Clinical Research Coordinator - Clinical Research

Responsibilities

• 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. 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

• Bachelor's Degree

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
• Late Stage
• Total Funding
• unknown
• 2025-04-12
• Acquired
• 2023-04-01
• Private Equity
• Leadership Team
• Sybrand Pretorius
• Chief Executive Officer (CEO)
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Qualifications

• 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
• Bachelor's Degree

Required skills

• Clinical Research Coordination, Clinical Trial Regulations, Federal Regulations for Human-Subjects Research

Preferred skills

• Bachelor's Degree

Experience

• 1+ years