Junior Clinical Research Associate

University Positions; Provence-Alpes-Côte d'Azur; Sur place; EUR 35 000 - 55 000; Plein temps

Résumé du poste

An established industry player offers an exciting opportunity for a Clinical Research Associate to contribute to the development of pharmaceuticals and medical devices. This role involves conducting site visits, ensuring compliance with protocols, and collaborating with medical professionals. Ideal for those with a Bac+5 in Pharmacy or related fields, this position provides comprehensive training and the chance to travel across France. Join a passionate team dedicated to making a difference in patients' lives and be part of a mission that has positively impacted countless individuals over the past 30 years.

Qualifications

• Bac+5 in Pharmacy or related field required.
• Fluency in French and English is a must.

Responsabilités

• Conduct site visits in compliance with approved protocols.
• Communicate with medical site staff and verify qualifications.
• Complete monitoring reports and ensure compliance.

Connaissances

Communication Skills

Detail-oriented

Time Management

Fluency in French

Fluency in English

Formation

Bac+5 in Pharmacy

Degree in Health or Science Related Field

Description du poste

The Clinical Research Associate - L'attaché(e) de recherche clinique 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 pharmaceuticals 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. Backgrounds of individuals who have succeeded in the CRA role include:

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.

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;
• 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;
• Must be detail-oriented and efficient in time management.

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?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.