Clinical Trials Coordinator – Impactful CNS Research

CenExel Clinical Research; Salt Lake City (UT); Vor Ort; USD 30.000 - 33.000; Vollzeit

Benefits dieser Stelle

Health Insurance

Dental

Vision

LTD/STD/Life Insurance

401k

Zusammenfassung

CenExel Clinical Research in Salt Lake City is seeking a Clinical Research Coordinator I to coordinate all aspects of trials in line with ICH, GCP, and protocol guidelines. The role involves data collection, safety assessments, and ongoing collaboration with sponsors and vendors.

Shift is 6a-6p, days vary by study needs; compensation ranges $22-24 per hour, commensurate with experience and education. Full-time position offering comprehensive benefits after 30 days of employment.

Qualifikationen

• Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position.
• CCRC certification preferred.
• 2-3 years of experience in the medical field, preferred.
• 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.

Aufgaben

• Coordinate all aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
• Organize research information for clinical trials.
• Observe subjects and assist with data analysis and reporting.
• Schedule 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.

Kenntnisse

Clinical research coordination

Regulatory knowledge

Communication skills

Team leadership

Problem solving

Independent work

Ausbildung

CCRC certification

Jobbeschreibung

CenExel Clinical Research in Salt Lake City is seeking a Clinical Research Coordinator I to coordinate all aspects of trials in line with ICH, GCP, and protocol guidelines. The role involves data collection, safety assessments, and ongoing collaboration with sponsors and vendors.

Shift is 6a-6p, days vary by study needs; compensation ranges $22-24 per hour, commensurate with experience and education. Full-time position offering comprehensive benefits after 30 days of employment.