Clinical Trial Program Manager
tcwglobalSan Diego, CA
$54.48hr
Apply nowClinical Trial Program Manager
L4
tcwglobalSan Diego, CA3 days ago
$54.48hr
Industries
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)Research and Development in Biotechnology (except Nanobiotechnology)Other Scientific and Technical Consulting ServicesClinical Trial Program ManagerW2 Contract 12-Months, Possible Extension$54.48hr + Benefits San Diego, CA, 92103
Summary:
We 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 Do:
- Support the planning, coordination, and execution of clinical activities and deliverables
- Maintain study-related records, trackers, timelines, meeting materials, and documentation in accordance with established processes
- Coordinate information, communications, and follow-up with clinical teams, vendors, sites, and internal stakeholders
- Review study documents, data, reports, and operational materials for accuracy, completeness, and consistency
- Track issues, action items, risks, and potential delays, and communicate relevant updates to appropriate stakeholders
- Support process updates, training coordination, and documentation needed to maintain clinical readiness
- Participate in cross-functional clinical meetings and contribute to status updates and follow-up activities
- Contribute to continuous improvement initiatives and efforts to strengthen clinical processes
- What You Bring
- Bachelor's degree in a related scientific, healthcare, business, or technical field, or equivalent education and experience
- Typically 2+ years of relevant experience supporting functional projects, processes, analysis, documentation, or operations
- Knowledge of clinical processes, documentation practices, and study coordination
- Familiarity with applicable quality or regulatory expectations
- Ability to manage timelines, records, data, and stakeholder follow-up with accuracy and attention to detailStrong organizational skills and ability to follow established procedures
- Sound judgment and attention to detailStrong written and verbal communication skills
Ability 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.
Apply now
Level
MidL4
Salary
$54.48hr
Location
San Diego, CA
Occupation
Project Management Specialists
Industry
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
Posted
3 days ago
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