Georgia
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Onsite
Job description
Job Summary
As a Senior Clinical Research Associate specializing in Oncology at Worldwide Clinical Trials, you will be an integral member of a global team dedicated to advancing clinical research and improving patient outcomes. This role is based in Georgia and requires you to work onsite, contributing to the high standards of quality and excellence that define our organization.
Responsibilities
- Oversee and monitor clinical trials, ensuring compliance with regulatory requirements and study protocols.
- Collaborate with cross-functional teams to facilitate the smooth execution of clinical studies.
- Engage with investigative sites and manage relationships to enhance study performance.
- Conduct site visits, data verification, and documentation review to uphold data integrity.
- Provide training and support to site personnel on study-related activities.
Qualifications
- A minimum of a four-year degree in a relevant field or a nursing degree.
- Significant experience in Oncology clinical research.
- Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent communication and interpersonal skills, with an ability to work collaboratively.
- Proven organizational skills and the ability to manage multiple tasks effectively.
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.
