The Clinical Document Management Specialist supports clinical trials by managing and processing essential documents to ensure compliance with SOPs and regulatory guidelines, assisting with TMF setup, maintenance, and close-out.

Manage clinical trial documentation, support clinical operations, ensure compliance with regulations, and facilitate communication with clinical sites.

The Clinical Research Associate I supports clinical research teams by training, document management, and ensuring compliance with protocols during clinical trials.

The Senior GCP Auditor ensures GCP compliance and interacts with teams to maintain audit readiness, manage incidents, and coordinate various audits while developing necessary documentation.

The Contracts Counsel will manage vendor and corporate contracts, support procurement and business operations, and provide legal advice on clinical and commercial matters.

The Sales Training & Development Director will lead training efforts for commercial operations, focusing on training curricula and effectiveness. Responsibilities include conducting training needs assessments, monitoring KPI effectiveness, and collaborating with analytics for targeted training.

Provide contract-related support through all phases of the contract lifecycle, collaborating with stakeholders, managing drafts, and ensuring compliance with SOPs.