Clinical Research Program Manager

University Hospitals

. Provide leadership for the UH Seidman Cancer Center Clinical Trials Unit clinical research program in collaboration with the SCC CTU director .

Posted 9/18/2026full-timeCleveland • Ohio • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical research management, including oversight of clinical trial processes, adherence to GCP guidelines, and effective resource allocation. Strong leadership and communication skills are essential for training team members and ensuring compliance with organizational policies.

Highest-signal resume keywords

Clinical Research ManagementGCP Guidelines ComplianceLeadership SkillsProject Management ExperienceResearch Certification (SoCRA or ACRP)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesProtocol RequirementsResource AllocationData ManagementProblem-Solving Skills

Soft Skills

Detail-OrientedTime ManagementInterpersonal CommunicationInitiative

Tools & Technologies

ExcelAccessWordDatabase Applications

Certifications & Qualifications

SoCRA CertificationACRP Certification

Industry Keywords

Clinical TrialsProtected Health Information (PHI)SOPsHigh-Performance Work Team

About the role

Key responsibilities & impact

Provide leadership for the UH Seidman Cancer Center Clinical Trials Unit clinical research program in collaboration with the SCC CTU director
Oversee research operations, resource allocation, and adherence to protocol requirements
Assist the Director, Clinical Trials with departmental activities to maximize efficiency of management control systems, programs, policies, work methods, and procedures
Manage clinical trial processes and ensure trials are generated, documented, and reported in compliance with internal SOPs, GCP guidelines, sponsor guidelines, and applicable regulations
Oversee and implement program-wide projects
Provide training for clinical team members
Perform other duties as assigned
Comply with organizational policies and standards
Maintain patient Protected Health Information (PHI) safely and securely

Requirements

What you’ll need

Bachelor's Degree (Required)
5+ years of clinical research experience, including at least 3 years of demonstrated management, supervisory, or project management experience (Required)
Detail-oriented, able to work independently on multiple tasks and manage time effectively
Strong leadership skills to train and supervise direct reports, with effective resource-planning experience
Ability to work consistently and effectively as part of a high-performance work team
Good judgment, initiative, and problem-solving skills
Excellent written, interpersonal, and verbal communication skills
Ability to follow through and consistently demonstrate that primary job responsibilities are current
Knowledge of computer operations and demonstrated computer skills in software environments including Excel, Access, Word, and database applications
Research certification such as SoCRA or ACRP (Preferred)
Ability to safely and securely maintain Protected Health Information (PHI) and comply with applicable policies and requirements
Ability to travel approximately 10%

Benefits

Comp & perks

Full-time regular employment
Hybrid work arrangement
Day shift
Annual training
UH Code of Conduct and workplace policies and procedures
Research certification support/preference (SoCRA, ACRP listed as preferred)