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Clinical Research Coordinator Associate
1 month ago
Stanford University is seeking a highly motivated and detail-oriented Clinical Research Coordinator Associate to join our team. As a Clinical Research Coordinator Associate, you will play a critical role in the coordination and management of clinical studies, ensuring the highest level of quality and compliance with regulatory requirements.
Key Responsibilities- Coordinate and manage clinical studies from startup to close-out, ensuring timely completion and compliance with regulatory requirements.
- Recruit and screen study participants, obtain informed consent, and manage participant data.
- Collect and manage study specimens and process data for clinical research projects.
- Ensure compliance with research protocols, review and audit case report forms, and prepare regulatory submissions.
- Assemble study kits, monitor scheduling of procedures, and coordinate documents.
- Monitor expenditures and adherence to study budgets, and resolve billing issues.
- Interact with principal investigators, ensuring patient safety and adherence to proper study conduct.
- Ensure essential documentation and recording of patient and research data in appropriate files.
- Bachelor's degree in a related field or an equivalent combination of education and experience.
- Strong interpersonal skills, proficiency with Microsoft Office, and knowledge of medical terminology.
- Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Occasional evening and weekend hours may be required.
Stanford University is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.