Clinical Research Associate-Freelance
Translational Research in Oncology
- Performing data verification of source documents;
- Conducting site visits, including pre-study, initiation, monitoring, and termination;
- Confirming adherence to all FDA, ICH-GCP, and local regulations;
- Ensuring implementation and compliance with FDA, and ICH-GCP guidelines
- Participating in budget negotiation and follow-up where applicable
- Assisting with data validation and query resolution
- Mentoring junior team members as required
- Ensuring the completion and collection of regulatory documents
- A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse;
- A minimum of 1 year of monitoring experience in an early-phase clinical trial;
- Experience in solid tumor trials, including breast, lung, gastric, ovarian, and/or pancreatic cancer, is preferred;
- Fluent English required; French is desirable
- Experience monitoring in phase I trials will be value
- Completion of a science-related Bachelor’s degree
- Excellent knowledge of medical terminology and clinical monitoring process
- Strong ICH-GCPs knowledge
- Experience with clinical trial information systems
- Ability to travel up to 60% on average
- Must be legally authorized to work in the country
Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.
Prior to applying please review TRIO's Applicant Information Notice
To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.Teamwork · Passion · Integrity · Innovation
$85.5k - $135.5k per year
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