Clinical Operations Lead, Trials & Compliance

Verily Health; Dallas (TX); On-site; USD 119,000 - 179,000; Full time

Job summary

Verily Health is seeking a Clinical Operations Manager to drive end-to-end execution of clinical studies. You will own key documentation like protocols and ICFs, manage eTMFs, and coordinate with cross-functional teams to meet study milestones and regulatory requirements.

The role emphasizes a strong SME in clinical operations, GCP familiarity, and effective communication with sponsors, sites, and internal teams.

Qualifications

• 4+ years of direct experience in clinical operations or related role.
• Experience drafting clinical study documents (protocols, ICFs) and managing eTMF.
• Strong SME working inside cross-functional project teams.
• Excellent communication and organizational skills.

Responsibilities

• Author study documentation (protocols, ICFs, participant materials).
• Implement study operations plans (IQRMP, Study Monitoring Plan, SOPs).
• Serve as primary contact for clinical sites; manage site operations and IRB reporting.
• Oversee eTMFs to ensure GCP compliance and audit readiness.
• Support research timelines from inception to publication.

Skills

Cross-functional collaboration

SME in clinical operations

Communication skills

Project management

Education

Bachelor's degree in life sciences/healthcare/technical field

Tools

JIRA

Job description

Verily Health is seeking a Clinical Operations Manager to drive end-to-end execution of clinical studies. You will own key documentation like protocols and ICFs, manage eTMFs, and coordinate with cross-functional teams to meet study milestones and regulatory requirements.

The role emphasizes a strong SME in clinical operations, GCP familiarity, and effective communication with sponsors, sites, and internal teams.