Senior Clinical Research Associate (Oncology) - Marseille/Aix-en-Provence, Franc
Parexel · France
Clinical Research
Remote
Nurse
Demand82
Career growth78
Healthcare fit80
Remote potential70
5-year outlook
Senior CRA roles in oncology are generally well compensated within clinical research, with growth tied to monitoring experience, oncology specialization, and CRO/sponsor seniority. This is not an entry-level salary path.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-11-06
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Profession fit
- Nurse
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians with oncology exposure and prior CRA, site coordination, or clinical trial experience who want a remote/hybrid CRO career. It is less suitable for clinicians without monitoring or GCP-based trial experience.
Who should apply
Oncology-trained doctors, nurses, pharmacists, or allied health professionals with CRA/monitoring experience, site coordination exposure, ICH-GCP knowledge, RECIST familiarity, French fluency, and willingness to travel to investigator sites.
CV angle
Frame real oncology clinical experience around trial protocols, patient safety, informed consent, source documentation, CRF/data verification, protocol deviation management, pharmacovigilance, site communication, and inspection readiness. Emphasize any GCP training, monitoring exposure, and corrective action plan involvement without overstating CRA experience.
Skills to highlight
- Oncology clinical trials
- ICH-GCP compliance
- RECIST criteria
- Source document review
- CRF/data verification
- Site monitoring
- Pharmacovigilance
- Protocol deviation and CAPA management
Role summary
A senior CRA role monitoring oncology clinical trial sites for Parexel in France, ensuring ICH-GCP compliance, patient safety, data integrity, informed consent, and inspection readiness through remote and on-site monitoring.
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