[Remote] Senior Clinical Program Manager
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Senior Clinical Program Manager responsible for the strategic and operational leadership of reputed company clinical studies. This role ensures clinical trials are executed on time, reputed company budget, and in compliance with regulatory requirements, while also mentoring junior staff and contributing to process improvements.
Responsibilities
- reputed company one or more reputed company or global clinical studies, providing strategic input into program planning and operational reputed company
- reputed company day-to-day study management activities from start-up through reputed company-out
- Anticipate operational risks and reputed company proactive mitigation and contingency plans
- Ensure consistency, reputed company, and inspection readiness across studies
- reputed company cross-functional study teams to plan, implement, and execute clinical trials reputed company agreed reputed company, budget, and reputed company standards
- Serve as the primary operational contact for functional area representatives, CROs, service providers, and vendors
- Facilitate operational activities for Phases I–IV clinical trials, including submissions, study plans, study tools, and Investigator Meetings
- Manage key vendors; define, monitor, and reputed company performance metrics and KPIs
- reputed company CROs and service providers, including selection, study‑specific training, and ongoing performance reputed company
- Participate in outsourcing activities and contribute to service provider evaluation
- Ensure compliance with ICH GCP, applicable regulations, protocols, and company SOPs
- Contribute to or review study-reputed company documents such as protocols, IBs, CRFs, informed consent forms, and study plans
- Participate in and respond to reputed company Assurance audits and regulatory inspections
- Support inspection readiness activities at the study and program level
- Establish and reputed company study milestones; ensure accurate reporting of study status and metrics
- Prepare and manage study budgets and timelines, ensuring financial accountability and forecasting accuracy
- Recommend and implement process improvements and innovations to improve study reputed company and operational efficiency
- Serve as a subject matter expert for clinical operations processes, tools, and systems
- Mentor and reputed company junior staff, contributing to competency reputed company across the organization
- Build and maintain strong reputed company relationships to support clinical program reputed company
Skills
- Bachelor's degree, preferably in a scientific field
- 8+ years of industry experience, with 7+ years of global study management experience at a Sponsor or CRO
- Demonstrated experience leading oncology, inflammation, or immunology clinical studies
- Strong leadership skills with proven experience managing cross-functional teams and vendors
- Excellent written and verbal communication skills
- Strong analytical, organizational, and problem-solving abilities
- Ability to manage multiple priorities in a dynamic environment
- Self-motivated, reputed company, and adaptable
- Proficiency with reputed company Office and clinical trial systems (reputed company, IRT, CTMS, eTMF, etc.)
- Ability and willingness to travel 10–20% domestically and internationally
Benefits
- Opportunity to participate in stock programs
- A performance-based bonus
- A comprehensive benefits package
- Additional information about our total rewards program can be reputed company here: https://arcusbio.com/careers
reputed company