Academic Center Project Manager I - Clinical Events Committee HVTI

                    

At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day.

                        

We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One.

                                    

Job Title

Academic Center Project Manager I - Clinical Events Committee HVTI

                        

Location

Cleveland

                    

Facility

Cleveland Clinic Main Campus

                     

Department

HVTI Research and Registries-Main Campus Hospital

                      

Job Code

T98809

                     

Shift

Days

                       

Schedule

8:00am-4:30pm

                       

Job Summary

                         

Job Details

Join the Cleveland Clinic team where you will work alongside passionate caregivers and make a lasting, meaningful impact on patient care. Here, you will receive endless support and appreciation while building a rewarding career with one of the most respected healthcare organizations in the world.      

 

The Project Manager role participates in project management functions for single and multi-institutional research trials, including Phase I–IV clinical studies. You will coordinate and manage day-to-day organizational and operational aspects of trial conduct. This role provides central leadership by facilitating key communications across stakeholders, contributing clinical insight into trial design and implementation, and driving initiatives that ensure high-quality study conduct and performance. In this role you will collaborate with outside organizations, sponsors, CROs, physicians, internal staff, and C5 caregivers, while learning the full research lifecycle. Although not patient-facing, they play a critical role by collecting and reviewing source documents to determine whether clinical events occurred, then coordinating adjudication with study partners. 

 
A caregiver in this position works 8:00am—4:30pm. Travel will be required! 

 
A caregiver who excels in this role will:  

• Collaborate with physicians, sponsors, and research teams to facilitate study planning, protocol development, and overall project execution in alignment with Cleveland Clinic standards. 

• Analyze site strengths and weaknesses as they relate to the intended protocol and selection of qualified investigators/sites. 

• Perform ongoing assessment of investigator/site performance. 

• Develop or contribute to the performance standards to ensure the integrity of the study, quality of study conduct and study performance. 

• Spearhead initiatives to improve quality and makes recommendations to discontinue site if necessary. 

• Maintain professional relationships with sponsors, which includes frequent, open communication and associated documentation. 

• Prepare and review study status reports. 

• Act as a liaison between the Cleveland Clinic sites, sponsors, CRO or other vendors and the FDA. 

• Act as the primary point of contact for the academic leadership committees and coordinate their activity including charter development to ensure successful conduct of the trial. 

• Contribute to planned site communication and training (i.e., Investigator meetings, newsletters, study progress updates, telephone communication, supportive reinforcement of sponsor communication, etc.) 

• Initiate and develop educational initiatives and