In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. You will oversee local trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations.

This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.

Key Responsibilities

Clinical Trial Delivery & Oversight
• Lead end-to-end country-level trial management, from study start-up through database lock and closeout
• Serve as the primary contact for assigned clinical trials within your country
• Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
• Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target

Site & Stakeholder Management
• Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study execution
• Lead site feasibility, selection, and activation processes
• Drive investigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance
• Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
• Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
• Oversee patient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management
• Manage country-level budgets, forecasting, and financial tracking
• Oversee local vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance
• Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
• Ensure compliance with local regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications
• Bachelor's degree in life sciences, healthcare, or related field
• Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
• Excellent communication and stakeholder management skills
• Proficiency in clinical systems (e.g., CTMS, eTMF)
• 3-5+ years of total trial management experience
• Experience managing complex or early-phase trials
• Demonstrated ability to lead cross-functional teams and drive performance

The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.