Senior Clinical Research Associate

University Positions; Bordeaux; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

An established industry player is seeking a dedicated Senior Clinical Research Associate to manage investigator sites and ensure the integrity of clinical data. This role offers the chance to work with a global pharmaceutical leader, contributing to the development of life-improving drugs. You will have full ownership of your assigned studies, engaging with site staff and ensuring compliance with clinical protocols. Join a dynamic team that values innovation and collaboration, where your contributions will make a significant impact in the clinical research field.

Qualifications

• 3+ years of experience as a CRA in the pharmaceutical industry or CRO.
• Strong organizational and multitasking skills in a dynamic environment.

Responsabilités

• Manage investigator sites from initiation to close-out.
• Conduct site visits and ensure adherence to clinical guidelines.
• Develop relationships with site staff to meet clinical metrics.

Connaissances

Clinical Research

Site Management

Communication Skills

Organizational Skills

Fluency in French

Professional Proficiency in English

Description du poste

We are looking for motivated, reliable, and dedicated CRAs with at least 3 years of independent external monitoring of commercial studies.

Experience in Diabetes / Obesity, Cardiovascular, Chronic Disease, or Rare Diseases, especially in phases I-II-III, is an asset.

As a Clinical Research Associate, you will be dedicated to our global pharmaceutical sponsor, a leader in the pharma industry. We share a culture of innovation, flexibility, and a common vision of bringing life-improving drugs to market. This role offers the opportunity to set the standard of excellence and enjoy a challenging career in this exclusive program.

Key Responsibilities :

• Full ownership of investigator sites for assigned studies, managing the site from initiation to close-out.
• Planning and conducting site visits (feasibility, site selection, interim, and close-out) in accordance with the clinical monitoring plan.
• Developing effective relationships with investigator site staff to meet key clinical metrics.
• Preparing for and attending investigator meetings, coordinating the shipment and proper storage of clinical supplies, and following up on drug safety issues.
• Ensuring the integrity of clinical data through diligent site tracking and adherence to guidelines.

Requirements :

• A stable experience (+3 years) as a CRA within the pharmaceutical industry or a CRO.
• Excellent organizational skills.
• Ability to work well in a dynamic environment, prioritize tasks, and respond to the changing needs of the business.
• Strong communication skills, with the ability to multitask and work effectively under pressure.
• Fluency in French and professional proficiency in English.

Our Clinical Operations team is second to none. You will receive the support needed to develop personally and professionally, working in an environment where you matter. Our team pushes forward together, united in solving problems, developing close site relationships, and achieving our goals. As a key part of a global study team, the CRA plays a fundamental role in our clients' drug development processes.

If you are a senior CRA with a passion for clinical research and meet these qualifications, we would love to hear from you.

Senior Clinical Research Associate • Bordeaux