Entry Level

Job Summary:
The Clinical Research Associate at Medpace is offering the unique opportunity to have an
**exciting career** in the research of drug and medical device development. For those with
**medical and/or health/life science interest and background** who want to explore the research field,
**travel throughout 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 varied backgrounds in medical and other science-related healthcare fields.

**_
PACE_**
**- MEDPACE CRA TRAINING PROGRAM**

No clinical experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our
_PACE _Training Program, you will join other
**P**rofessionals
**A**chieving
**C**RA
**E**xcellence:

- _ 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.

**UNEXPECTED REWARDS**

This role will allow you to make a difference on a large scale through the enhancement 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 opportunity for significant travel bonus.

Responsibilities:
As a CRA, you will specifically be responsible for the following:

- Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
- Verifying 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;
- 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;
- Assessing 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:

- Must have a minimum of a university degree in a health or life science related field;
- Approximately 60-80% travel;
- Proficient knowledge of Microsoft® Office and general computer literacy;
- Outstanding communication and Presentation skills;
- Must be detail-oriented and efficient in time management; and
- Excellent verbal and written communication skills in English and French.

Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?:
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.