Research Associate

SoTalent; Île-de-France; Hybride; EUR 52 000 - 70 000; Plein temps

Résumé du poste

SoTalent in France seeks a Clinical Research Associate to join a dedicated sponsor team and manage site monitoring activities across France. You will work within Oncology, Neurology, Immunology or Diabetes protocols for a major pharmaceutical sponsor.

This permanent, full-time role offers flexible arrangements with office or home-based locations and a clear path for professional growth. Expect national travel and close collaboration with a line manager to ensure delivery excellence.

Qualifications

• Two years of independent on-site monitoring experience.
• Ability to manage multiple protocols across indications.
• Expert knowledge of Good Clinical Practice guidelines.
• Willingness to travel nationally.
• Fluency in French and English.

Responsabilités

• Execute site management and monitoring tasks across France.
• Collaborate with clinical sites to implement patient recruitment strategies.
• Deliver protocol-specific training to site staff.
• Document monitoring reports and action plans.
• Mentor and train junior staff when required.

Connaissances

GCP knowledge

Site monitoring

Clinical research

Travel willingness

Formation

Life Sciences degree

Nursing background

Description du poste

Career Opportunity Clinical Research Associate France

I am currently representing a premier global clinical solutions provider seeking a dedicated Research Associate to join their specialist functional services division. This is a unique opportunity to work exclusively with a single major pharmaceutical sponsor while enjoying the robust career infrastructure of a top tier global organization.

This position is ideal for an experienced clinical professional who wants to become a subject matter expert in specific therapeutic areas. Unlike traditional multi sponsor roles this model allows you to integrate deeply into the sponsors pipeline using their specific processes and protocols to ensure continuity and excellence in delivery.

Competitive salary and comprehensive benefits package

Flexible working arrangements with options for office based or home based locations in cities including Bordeaux Lille Lyon Nantes or Marseille

Consistent workload and team stability

Clear pathways for professional growth and internal promotion

Exposure to innovative pharmaceutical developments at the cutting edge of medicine

Full time permanent contract

Dedicated focus on a single sponsor partnership

Management of approximately fifteen sites

Assigned to two or three protocols typically within Oncology Neurology Immunology or Diabetes

Expected site presence of six to nine days per month depending on project needs

Significant reduction in travel due to the implementation of risk based and remote monitoring strategies

Direct support from a dedicated line manager

Primary Responsibilities

Executing site management and monitoring tasks throughout France

Collaborating with clinical sites to implement and track patient recruitment strategies

Delivering protocol specific training to site staff

Documenting site activities through comprehensive monitoring reports and action plans

Mentoring and training junior staff members when required

Candidate Requirements

Degree in Life Sciences or a background in professional nursing

Minimum of two years of independent on site clinical monitoring experience

Demonstrated ability to manage multiple protocols across various indications

Expert knowledge of Good Clinical Practice guidelines

Willingness to travel nationally as required

Valid and clean French driving license

Full professional fluency in both French and English with strong communication and presentation skills

If you are looking to advance your career by leveraging advanced data tools and efficient site selection methodologies to drive clinical performance we want to hear from you.