Job Overview:
The Clinical Research Associate Leader is a key professional in the clinical trial process, responsible for overseeing site management and monitoring tasks. This role is part of a larger team that ensures the successful execution of clinical trials.
Key Responsibilities:
* Coordinate site identification, feasibility assessment, and selection to ensure the right sites are involved in the trial.
* Monitor trial activities, ensuring compliance with regulatory requirements and standard operating procedures (SOPs).
* Collaborate with investigators to motivate and train them on protocol, investigational product, and trial requirements.
* Manage trial sites, including data verification, audits, and issue resolution, to ensure data integrity.
* Perform translation verification and site close-out visits to confirm completion of trial activities.
* Mentor junior staff members and perform additional responsibilities as assigned.
Required Skills and Qualifications:
To be successful in this role, you should have a degree in pharmacy, medical, nursing, biological science, or other health-related disciplines, preferably with 5 years of experience in clinical trial monitoring and/or site management.
About You:
We're looking for individuals who possess strong communication, organizational, and leadership skills. If you're passionate about delivering high-quality results and contributing to the success of clinical trials, we encourage you to apply.