Clinical Research Coordinator

Responsibilities

• Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies 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
• Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately
• Monitors, and 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)
• Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes
• Assists the CTM in planning, creating processes, trainings and development of staff
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive

Preferred

• Bachelors Degree, preferred
• CCRC certification preferred
• 2-3 years of experience in the medical field, preferred

Benefits

• Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k for full time employees after 30 days of employment
• An exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance
• CenExel is a clinical research site network supporting phase I-IV clinical trials. It is a sub-organization of Webster Equity Partners.
• Salt Lake City, Utah, USA
• http://www.CenExelresearch.com
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Engineering and Development
• Trends of Total Sponsorships
• *2026
• (1)
• 2023
• 2020
• Late Stage
• Total Funding
• unknown
• 2025-04-12
• Acquired
• 2023-04-01
• Private Equity
• Leadership Team
• Sybrand Pretorius
• Chief Executive Officer (CEO)
• Recent News
• PR Newswire
• CenExel Appoints Bethany Sensenig as Chief Financial Officer
• 2026-06-18
• CenExel Pain Task Force Innovates Research Approach for Next Generation, Non-Opioid Pain Therapies
• 2026-06-11

Qualifications

• Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position
• High school graduate or equivalent
• 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
• Bachelors Degree, preferred
• CCRC certification preferred
• 2-3 years of experience in the medical field, preferred

Required skills

• CCRC Certification, Clinical Trial Regulations, Federal Regulations for Human Subjects Research, Leadership and Mentorship

Preferred skills

• 2-3 years of experience in the medical field, preferred, Bachelors Degree, preferred, CCRC certification preferred

Experience

• 2-3 years