- Clinical research jobs
- Experienced Clinical Research Associate - Various locations
Experienced Clinical Research Associate - Various locations
Medpace Holdings, Inc.
France | France
Job Summary
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
Responsibilities
- 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
Qualifications
- 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.
Job posted: 2023-04-11