Le poste
Junior Clinical Research Associate
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel in France, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!
Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields.
MEDPACE CRA TRAINING PROGRAM PACE® (Professionals Achieving CRA Excellence).
No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:
- PACE®provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- PACE®will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
WHY BECOME A CRA
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the improvement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Competitive pay and many additional perks unmatched by other CROs (SEE BELOW).
UNEXPECTED REWARDS
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the improvement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
- Mid-sized CRO where you are not just a number
- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic, medical and regulatory experts
- Internally designed proprietary Clinical Trial Management System – one stop shop for EDC, IWRS, regulatory portal, visits reports, and more
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Opportunity to work from home once job experience is gained
- Competitive pay.
Responsibilities:
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and
- 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:
- Bac+5 in Pharmacy or a health or science related field;
- Ability to travel 60-80% to locations nationwide is required;
- Must maintain a valid driver's license and the ability to drive to monitoring sites;
- Minimum 1 year healthcare-related work experience preferred;
- Fluent in French & English is a must;
- Strong communication and presentation skills; and
- Must be detail-oriented and efficient in time management.
Please apply via the link provided to our careers site.
Voir l'annonce sur le site de l'entreprise
L'entreprise
Medpace
Medpace is a global Clinical Research Organisation (CRO) partnering with leading pharmaceutical, biotech, and device companies to bring promising new drugs and devices to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide clients with exceptional support during the drug development process. We manage the full drug and device development process for our clients which includes many components: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and regulatory submissions.
Employing almost 6,000 people across 40+ countries, our people are our biggest asset and embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return, they are rewarded with interesting projects, career advancement, and recognition. Whether you are a recent graduate or seasoned in your field, your contributions can make an impact on our business.
