Sr./Clinical Trial Manager
Company: Ladders Agency
- Location: United States
- Work mode: Remote
- Seniority: Senior
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
For our client, we are seeking a Sr./Clinical Trial Manager to join the team of a leader in the Pharmaceuticals & Biotech space.
This role will drive operational execution across clinical studies, with a strong focus on planning, vendor management, financial oversight, and site activation. The person in this position will partner closely with internal stakeholders, CROs, clinical sites, and external vendors to keep studies on track from start-up through monitoring and closeout. This is a highly cross-functional role supporting complex programs in a fast-moving biopharmaceutical environment. Experience with global trials, immunology, or rare disease programs would be especially valuable.
Location: Remote
Compensation: $180,000 – $195,000 annually
Responsibilities
- Support development and execution of detailed study operational plans and timelines
- Oversee vendor activities, including performance metrics and issue resolution
- Maintain clinical trial budgets, track spending, and escalate financial risks
- Manage study risk and issue logs, driving resolution activities
- Coordinate input for clinical documents such as protocols and monitoring plans
- Oversee global study start-up, site activation, and monitoring activities
- Build relationships with clinical sites, CROs, and internal stakeholders
Qualifications
- Bachelor's degree with 10+ years of experience for Sr. Clinical Trial Manager or 7+ years for Clinical Trial Manager
- Experience in trial management within a biopharmaceutical company; startup experience is a plus
- Proven track record in managing complex clinical trials from Phase 1 to Phase 3, with global experience preferred
- Preferred experience in immunology and/or rare disease clinical trials
- Strong background in managing CROs and clinical vendors, including labs and clinical technology
- In-depth knowledge of FDA regulations, ICH guidelines, and Good Clinical Practice
- Excellent communication, organization, and problem-solving skills, with a focus on detail
Benefits
- Remote work flexibility with periodic travel for team events
- Opportunity to contribute to the company's immunology pipeline
- Mentorship opportunities for junior team members
- Engagement in a dynamic and collaborative work environment
Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.
