Clinical Research Coordinator - Clinical Research
CenExel
Summary
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Job description
Essential Responsibilities and Duties
- Assists with coordinating all aspects of patient involvement from study initiation until study completion.
- Organizes research information for clinical trials.
- Observes subjects and assists with data analysis and reporting.
- Schedules the collection of data.
- Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
- Reports research data to maintain quality and compliance.
- Performs administrative and regulatory duties related to the study as appropriate.
- Participates in other protocol development activities.
- Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
- Educates potential participants and caregivers on protocol specific details and expectations.
- Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
- Assumes other duties and responsibilities as assigned.
Education/Experience/Skills
- High school graduate or equivalent; Bachelor's Degree, preferred.
- 1+ years of experience as a Clinical Research Coordinator (Required)
- Phlebotomy Experience (Highly Desired)
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
- Strong leadership and mentorship skills.
- Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
- Crisis management and problem-solving skills; ability to react calmly and effectively in emergent situations.
- Works independently as well as functioning as part of a team.
- Must be able to effectively communicate verbally and in writing.
Working Conditions
- Indoor, Office environment.
- Shift work, depending on location.
- Essential physical requirements include sitting, typing, standing, and walking.
- Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
- Reporting to work, as scheduled, is essential.
- Overnight travel may be required for training and/or investigative meetings.
Requirements
- High school graduate or equivalent
- 1+ years of experience as a Clinical Research Coordinator
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
- Strong leadership and mentorship skills
- Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level
- Crisis management and problem-solving skills; ability to react calmly and effectively in emergent situations
- Works independently as well as functioning as part of a team
- Must be able to effectively communicate verbally and in writing
Benefits
- Health Insurance
- Dental
- Vision
- LTD
- STD
- Life Insurance
- 401k
Company overview
CenExel is a leading integrated clinical research site network operating across major metropolitan areas throughout the United States. Founded in 2018 and headquartered in Salt Lake City, Utah, the company operates 18 Centers of Excellence that collectively represent over 40 years of clinical research experience. CenExel specializes in providing comprehensive clinical trial services to pharmaceutical companies, biotechnology firms, and clinical research organizations, with particular expertise in central nervous system (CNS) disorders and early-phase clinical research. The company's nationwide network delivers deep scientific expertise, premium data quality, operational efficiencies, and exceptional patient engagement to drive successful clinical trial outcomes. With more than 1,200 employees across its network, CenExel focuses on accelerating the development of life-changing therapies through its patient-centered approach and commitment to research excellence. The company serves as a strategic partner for sponsors seeking to optimize clinical trial performance, from site selection through study close-out, while maintaining rigorous standards for patient care and scientific integrity.