Remote Clinical Operations Lead

Rho, Inc.; United States; Remote; USD 130.000 - 165.000; Vollzeit

Benefits dieser Stelle

Medical coverage

Vision coverage

Dental coverage

HSA

FSA

EAP

401(k)

Paid time off

Holidays

Parental leave

Bereavement leave

Zusammenfassung

Rho, Inc. in the United States is seeking a Clinical Team Lead II to drive clinical operations on our trials. You will own the operational aspects, mentor CRAs, ensure study protocols comply with ICH/GCP and regulations, and help manage timelines and budgets.

This remote-friendly position lets you lead site performance, develop monitoring plans, and collaborate with cross‑functional teams to deliver high-impact study outcomes and sponsor satisfaction.

Qualifikationen

• 8+ years of clinical research experience in CRO/pharma/biotech.
• 1-2 years leading the clinical operations function in trials.
• On-site monitoring experience preferred; travel up to 25%.

Aufgaben

• Drive project success with cross-functional study leadership.
• Identify and mitigate clinical risks; contribute to risk plans.
• Review study protocols and materials (e.g., CRF).
• Manage timelines, metrics, budgeting and resourcing.
• Develop monitoring tools and plans for studies.
• Oversee site performance in line with productivity goals.
• Create and conduct investigator meetings and trainings.
• Lead startup activities: site selection, supplies, progress tracking.
• Provide status updates to management and sponsors.
• Lead regular clinical team teleconferences.
• Coordinate with Site staff and escalate CRA issues.
• Document site decisions and mass communications.
• Participate in RFPs and business development meetings.
• Review monitoring visit reports and ensure contractual timing.
• Support PMs with project tasks and manage in-house CRAs.

Kenntnisse

Clinical ops leadership

Clinical monitoring

Project management

Cross-functional collaboration

Ausbildung

BA/BS in life science

Jobbeschreibung

Rho, Inc. in the United States is seeking a Clinical Team Lead II to drive clinical operations on our trials. You will own the operational aspects, mentor CRAs, ensure study protocols comply with ICH/GCP and regulations, and help manage timelines and budgets.

This remote-friendly position lets you lead site performance, develop monitoring plans, and collaborate with cross‑functional teams to deliver high-impact study outcomes and sponsor satisfaction.