Manager, Global Clinical Monitoring

Precision Medicine Group

Manager Global Clinical Monitoring leading team of CRAs at Precision Medicine Group. Focusing on quality operations and career development in clinical research.

Posted 5/7/2026full-timeRemote • 🇺🇸 United StatesSeniorLead💰 $121,800 - $182,600 per yearWebsite

About the role

Key responsibilities & impact

The Manager Global Clinical Monitoring (GCM) offers an additional development path for clinical research professionals. Responsibilities are focused on the management and career development of the organization’s Clinical Research Associate (CRA) workforce as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations.
This position requires the ability to independently lead, manage, and motivate a team of CRAs (employee and/or consultant) to a standard consistent with Precision for Medicine’s values and overall focus on quality.
Generate action plans and provide developmental/strategic oversight to optimize CRA services, with a focus on high quality delivery of individual/team/departmental goals.
Assist with and contribute to project resourcing to ensure proper level and allocation resource is assigned for each project within their hierarchy (with respect to project phase). Update tracking systems and interface with project teams.
Collaborate with the Clinical Team Leads/Clinical Trial Managers and Clinical Operations Management Team to ensure that resource needs and site requirements are met appropriately.
Develop, mentor, manage and coach CRA staff to progress their skills so that Precision for Medicine quality standards are maintained. Advocate individual career development, and individual responsibility/accountability.
Identify quality risks and issues and recommend corrective action plans as needed to leadership team to address deficiencies in performance of employees.

Requirements

What you’ll need

Graduate, postgraduate, 4-year college degree, or equivalent experience ideally in a scientific or healthcare discipline
At least 7 years or more in clinical operations, data management or related discipline either in CRO or Pharmaceutical industry with a minimum of 5 years onsite monitoring experience.
Monitoring experience includes use of electronic data capture systems as well as paper and electronic medical records.
3-5 years of direct supervisory experience managing CRAs is expected in candidates for this position.
Ability to drive and availability for domestic and international travel including overnight stays, with an expectation of travel approximately 25%.

Benefits

Comp & perks

Health insurance
401(k) matching
Discretionary annual bonus
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation

ATS Keywords

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Hard Skills & Tools

clinical operationsdata managementelectronic data capture systemsmedical records managementproject resourcingquality risk managementaction plan developmentteam managementsupervisory experiencecareer development

Soft Skills

leadershipmotivationcollaborationcoachingmentoringcommunicationstrategic oversightproblem-solvingaccountabilityadvocacy