Experienced Clinical Research Associate - Various locations

WE OFFER THE FOLLOWING:

• Customized Fast PACE® CRA training program based on your experience and therapeutic background and interest
• User friendly CTMS with electronic submission and approval of monitoring visit reports
• Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
• National assignments with a very large pipeline of projects possibility
• In-house CTA administrative support for all levels of CRAs
• Close collaboration with CRA manager
• Opportunities to work with international project team
• Competitive travel bonus
• No metric for minimum required days on site per month
• Home office furniture allowance, mobile phone and hotspot for internet access anywhere
• For Home office CRA : monthly allowance in addition to the salary
• In-house travel agents and Per Diem allowance for all day on site
• Opportunity for transversal activity like CRA lead positions, mentoring, CRA evaluator, super users, SME role.
• Many additional perks unmatched by other CROs!
• Low turnover rates for CRAs
• Sign-on bonus eligible
• Possibility to be home based in various locations in France

• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significa
• Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communication with the medical site staff
• Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements
• Regulatory document review
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

• Experience as a Clinical Research Associate;
• Approximately 60-80% non-local, national travel is required;
• Must have a minimum of a bachelor’s degree in a health or science related field;
• Proficient knowledge of Microsoft® Office;
• Fluency in English and French;
• Outstanding communication skills; and
• Must be detail-oriented and efficient in time management.