Clinical Associate
hace 4 semanas
Job Summary
We are seeking a Clinical Associate to support the design, implementation, and management of clinical trials at ICON Plc. As a Clinical Associate, you will play a pivotal role in ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Key Responsibilities
- Assist in the planning, execution, and monitoring of clinical trials.
- Coordinate study activities, including site initiation, patient recruitment, data collection, and monitoring visits.
- Collaborate with cross-functional teams to support the successful execution of clinical trials.
- Maintain comprehensive study documentation and records.
- Support study close-out activities, including data cleaning, analysis, and preparation of clinical study reports.
Requirements
- Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field.
- Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
- Strong organizational and time management skills.
- Excellent attention to detail and problem-solving abilities.
- Effective communication and interpersonal skills.
About ICON Plc
ICON Plc is a world-leading healthcare intelligence and clinical research organization. We are committed to fostering an inclusive environment that drives innovation and excellence.
What We Offer
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A diverse and dynamic work environment.
Equal Opportunities Employer
ICON Plc is an equal opportunities employer and is committed to providing a workplace free of discrimination and harassment.
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