TA Business Partner
- Icon Strategic Solutions
About the role
We are always on the lookout for motivated, reliable, and dedicated CRAs with at least 12 months of independent external monitoring experience on commercial studies (or a mix of commercial clinical trials), ideally in Oncology and Hematology. Experience in other therapeutic areas is also valued, especially if gained in Phase I - III commercial trials.
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 shared goal of bringing life-improving drugs to market. You will have the opportunity to lead by example, set standards of excellence, and enjoy a rewarding career in our exclusive programs.
We are currently seeking a CRA based in one of the following locations (home-based):
- Dijon
- Bordeaux
- Villejuif/Paris
- Besançon
- Saint-Herblain
- Rouen
- Toulouse
- Rennes
- Poitiers
- Saint-Mandé/Paris
Key Responsibilities:
- Take full ownership of investigator sites for assigned studies, managing the site from start to close-out.
- Plan and conduct site visits (feasibility, site selection, interim, and close-out) in line with the clinical monitoring plan.
- Build and maintain effective relationships with investigator site staff to ensure key clinical metrics are met.
- Prepare for and attend investigator meetings, coordinate the timely shipment and proper storage of clinical supplies, and follow-up on drug safety issues.
- Ensure the integrity of clinical data, maintaining site tracking records and adhering to relevant guidelines.
What You Need:
- Experience as a CRA, with previous work in Oncology trials within the pharmaceutical industry or a CRO.
- Excellent organizational skills with the ability to manage multiple priorities.
- Ability to thrive in a dynamic environment, adjusting to changing business needs.
- Strong IT skills and the ability to multitask and work under pressure.
- Strong communication skills with a proactive approach to problem-solving.
- Fluency in French and professional proficiency in English.
Why Join ICON?
Our Clinical Operations team is second to none. At ICON, you will receive the support you need to grow both personally and professionally in a dynamic environment where your contributions truly matter. Our team works together to solve challenges, build strong site relationships, and achieve our shared goals. As a CRA, you will play a key role in our clients' drug development processes as part of a global study team.
Ready to make a difference? Apply today and take the next step in your career with ICON!
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At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
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Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
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Our PeopleContent type
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05/23/2023
Summary
How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to excell
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A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?
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Suzaita Hipolito
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