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Clinical Program Manager

  • Clinical Program Manager job type Posted on: Nov 01, 2026
  • Clinical Program Manager experience level TCWGlobal
  • Clinical Program Manager employment type San Diego, California
  • Clinical Program Manager salary Salary: $41 per hour
  • Clinical Program Manager employment type Onsite
  • Clinical Program Manager salary Full-time

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Job Title :

Clinical Program Manager

Job Type :

Full-Time

Job Location :

San Diego California United States

Remote :

No

Jobcon Logo Job Description :

Clinical Program ManagerPay Rate: $41.92–$54.48/hourDuration: 12-Month AssignmentHours: Full-Time, 40 hours per weekLocation: San Diego, CASummaryWe are seeking a Clinical Program Management professional to support clinical operations activities, study deliverables, documentation, data review, and cross-functional coordination.In this role, you will partner with clinical teams, vendors, sites, and internal stakeholders to help maintain accurate, timely, and compliant clinical work. The ideal candidate has experience supporting clinical processes, study coordination, documentation, and operational activities within established quality and regulatory expectations.What You'll DoSupport the planning, coordination, and execution of clinical activities and deliverablesMaintain study-related records, trackers, timelines, meeting materials, and documentation in accordance with established processesCoordinate information, communications, and follow-up with clinical teams, vendors, sites, and internal stakeholdersReview study documents, data, reports, and operational materials for accuracy, completeness, and consistencyTrack issues, action items, risks, and potential delays, and communicate relevant updates to appropriate stakeholdersSupport process updates, training coordination, and documentation needed to maintain clinical readinessParticipate in cross-functional clinical meetings and contribute to status updates and follow-up activitiesContribute to continuous improvement initiatives and efforts to strengthen clinical processesWhat You BringBachelor's degree in a related scientific, healthcare, business, or technical field, or equivalent education and experienceTypically 2+ years of relevant experience supporting functional projects, processes, analysis, documentation, or operationsKnowledge of clinical processes, documentation practices, and study coordinationFamiliarity with applicable quality or regulatory expectationsAbility to manage timelines, records, data, and stakeholder follow-up with accuracy and attention to detailStrong organizational skills and ability to follow established proceduresSound judgment and attention to detailStrong written and verbal communication skillsAbility to collaborate effectively across teams and functionsTCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Jobcon Logo Position Details

Posted:

Nov 01, 2026

Reference Number:

10440_4472578598

Employment:

Full-time

Salary:

$41 per hour

City:

San Diego

Job Origin:

APPCAST_CPC

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Clinical Program ManagerPay Rate: $41.92–$54.48/hourDuration: 12-Month AssignmentHours: Full-Time, 40 hours per weekLocation: San Diego, CASummaryWe are seeking a Clinical Program Management professional to support clinical operations activities, study deliverables, documentation, data review, and cross-functional coordination.In this role, you will partner with clinical teams, vendors, sites, and internal stakeholders to help maintain accurate, timely, and compliant clinical work. The ideal candidate has experience supporting clinical processes, study coordination, documentation, and operational activities within established quality and regulatory expectations.What You'll DoSupport the planning, coordination, and execution of clinical activities and deliverablesMaintain study-related records, trackers, timelines, meeting materials, and documentation in accordance with established processesCoordinate information, communications, and follow-up with clinical teams, vendors, sites, and internal stakeholdersReview study documents, data, reports, and operational materials for accuracy, completeness, and consistencyTrack issues, action items, risks, and potential delays, and communicate relevant updates to appropriate stakeholdersSupport process updates, training coordination, and documentation needed to maintain clinical readinessParticipate in cross-functional clinical meetings and contribute to status updates and follow-up activitiesContribute to continuous improvement initiatives and efforts to strengthen clinical processesWhat You BringBachelor's degree in a related scientific, healthcare, business, or technical field, or equivalent education and experienceTypically 2+ years of relevant experience supporting functional projects, processes, analysis, documentation, or operationsKnowledge of clinical processes, documentation practices, and study coordinationFamiliarity with applicable quality or regulatory expectationsAbility to manage timelines, records, data, and stakeholder follow-up with accuracy and attention to detailStrong organizational skills and ability to follow established proceduresSound judgment and attention to detailStrong written and verbal communication skillsAbility to collaborate effectively across teams and functionsTCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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