We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This part-time position offers an exciting opportunity to work within a dynamic environment, impacting the landscape of clinical research. As part of a small but impactful organization, you will play a crucial role in the execution and management of clinical trials, contributing to groundbreaking advancements in the life sciences sector.

Key Responsibilities:

Assist in the planning and coordination of clinical trial protocols and study procedures.
Recruit and screen potential study participants while ensuring compliance with regulatory guidelines.
Monitor clinical trial activities to ensure adherence to timelines, budgets, and quality standards.
Collect, manage, and maintain accurate clinical data, and ensure proper documentation is completed.
Facilitate communication between clinical trial stakeholders, including investigators, sponsors, and participants.
Conduct regular training sessions for staff on clinical trial regulations and study requirements.
Compile reports on progress, issues, and outcomes of clinical trials for stakeholders and regulatory agencies.

Qualifications:

Demonstrated experience in managing clinical trials.
Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
Proficiency with clinical databases and software tools.