Remote Clinical Trials Manager - 210641

Responsibilities:

• Assist in site selection, create RFPs, negotiate contracts, manage budgets, and oversee invoicing.
• Efficiently oversee clinical trials, managing multiple studies within a development program.
• Train team members and partners, maintain study files, provide regular updates to management, and ensure compliance with GCP.
• Participate in audits, maintain Trial Master Files, and attend Investigator Meetings and site visits as required.
• Lead study teams, foster relationships with external partners (CROs, labs, IRBs, sites), and identify/manage risks.
• Coordinate trial activities, review and contribute to study documents, and organize cross-functional meetings.

Requirements:

• Hold a Bachelor's degree in life sciences or a healthcare field.
• Show experience in international trials and managing external providers, including CROs.
• Possess a minimum of 7 years of clinical trial management experience, with a focus on recent Oncology trials.
• Demonstrate proficiency in GCP, FDA, and ICH regulations.