Clinical Research Program Manager, Seidman Cancer Center (Hybrid)

University HospitalsCleveland, OH
Hybrid

About The Position

In collaboration with the SCC CTU director, this role provides leadership for the clinical research program for the UH SCC Clinical Trials Unit. The position oversees the organization of research operations, ensuring proper resource allocation and adherence to protocol requirements. It also assists the Director, Clinical Trials with departmental activities to maximize efficiency of management control systems, programs, policies, work methods, and procedures. The Clinical Research Program Manager manages clinical trial processes, ensuring compliance with internal SOPs, GCP guidelines, sponsor guidelines, and applicable regulatory regulations. Additionally, this role oversees and implements program-wide projects and provides training for clinical team members.

Requirements

  • Bachelor's Degree (Required)
  • 5+ years of clinical research experience which includes at least 3 years demonstrated management, supervisory or project management experience
  • Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively.
  • Strong leadership skills to train and supervise direct reports with effective experience in resource planning.
  • Ability to work consistently and effectively as part of a high performance work team.
  • Good judgment, initiative and problem solving skills.
  • Excellent written communication skills and interpersonal and verbal communication skills.
  • Ability to follow through and consistently demonstrate primary job responsibilities are current.
  • Knowledge of computer operations and demonstrated computer skills in a variety of software environments (ie Excel, Access, Word, database applications).

Nice To Haves

  • Master's Degree (Preferred)
  • Research certification (i.e., SoCRA, ACRP) (Preferred)

Responsibilities

  • Provide leadership for the clinical research program for the UH SCC Clinical Trials Unit in collaboration with the SCC CTU director.
  • Oversee the organization of research operations with the proper allocation of resources and adherence to protocol requirements.
  • Assist the Director, Clinical Trials in regard to specific departmental activities with the goal of maximizing efficiency of management control systems, programs, policies, work methods and procedures.
  • Manage the clinical trial processes and ensure that clinical trials are generated, documented and reported in compliance with internal SOPs, GCP guidelines, sponsor guidelines and current applicable regulatory regulations.
  • Oversee and implement program wide projects and provide training efforts for the clinical team member(s).
  • Performs other duties as assigned.
  • Complies with all policies and standards.
  • Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients.
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