Clinical Research Coordinator (level dependent on experience)

CTI Clinical Trial and Consulting Services • Norwood, OH

38d • Hybrid

About The Position

Coordinate the conduct of
Phase I through Phase IV clinical research studies in
accordance with Good Clinical Practices (GCPs), International Harmonization
Guideline and Standard Operating Procedures (SOPs) beginning with pre-study
planning through successful completion of all study visits.

Requirements

• 1+ year of experience as a clinical research coordinator or in a similar position within the medical or mental health field
• Bachelor’s degree in life sciences or equivalent combination of related experience and education in the medical or mental health field

Nice To Haves

• Clinical Research Coordinator Certification (CCRC) is preferred
• Associate or Bachelor’s Degree in Nursing is preferred
• Advanced Cardiac Life Support (ACLS) is preferred

Responsibilities

• Maintain a good level of knowledge and understanding of assigned protocols, including all protocol requirements for study visits, obtaining informed consent, study visit schedules, tests, procedures, laboratory information, and drug accountability requirements
• Recruit subject volunteers for studies; Work with the Recruitment Department with developing study-related materials and interview questionnaires
• Create source templates for study documentation, complete case report forms, and other study specific documents seeking assistance from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed
• Ensure consistency and effective communication during study visits and assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used
• Coordinate and conduct study visits; Assure all procedures are conducted in compliance with the clinical protocol and in accordance with all applicable regulations and in compliance with GCPs
• Interact with Investigators or study sponsors as needed to assure the study participant receives appropriate medical evaluation and care when needed
• Interact with the sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process
• Attend sponsor Investigator/Study Coordinator meetings as needed for assigned protocols
• Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader, or Clinical Site Director, as needed
• Actively seeks out development opportunities
• Behave cooperatively and constructively; Follow all company policies, state, local, federal, and other applicable laws and guidelines; Comply with all job-specific requirements

Benefits

• Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
• Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 501-1,000 employees