Junior Clinical Research Associate

Translational Research in Oncology; Paris; Hybride; EUR 45 000 - 53 000; Plein temps

Avantages offerts par ce poste

Five weeks vacation

Health & Life Insurance

Flexible working hours

Home office allowance

Luggage allowance

Mobile phone allowance

Résumé du poste

Translational Research in Oncology (TRIO) is seeking a Junior Clinical Research Associate to join the Monitoring Resources team. This home-based role in France reports to a CRA Line Manager and offers opportunities in oncology trials. You will conduct site visits, ensure regulatory compliance, perform source data verification, and assist with data validation.

Travel up to 60% is expected. A science-related bachelor, fluency in French and English, and knowledge of ICH-GCP are required, with a

Qualifications

• Fluent in French and English required.
• Completion of a science-related Bachelor’s degree.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCP knowledge and regulatory awareness.
• Experience with regulatory documents and site management a plus.

Responsabilités

• Perform site visits (pre-study, initiation, monitoring, termination) and ensure regulatory compliance.
• Conduct source data verification (CRFs) and resolve queries to ensure data quality.
• Ensure SAE reporting per project specifications and timelines.
• Respond to site requests quickly and assist with data validation and audits as needed.
• Support CAPA activities and corrective action/preventive action implementations.

Connaissances

French fluency

English fluency

ICH-GCP knowledge

Clinical monitoring process

Data quality and SDV

Travel readiness

Regulatory compliance

Formation

Science-related Bachelor’s degree

Outils

Clinical trial information systems

Description du poste

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!

Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is looking for a Junior Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in France.

Responsibilities:

• Conducting site visits, including pre-study, initiation, monitoring and termination;


• Confirming adherence to all FDA, ICH-GCP and local regulations;


• Ensuring the completion and collection of regulatory documents;


• Perform source document verification, validate Case Report Forms (CRFs) and perform
  queries resolution in a timely manner to ensure clean data availability for studies
  analyses


• Ensure Serious Adverse Event (SAE) reporting according to project specifications


• Respond to requests from clinical study sites in a timely fashion


• Assisting with data validation and query resolution;


• Assist during on-site audits (if required) and preparation of site audit report reply. Assist
  with the implementation of corrective actions/preventive actions, when appropriate

Qualifications:

• Less than 2 years experience as CRA in the field; or strong experience as Research
  Nurse or Study Coordinator in oncology


• Oncology and local regulatory requirements knowledge would be a major asset


• Fluent in French and English


• 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

What TRIO Can Offer You:

• Competitive salary


• 5 weeks of vacation plus paid Christmas Closure


• Health& Life Insurance premiums respectively paid 50% & 100% by TRIO


• Flexible working hours


• Home office allowance


• Luggage allowance


• Mobile phone allowance

Pay Range: 45,000.00 to 52,500.00 Euro - Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

This position will be open until Friday, August 28, 2026.

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.

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