Senior Clinical Research Associate
Il y a 2 mois
Experience in Diabetes/Obesity, Cardiovascular, Chronic Disease, or Rare Diseases, especially in phases I-II-III, is an asset.
As a Clinical Research Associate, you will be dedicated to our global pharmaceutical sponsor, a leader in the pharma industry. We share a culture of innovation, flexibility, and a common vision of bringing life-improving drugs to market. This role offers the opportunity to set the standard of excellence and enjoy a challenging career in this exclusive program.
Key Responsibilities:
- Full ownership of investigator sites for assigned studies, managing the site from initiation to close-out.
- Planning and conducting site visits (feasibility, site selection, interim, and close-out) in accordance with the clinical monitoring plan.
- Developing effective relationships with investigator site staff to meet key clinical metrics.
- Preparing for and attending investigator meetings, coordinating the shipment and proper storage of clinical supplies, and following up on drug safety issues.
- Ensuring the integrity of clinical data through diligent site tracking and adherence to guidelines.
Requirements:
- A stable experience (+3 years) as a CRA within the pharmaceutical industry or a CRO.
- Excellent organizational skills.
- Ability to work well in a dynamic environment, prioritize tasks, and respond to the changing needs of the business.
- Strong IT skills.
- Strong communication skills, with the ability to multitask and work effectively under pressure.
- Fluency in French and professional proficiency in English.
Our Clinical Operations team is second to none. You will receive the support needed to develop personally and professionally, working in an environment where you matter. Our team pushes forward together, united in solving problems, developing close site relationships, and achieving our goals. As a key part of a global study team, the CRA plays a fundamental role in our clients' drug development processes.
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