KPS Life is seeking a Senior Clinical Trial Manager to join our Clinical Operations team. Sponsor dedicated , 1 FTE , 1 year contract, remote role, travel up to 25 %
In this pivotal role, you’ll lead and oversee clinical trials. From trial start-up through CSR, you’ll be responsible for managing documentation, training, vendor oversight, site-level activities, and ensuring timely delivery of high-quality data.
This is a non-supervisory position, but you’ll play a key role in guiding vendors and contractors to success.
Key Responsibilities
- Lead and coordinate all clinical trial activities in compliance with GCP and regulatory guidelines
- Manage regional trial operations and global site-level monitoring
- Oversee third-party vendors to ensure quality, cost, and timeline goals are met
- Collaborate with cross-functional study teams to drive project deliverables
- Track study metrics and ensure performance standards are achieved
- Develop trial documentation and provide regular updates to senior management
- Support contract management, including scope changes and change orders
- Mentor CRAs and CTAs, fostering growth and leadership
- Partner with Clinical Scientists and Development Leads to review patient data
- Contribute to SOP development and process improvement initiatives
Qualifications
- Bachelor’s degree in life sciences, healthcare, or related field
- 8+ years of clinical trial management experience in pharma/biotech
- Experience in rare disease and/or orphan indications preferred
- Proven ability to manage large, complex studies and cross-functional teams
- Strong vendor management experience (CROs and specialty vendors)
- Deep understanding of ICH/GCP and global clinical trial regulations
- Excellent leadership, communication, and organizational skills
- Critical thinking and proactive problem-solving mindset
Apply today and help shape the future of clinical research #kpslife
