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
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