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Clinical Research Associate Position
1 week ago
Job Overview
We are seeking a highly skilled Clinical Research Associate to join our team. As a leader in medical science, we are committed to solving the challenges that matter most.
Key Responsibilities
- Source Verification: Conduct thorough comparisons of data recorded on Case Report Forms against source documents, ensuring accuracy and completeness.
- Communications: Maintain clear written communication with clinical sites and project team members through monitoring reports, follow-up letters, study memos, and general correspondence.
- Training: Ensure all site personnel are adequately trained and prepared to conduct the clinical study in accordance with protocol and applicable regulations.
- Site Compliance: Identify and address any non-compliance issues, clearly documenting and escalating as required.
- Event Reporting: Ensure timely identification, documentation, and reporting of all reportable events per protocol and applicable requirements.
- Collaboration: Participate in study-specific meetings, teleconferences, and trainings, collaborating with cross-functional team members and study sites throughout all study phases.
- Documentation: Manage study contracts, request/collection of relevant investigator/site documentation, review, and approve documents in applicable databases.
