TA Business Partner
- Icon Strategic Solutions
About the role
We are seeking motivated, reliable, and dedicated Clinical Research Associates (CRAs) with at least 1 year of experience as a CRA within a CRO. Ideally, you should have experience in Oncology and Onco-Hematology, although other therapeutic areas will also be considered, 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, where we share a culture of innovation, flexibility, and a common vision to bring life-saving treatments to market. You will set the standard for excellence and enjoy a challenging and rewarding career within our exclusive programs.
We are currently looking for a CRA based in the Paris area, who is willing to travel to the Sponsor's office for study meetings and team meetings (around once a month).
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 accordance with the clinical monitoring plan.
- Build strong 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:
- At least 1 year of CRA experience within a CRO, ideally in Oncology and Onco-Hematology studies.
- Excellent organizational skills, with the ability to manage multiple priorities effectively.
- Ability to work well in a dynamic environment and respond to the changing needs of the business.
- Strong IT skills and the ability to multitask and work under pressure.
- Strong communication skills and the ability to work effectively with site staff and stakeholders.
- Fluency in French and professional proficiency in English.
- Willingness to travel to the Sponsor's office in Paris for study and team meetings (approximately once per month).
Why Join ICON?
At ICON, our Clinical Operations team is renowned for its excellence. You will receive the support and training you need to grow personally and professionally in an environment that values your contributions. Our team works closely together to solve challenges, build strong relationships, and drive success. As a CRA, you will play a crucial role in our clients' drug development processes as part of a global study team.
Ready to take the next step in your career? Apply today and become part of the ICON team!
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Impactful work. Meaningful careers. Quality rewards.
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
BlogsPublish date
05/23/2023
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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 exce

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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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