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 organization dedicated 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.
If you are interested, please submit your resume in English. We thank all candidates for their interest; only those selected for an interview will be contacted.
Less than 2 years as a CRA or strong oncology research nurse/study coordinator experience; science bachelor's degree, fluent French and English, ICH-GCP and clinical monitoring knowledge, and travel availability.
Key Responsibilities
- conducting site visits
- verifying documents
- resolving queries
Skills & Tools
FDA, ICH-GCP, Case Report Forms (CRFs)
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — France or Normandy or Île-de-France
- Salary: EUR 45,000 – 52,500 / year
- Languages: French, English
Benefits
- Generous paid time off
About Translational Research in Oncology
A global clinical research organization advancing translational cancer research through clinical trials. — Industry: Research and Development