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Clinical Research Associate
2 months ago
Job Summary: We are seeking an experienced Clinical Research Associate to join our team at ICON, a world-leading pharmaceutical company. As a Clinical Research Associate, you will be responsible for performing all aspects of CRA duties from site selection to site routine monitoring visits and close-out visits.
Key Responsibilities:
- Perform site selection, site initiation, and site routine monitoring visits and close-out visits (on-site and remote) and database lock.
- Work closely with our client's study team and have a dedicated ICON functional manager to support you.
- Oversee all aspects of study site management to ensure high-quality data resulting in consistently low query levels and good Quality Assurance reports.
Requirements:
- Degree in Pharmacy or any related course.
- 2+ years prior monitoring experience with global trials within CRO or pharmaceutical company.
- Excellent written and verbal communication skills.
- Strong knowledge of international guidelines ICH-GCP, as well as local regulations.
- Flexibility to travel and work from the sponsor office for around 3 days/week (if not traveling).
What We Offer:
- Competitive salary and benefits package.
- Opportunity to work with a world-leading pharmaceutical company.
- Chance to make a positive impact in the therapeutic areas of cancer, cardio-metabolic, vaccines, and oncology.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals.
- Life assurance and flexible country-specific optional benefits.
About ICON:
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation.