The Clinical Research Coordinator manages day-to-day clinical trial operations, overseeing participant recruitment, screening, and informed consent to ensure safety and compliance. The role maintains study documentation, coordinates site visits, collects data, and collaborates with investigators and sponsors while preparing for audits. Candidates require a Bachelor's degree in a life sciences or related field along with 1 to 3 years of clinical research coordination experience and knowledge of Good Clinical Practice guidelines.
RDI is looking for a proactive and organized Clinical Research Coordinator (CRC) to join our talented team. In this role, you will play a pivotal part in managing clinical trials, ensuring they adhere to regulatory requirements and the highest ethical standards. As a CRC at RDI, you will oversee the day-to-day operations of clinical studies, acting as the main point of contact between study participants, investigators, and our internal research teams. You will be responsible for participant recruitment, screening, and ensuring informed consent is obtained to facilitate patient safety and compliance. You will also manage data collection, assist our research team with protocol implementation, and ensure that trials are conducted smoothly from start to finish. If you are passionate about clinical research and want to contribute to groundbreaking studies that can change lives, this opportunity at RDI is for you.
Key Responsibilities
- Recruit and screen study participants and ensure their eligibility in accordance with the study protocol.
- Facilitate the informed consent process, ensuring that participants understand the study requirements.
- Coordinate and conduct site visits, including data collection and monitoring for compliance with the study protocol.
- Maintain accurate and complete study documentation, including source documents and regulatory files.
- Collaborate with Principal Investigators and study sponsors, providing updates and addressing any issues that may arise.
- Prepare for audits and inspections by ensuring all study records are up to date and in compliance.
- Assist with the management of study budgets and timelines.
Requirements
- Bachelor's degree in life sciences, nursing, or a related field; relevant certifications (e.g., CRC, CCRA) are a plus.
- 1-3 years of experience in clinical research coordination or a related role.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory standards.
- Excellent organization and time management skills, with the ability to handle multiple studies simultaneously.
- Strong written and verbal communication skills, with the ability to engage with participants and stakeholders effectively.
- Proficient in using electronic data capture systems and clinical trial management software.
- Ability to work independently and collaboratively in a fast-paced research environment.
Benefits
- Health Care Plan (Medical, Dental & Vision)
- Retirement Plan (401k, IRA)
- Life Insurance (Basic, Voluntary & AD&D)
- Paid Time Off (Vacation, Sick & Public Holidays)
- Long-term growth through the RDI Operator Studio
- Everyone who joins RDI has the opportunity to participate in the RDI Operator Studio as part of their long-term growth here. Through hands-on work, coaching, and review of real study problems, you can deepen your expertise, learn how the whole business works, and earn broader responsibility as your judgment develops. You enter through this role; your growth does not have to stop at its original scope.
- Read our CEO’s open letter to understand how we work and what becoming an RDI operator means. Watch videos from our CEO and team to learn more about the people and work behind it.
- Read the open letter
- Watch the CEO and team videos
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