Clinical Trial Manager

Role: Clinical Trial Manager (CTM) responsible for end-to-end operational oversight of clinical studies at the country level, ensuring adherence to timelines, budgets, and quality standards. Responsibilities: act as primary contact for stakeholders, coordinate with local cross-functional teams, manage study start-up, patient recruitment, site preparation, data management, and regulatory submissions; oversee vendor setup, site monitoring, and inspection readiness; support audits and CAPA processes; and facilitate communication between sites, global teams, and regulators. Requirements: Bachelor's or Master's in Life Sciences or related field; minimum 4 years' industry experience in clinical operations; deep knowledge of GCP, ICH guidelines, and local regulations; proficiency in CTMS, eDC, and eTMF systems; strong organizational, decision-making, and communication skills; experience leading cross-functional initiatives and mentoring team members. HighValue: focus on global or country-specific clinical trial execution, regulatory compliance, site management, and stakeholder coordination; expertise in GCP, clinical landscape, and documentation validation. WorkSetup: local travel <1 month/quarter; role supports hybrid or onsite work in the U.S.