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Clinical Research Associate
1 month ago
Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for managing investigator sites for assigned studies, planning and conducting site visits, and developing effective relationships with investigator site staff.
Key Responsibilities:
* 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
Requirements:
* A first stable experience as a CRA, this within the pharmaceutical industry or a CRO (min 1 year)
* 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
About Us: 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.
