Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are looking for motivated CRA based in France area to join our dedicated CRA team!

You will demonstrate, minimum 3 years' experience independent external monitoring of commercial studies within CRO or Pharma/Biotech companies. 

Could be Homebased in Paris, Lyon, Montpellier

Therapeutic areas: CAR T-cell, Radioligand, Neurology, Immunology, Rheumatology, Oncology, Pediatric

Phase: I-II-III

What you will be doing:
 

As a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients, with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.

• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.

• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.

• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.

• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.

You will need:

• Minimum 3 years' experience as a CRA, this within the pharmaceutical/Biotech companies or a CRO

• Excellent organization skills

• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business

• Strong IT skills

• Strong communication with the ability to multitask and work effectively under pressure

• Fluency in French and professional proficiency in English

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply