Senior CRA

ICON Strategic Solutions; France; À distance; EUR 45 000 - 60 000; Plein temps

Résumé du poste

A global healthcare organization is seeking a Senior CRA based in France to oversee site management and ensure successful study execution. You will work remotely and need a minimum of 2 years' experience in CRO or Pharma/Biotech. Ideal candidates have strong communication skills and fluency in French. Competitive salary and a range of benefits are included.

Prestations

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum 2 years' experience as a CRA in pharmaceutical/Biotech or CRO.
• Ability to work well in a dynamic environment.
• Strong communication skills.

Responsabilités

• Full ownership of investigator sites for assigned studies.
• Planning and conducting site visits in accordance with the clinical monitoring plan.
• Developing effective relationships with investigator site staff.

Connaissances

Fluency in French

Strong IT skills

Excellent organization skills

Strong communication

Ability to multitask

Description du poste

Senior CRA - France - Remote

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

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

You will demonstrate, minimum 2 years' experience independent external monitoring of commercial studies within CRO or Pharma/Biotech companies.

Could be Homebased in Paris, Lyon, Montpellier.

CAR T-cell, Radioligand, Neurology, Immunology, Rhumatology, Oncology, Pediatric

I-II-III

What you will be doing:

• 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 2 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.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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