Clinical Research Associate

il y a 1 semaine

Strasbourg, Grand Est, France Pharmiweb Temps plein

Unlock your career in clinical research with ICON plc, a world-leading healthcare intelligence and clinical research organisation. As a Clinical Research Associate - Oncology Study Coordinator, you will play a vital role in our clients' drug development processes.

About ICON

At ICON, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life.

Job Description

This role offers an excellent opportunity to work as a key part of a global study team, dedicated to one of our global pharmaceutical clients focused on oncology studies. Your responsibilities will include:

  • 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.

Requirements

To succeed in this role, you should have:

  • Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
  • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
  • You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
  • A Life Science Degree or Master (master level preferred) Previous experience working within Oncology is preferred.
  • Good (native fluency) level of English and French We are happy to review applications based anywhere in France with a preference for the Lyon area.
About the Role

The salary for this role is estimated at €55,000-€65,000 per annum, depending on experience. This comprehensive and competitive total reward package comprises not only an excellent level of base pay but also a wide range of variable pay and recognition programs.

Why Choose ICON?

Our focus is to provide you with a supportive and inclusive workplace culture. We are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment.

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