Clinical Trials Program Manager

ccf; Town of Weston (WI); On-site; USD 90,000 - 120,000; Full time

Job summary

Cleveland Clinic Health System in Weston seeks a Clinical Research Project Manager to oversee administrative functions for multi-institutional trials. You will coordinate daily trial activities, manage communications among sponsors, sites, and IRBs, and provide clinical perspective on study design and conduct.

The role requires a Bachelor’s degree in a health care discipline or related field, experience in clinical research, and familiarity with FDA regulations and GCPs.

Qualifications

• Bachelor's degree or higher in a healthcare, science, or related field is required.
• SOCRA or ACRP certification desirable.
• Experience with FDA regulations, GCPs and internal SOPs.

Responsibilities

• Oversees administrative functions of single/multi-institution trials.
• Coordinates daily organization and operational activities for trials (Phase I-IV).
• Facilitates trial communications and provides clinical perspective on design and conduct.
• Manages a trials team and coordinates budgets, contracts, and regulatory docs.
• Maintains relationships with sponsor, IRBs, FDA, and sites.
• Coordinates development and approval of protocols andCRFs.

Skills

Clinical research

Project management

Communication skills

Regulatory knowledge

Cross-functional coordination

Education

Bachelor's degree in nursing, general science, a health care discipline, or computer science with programming emphasis

Associate's degree substitute for work experience

Master’s degree substitute for work experience

HS Diploma/GED substitute for work experience

Job description

Cleveland Clinic Health System in Weston seeks a Clinical Research Project Manager to oversee administrative functions for multi-institutional trials. You will coordinate daily trial activities, manage communications among sponsors, sites, and IRBs, and provide clinical perspective on study design and conduct.

The role requires a Bachelor’s degree in a health care discipline or related field, experience in clinical research, and familiarity with FDA regulations and GCPs.