FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Clinical Operations Manager
VerilyClinical Operations Manager driving clinical study documentation, site operations, compliance, and closeout at Verily Health. Supporting precision-health research and evidentiary claim development across cross-functional teams.
Posted 8/5/2026full-timeDallas • California, Massachusetts, North Carolina, Texas • 🇺🇸 United StatesMid-LevelSenior💰 $119,000 - $179,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical operations, including drafting clinical study documentation and managing electronic Trial Master Files to ensure GCP compliance and regulatory adherence. Proven ability to drive project management initiatives and provide operational guidance within cross-functional teams.
Highest-signal resume keywords
Clinical Operations ManagementClinical Trial ManagementGCP ComplianceProject Management CertificationElectronic Trial Master File Systems
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Protocol DevelopmentInformed Consent Form DraftingQuality Risk ManagementStudy Monitoring PlansProtocol Deviation ManagementAdverse Event EvaluationIRB ReportingResearch Timeline ManagementEvidentiary Claim DevelopmentClinical SOP Development
Soft Skills
Excellent Communication SkillsStrong Organizational Skills
Tools & Technologies
JIRA
Certifications & Qualifications
Project Management Certification
Industry Keywords
Life SciencesHealthcareBiotechnologyRegulatory SubmissionCross-Functional Teams
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Serve as a dedicated clinical operations subject matter expert within a cross-functional team
- Drive core operational milestones from study design through study closeout
- Author and establish clinical protocols, informed consent forms, and participant-facing materials
- Implement integrated quality risk management and study monitoring plans alongside clinical SOPs
- Manage clinical site operations, protocol deviations, adverse event evaluations, and IRB reporting
- Oversee electronic Trial Master Files to maintain GCP compliance, regulatory adherence, and audit readiness
- Manage research timelines from inception through publication
- Provide project management support for evidentiary claim development projects across Research, EvGen, and Clinical Quality teams
Requirements
What you’ll need- Bachelor's degree in a life sciences, healthcare, or technical field, or equivalent practical experience
- 4+ years of direct experience in clinical operations, clinical trial management, or a related operational role within healthcare or biotechnology
- Direct experience drafting clinical study documentation, including protocols and informed consent forms
- Experience managing electronic Trial Master File systems
- Strong subject matter expertise working inside cross-functional project or product teams
- Deep familiarity with GCP compliance, regulatory submission considerations, and clinical SOP development
- Excellent communication skills for providing clear clinical operational guidance to cross-functional stakeholders
- Strong organizational skills supporting evidentiary claim development aligned with commercial needs
- Project management certification preferred
- Experience with JIRA preferred
- Must not require employer-sponsored work authorization now or in the future for employment in the United States
Benefits
Comp & perks- Bonus
- Equity
- Competitive benefits
- Flexibility, resources, and competitive benefits to support whole-person well-being
- Opportunities to grow
- Accommodation support for applicants