What are the responsibilities and job description for the Clinical Research Coordinator position at Paradigm Clinical Research?
Company Description
Paradigm Clinical Research is a well-established and professionally managed clinical research organization operating wholly owned sites. Our mission is to advance the human condition through high-quality clinical trials that provide access to diverse and under-represented patient populations and investigators. We are dedicated to lowering barriers to participation in clinical studies and delivering exceptional value to our client sponsors. Recognized as an employer of choice, we foster professional growth, offer a leading benefits package, and promote a supportive and collaborative work culture.
Role Description
This full-time on-site role is located in Wheat Ridge, CO. The Clinical Research Coordinator will manage day-to-day operations for clinical trials, including obtaining informed consent from participants, adhering to study protocols, and ensuring compliance with regulations. Additional duties include coordinating patient recruitment, maintaining accurate documentation, preparing study materials, and collaborating with clinical teams to execute trials efficiently.
Qualifications
- Proficiency in obtaining and documenting informed consent from study participants
- Experience implementing and following clinical research protocols
- Strong background in clinical research, including trial coordination and study execution
- Knowledge of clinical trials and their regulatory requirements
- Excellent organizational, communication, and interpersonal skills
- Ability to work effectively in an on-site, team-based environment
- Proficient in data collection and management tools
- Bachelor’s degree in a related field or equivalent work experience in clinical research