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Clinical Oversight Manager Jobs (NOW HIRING)

Mallinckrodt

Oversight Manager

Malvern, PA · On-site

$130K - $150K/yr

Job Title Oversight Manager Requisition JR000015795 Oversight Manager (Open) Location Malvern, PA ... In collaboration with Clinical Operations, this role supports the identification of sites for ...

Therakos

Oversight Manager

Malvern, PA · Remote

$130K - $150K/yr

Job Title Oversight Manager Requisition JR000015795 Oversight Manager (Open) Location Malvern, PA ... In collaboration with Clinical Operations, this role supports the identification of sites for ...

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How much do clinical oversight manager jobs pay per year?

As of May 28, 2026, the average yearly pay for clinical oversight manager in the United States is $79,349.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $88,500.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Oversight Manager vs Clinical Program Coordinator?

AspectClinical Oversight ManagerClinical Program Coordinator
Required CredentialsTypically requires a nursing degree, clinical certification, or advanced healthcare qualificationUsually requires a bachelor's degree in health sciences or related field
Work EnvironmentOversees clinical operations, manages staff, ensures compliance in healthcare settingsCoordinates clinical activities, manages schedules, and supports program implementation
Employer & Industry UsageHospitals, clinics, healthcare organizationsResearch institutions, healthcare providers, clinical trial sites

The Clinical Oversight Manager focuses on supervising clinical staff and ensuring compliance with healthcare standards, while the Clinical Program Coordinator handles the day-to-day coordination of clinical activities. Both roles are essential in healthcare settings but differ in scope and responsibilities.

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What cities are hiring for Clinical Oversight Manager jobs? Cities with the most Clinical Oversight Manager job openings:
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Clinical Oversight Manager jobs near you
Infographic showing various Clinical Oversight Manager job openings in the United States as of May 2026, with employment types broken down into 3% As Needed, 73% Full Time, 17% Part Time, 1% Temporary, and 6% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $79,349 per year, or $38.1 per hour.

Senior Clinical Oversight Manager

Kailera Therapeutics, Inc.

Waltham, MA • On-site

Other

Posted 9 days ago

Job description

What You'll Do:

The Senior Clinical Oversight Manager (COM) is responsible for executing the Clinical Monitoring Oversight visit process and Clinical Oversight Metrics. The Senior COM represents Kailera during Clinical Oversight visits and oversees study execution to ensure compliance with ICH GCP, and applicable regulations. The Senior COM is involved in planning, execution, and delivery of oversight processes including Standard Operating Procedures (SOP) and work instructions. 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Develops the Clinical Monitoring Oversight strategy across studies, including development and oversight of Clinical Monitoring Oversight SOPs and templates, Clinical Oversight Monitoring plans, managing Monitoring Oversight Service Provider (SP) activities, providing study/program/SP level reporting, and leading monthly TMF health checks
  • Evaluates and provides recommendations to the study team on Oversight Service Provider activities to ensure the appropriate scope of work, oversight, and training of clinical oversight CRAs to achieve study milestones within agreed upon timelines, budget and quality
  • Assigns oversight visits at trial sites based on strategic criteria to evaluate compliance of trials with local regulatory requirements; overall data quality and integrity; and human subject protection
  • Provides oversight on service provider execution of clinical trial activities in accordance with Kailera SOPs, ICH Guidelines, and Good Clinical Practice (GCP)
  • Develops key performance indicators (KPIs) and evaluates service provider operational data against KPIs to identify potential performance gaps
  • Collaborates with the Clinical Oversight team, Clinical Quality Management, and Clinical Study Team to implement corrective actions and monitor progress through resolution
  • Facilitate resolution of region specific and site management related challenges
  • Acts on behalf of Business Operations on cross-functional project teams; interacts with internal and external groups
  • Assist with creation and delivery of department initiatives, improvement plans, and/or training
  • Selects and oversees Oversight CRAs globally, driving the team to ensure study deliverables are met with efficiency and quality in accordance with applicable SOPs, regulations, GCP, Key Performance Indicators (KPIs), and study-specific requirements
  • Responsible for ensuring Oversight CRAs maintain their sites/studies as inspection ready, including the TMF, for health authority inspections
  • Conduct periodic quality visits for Oversight CRAs, as needed
  • Ensure the oversight CRAs are reviewing and ensuring data integrity, accuracy, and completeness at the clinical study sites
  • Support and liaise with clinical site personnel, as needed
  • Review contracts and approve vendor invoices

Qualifications:

  • Minimum of 8+ years of clinical trial experience with strong knowledge of the clinical development process
  • Experience with Phase I-III clinical trials, risk-based monitoring, and CRA Management
  • Proficient in oversight tools and systems (CTMS, eTMF, dashboards, Microsoft Office)
  • Experience with Vendor oversight, KPI tracking, and issue management
  • Strong leadership, collaboration, and communication skills with the ability to manage and motivate team members (e.g., internal staff and external investigators/consultants)
  • Excellent organizational, analytical, and interpersonal skills; able to work independently and in teams
  • In-depth knowledge of ICH-GCP, FDA, EMA, and global regulatory requirements
  • Ability to manage complexity in a fast-paced environment
  • Must have strong clinical study management, communication (oral and written), and analytical skills
  • Must be able to travel

Education:

  • Bachelor's degree in a scientific or healthcare-related field

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