Clinical Research Coordinator Jobs at CTI, USA | Life Science Candidates, Apply Now
A rare chance has emerged for professionals in the life sciences sector as CTI seeks to fill clinical research coordinator jobs in Cincinnati, Ohio. This full-time position offers a unique opportunity to coordinate clinical research studies while adhering to Good Clinical Practices and regulatory standards.
- Job Position: Clinical Research Coordinator (level dependent on experience)
- Job Category: Clinical Research Center
- Requisition Number: CLINI001988
About The Company
CTI is a leading clinical research organization dedicated to advancing medical science through innovative research. Operating in the life sciences space, CTI focuses on conducting Phase I through Phase IV clinical studies to bring life-changing therapies to market. With a commitment to quality and compliance, CTI is recognized for its exceptional culture and support for employee development.
Clinical Research Coordinator Jobs: Job Description
The Clinical Research Coordinator will coordinate the conduct of clinical research studies in accordance with Good Clinical Practices (GCPs), International Harmonization Guidelines, and Standard Operating Procedures (SOPs). In these clinical research coordinator jobs, the role involves managing studies from pre-study planning through to successful completion of all study visits.
Clinical Research Coordinator Jobs – Key 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 and collaborate with the Recruitment Department in 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 staff as needed.
- Ensure consistency and effective communication during study visits, maintaining subject safety and assessing feedback from study participants.
- Coordinate and conduct study visits, ensuring compliance with clinical protocols and applicable regulations.
- Interact with investigators or study sponsors to ensure appropriate medical evaluation and care for study participants.
- Facilitate sponsor monitoring and database clean-up processes through interaction with the sponsor Clinical Research Associate.
- Attend sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.
Eligibility Criteria Required For Clinical Research Coordinator Jobs
- 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.
- Clinical Research Coordinator Certification (CCRC) is preferred.
- Associate or Bachelor’s Degree in Nursing is preferred.
- Advanced Cardiac Life Support (ACLS) is preferred.
Why CTI?
- Advance Your Career – CTI supports career progression through structured mentoring programs and leadership courses, along with ongoing education and training opportunities.
- Join an Award-Winning Team – CTI boasts a unique culture recognized across 60 countries, promoting work-life balance and generous health benefits.
- Make a Lasting Impact – The organization focuses on developing treatments for critically ill patients, making a significant difference in their lives.
CTI’s clinical research coordinator jobs offer a remarkable opportunity for qualified candidates to contribute to the advancement of medical science. With a focus on life sciences jobs in Ohio, CTI encourages interested individuals to apply at the earliest. This is an excellent chance to be part of a team that is dedicated to making a lasting impact in the field of clinical research.
