Senior Oncology Clinical Trial Specialist
Há 2 dias
Clinical Research Associate
Lead a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments.
Key Responsibilities- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- Must have experience monitoring oncology trials in phases I and/or II.
- West coast U.S. location preferred, but will consider mountain to central U.S.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
A competitive salary and a range of benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
- Annual leave entitlements
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
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