Senior Clinical Trial Specialist
Há 2 dias
As a Clinical Research Associate, you play a vital role in the execution of clinical trials. Your expertise is crucial in ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Key Responsibilities:- Conduct site qualification, initiation, monitoring, and close-out visits to guarantee adherence to established protocols.
- Collaborate with investigators and site staff to facilitate seamless study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Bachelor's degree in a scientific or healthcare-related field preferred.
- Minimum of 2 years of experience as a Clinical Research Associate (on-site monitoring experience required).
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organisational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
We offer a range of benefits to support your well-being and work-life balance, including annual leave entitlements, health insurance offerings, competitive retirement planning, and more.
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