Minnesota
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Onsite
Job description
Job Summary
The Senior Clinical Research Associate for Oncology at Worldwide Clinical Trials will play a pivotal role in enhancing the quality of life for patients through rigorous clinical research. This position is based in Minnesota and requires an onsite presence. The ideal candidate will be part of a global team dedicated to advancing healthcare and achieving excellence in clinical trials.
Responsibilities
- Conduct comprehensive monitoring of clinical trial sites to ensure compliance with study protocols, regulatory requirements, and standard operating procedures.
- Collaborate with investigators and site staff to facilitate the smooth execution of studies.
- Evaluate and manage site performance by providing timely feedback and assistance to clinical sites.
- Develop and maintain strong relationships with site personnel to enhance trial processes.
- Participate in training new staff and contributing to study-related documentation and reporting.
Qualifications
- A bachelor’s degree in a relevant field or a nursing degree.
- Demonstrable experience in oncology clinical research.
- Strong understanding of clinical trial regulations and guidelines.
- Excellent communication and interpersonal skills to effectively engage with diverse stakeholders.
- Ability to work independently as well as collaboratively within a team environment.
Worldwide Clinical Trials provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
