, acting as a direct patient advocate, and addressing safety concerns.
- Clinical Set-Up & Triage: Performing patient vital sign checks, documenting findings, preparing and labeling specimen collection tubes, and maintaining site supply inventories to advance this Clinical Research Coordinator Job.
- Database & Document Control: Maintaining up-to-date study protocols, entering case data into Electronic Data Capture (EDC) systems, and conducting data quality checks to resolve sponsor queries.
- Logistical Coordination: Managing the custody and tracking of study medications according to site SOPs, organizing trial scheduling, and coordinating with external study monitors to smooth out this Life Sciences Job.
- Enrollment Support: Assisting with local participant recruitment, screening, and onboarding orientation in strict accordance with the primary study protocol.
Qualifications & Requirements For Clinical Research Coordinator Job
This position is tailored for clinical professionals who excel at balancing patient interaction with rigorous regulatory documentation.
- Educational Foundation: A Bachelor of Science (BS) or Bachelor of Arts (BA) degree in life sciences, or equivalent education and relevant clinical work experience.
- Professional Experience: Proven experience in a clinical or medical setting (e.g., as a Clinical Research Coordinator, Research Nurse, Medical Assistant, or Site Research Assistant) is required for this Life Sciences Job.
- Technical Knowledge: Deep working familiarity with clinical trial methodologies, study schedules, informed consent forms, and standard operating procedures (SOPs).
- Software Proficiency: Strong IT skills, including direct experience with MS Windows and the Microsoft Office suite (Access, Outlook, Excel, Word), alongside data entry tracking databases.
- Core Competencies: Exceptional interpersonal communication habits, strong organizational abilities, and close attention to detail.
- Logistics & Schedule: Part-time commitment of 20 hours per week for a fixed 6-month duration on-site in Bordeaux, France (Field-based classification).
In short, this Clinical Research Coordinator position at IQVIA is a definitive, fast-paced route to mastering site-level operations, patient logistics, and clinical data tracking. Securing this short-term role allows you to deploy your life sciences background to accelerate clinical deliverables within a highly prestigious network. If you possess a sharp eye for document compliance, hold a relevant scientific background, and are ready for a part-time role in Bordeaux, apply today to secure this premier Clinical Research Coordinator Job and advance your future IQVIA Career.
