Clinical Research Associate
1 week ago
Toku develops tools using AI and retinal photography to enable accessible healthcare for early and accurate diagnosis of health conditions.
Who You Are:
Toku Inc. is seeking a dedicated and detail-oriented Clinical Research Associate to help our dynamic team in the fast-paced world of clinical trials. The ideal candidate will possess extensive clinical research experience and will be responsible for monitoring clinical trials, ensuring compliance with regulatory standards, and contributing to the development and testing of new medical devices.
What You'll Do:
Key Responsibilities:
- Document and report on clinical trial progress, including site visits, trial status, and participant safety.
- Communicate effectively with site staff, investigators, and other stakeholders to ensure trial objectives are met.
- Work closely with Contract Research Organizations to monitor the conduct of clinical trials, ensuring compliance with the protocol, overall clinical objectives, and applicable regulatory requirements.
- Review and verify data collected during clinical trials to ensure accuracy and integrity.
- Manage documents required for the proper conduct of a clinical trial, including consent forms, case report forms, and other documentation.
- Assist in the preparation and review of trial-related documents, such as protocols, investigator brochures, and summary reports.
- Participate in the development and implementation of recruitment strategies to increase patient enrollment.
- Provide training and support to site staff to ensure compliance with study protocols and all applicable procedures and regulations.
- Address and resolve any issues that may arise during the trial, escalating complex issues to senior staff as necessary.
- Stay informed of industry trends, new regulations, and best practices in clinical research to enhance job performance and trial success.
- Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
- Minimum of [X] years of experience in clinical research, preferably as a Clinical Research Associate or Clinical Research Coordinator or similar role.
- Strong understanding of GCP (Good Clinical Practice) and regulatory compliance guidelines for clinical trials.
- Excellent organizational skills with the ability to manage multiple responsibilities in a fast-paced environment.
- Strong communication and interpersonal skills, with the ability to work effectively both independently and as part of a team.
- Proficient in the use of clinical trial management software and Microsoft Office Suite.
What We Offer:
Salary range: $120k-$150k
Remote Work
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