Clinical Operations Associate Manager

Title: Clinical Operations Associate Manager Company: Ipsen Korea About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society! For more information, visit us at and follow our latest news on LinkedIn and Instagram . Job Description: To lead and oversee the operational execution of global and local clinical studies in Korea, including company-sponsored studies and investigator-sponsored studies, in accordance with Ipsen SOPs, applicable local regulations, ICH-GCP, GPP, GPvP, and internal compliance standards. The role acts as the local clinical operations lead and serves as the primary local study operations contact for assigned studies, ensuring effective planning, implementation, monitoring oversight, vendor coordination, study budget tracking, study documentation oversight, and timely delivery of clinical study milestones. This position works closely with Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality, Legal, Finance, global/regional Clinical Operations teams, external vendors, study sites, investigators, and other relevant stakeholders. Main Responsibilities Clinical study planning and local feasibility Lead local operational planning for assigned global and local studies in Korea, including feasibility, site selection, timelines, milestones, budget assumptions, vendor needs, and operational input to study documents. Partner with Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality, and global/regional teams to ensure study start-up readiness. Implementation and oversight of clinical studies Oversee study start-up, conduct, monitoring follow-up, enrollment progress, issue escalation, CAPA/mitigation actions, and close-out to deliver study milestones on time. Coordinate required study documents and serve as a key local operational contact for study sites, vendors, IRBs/IECs, authorities, and internal stakeholders. Vendor, CRO, CRA and site oversight Oversee vendors, CROs, CRAs, consultants, study sites, and service providers against agreed milestones, deliverables, quality expectations, and contractual obligations. Support vendor/site selection, financial agreement processes, and monitoring oversight in collaboration with Medical Affairs, Procurement, Legal, Quality, Finance, and other relevant teams. Study budget, contract and resource management Develop, track, and monitor study budgets, costs, resources, timelines, contracts, payments, and operational deliverables, escalating significant risks or discrepancies as needed. Study documentation, systems and quality compliance Ensure study documentation, CTMS/system updates, milestone tracking, and essential documents are accurate, complete, timely, and inspection ready. Maintain compliance with Ipsen SOPs, ICH-GCP, GPP, GPvP, and local regulatory requirements, and support audits, inspections, quality reviews, and follow-up actions. IMP and study material coordination Coordinate IMP, trial materials, and study supplies planning, forecasting, supply, handling, reconciliation, and documentation with global/regional supply chain and relevant stakeholders. Cross-functional collaboration and governance Serve as local clinical operations lead, ensuring effective communication, governance updates, decision support, and timely escalation of study risks, issues, resource constraints, and timeline delays. Drive alignment across Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality, Legal, Finance, Procurement, global/regional Clinical Operations, and external partners. Local clinical operations capability Strengthen local clinical operations capability by supporting onboarding, training coordination, system access. Technical Competencies Clinical project management and execution oversight across the study lifecycle. Ability to identify, assess, escalate, and mitigate operational risks impacting timelines, quality, budget, or compliance. Vendor, CRO, and service provider oversight to ensure delivery against contractual obligations and study objectives. Strong understanding of clinical quality systems, inspection readiness, audit support, and CAPA management. Effective stakeholder management and cross-functional collaboration in a matrix environment. Working knowledge of CTMS and clinical documentation management practices. Knowledge & Experience: Minimum 5 years of overall professional experience, including at least 3 years of relevant experience in clinical operations, clinical trial management, clinical project management, or related clinical research roles. Experience managing or supporting global and/or local clinical studies from planning through study close-out. Experience working with CROs, investigators, study sites, and external vendors. Knowledge of Korean clinical trial regulations, ICH-GCP, and related compliance requirements. Experience supporting inspections, audits, quality reviews, or compliance-related activities Knowledge & Experience (preferred): Experience with both company-sponsored studies and investigator-sponsored studies in Korea. Experience working in a matrix, regional, or global clinical operations environment. Experience in specialty care, oncology, rare disease, or other complex therapeutic areas. Education / Certifications: Bachelor’s degree in life sciences, pharmacy, nursing, public health, clinical research, or a related scientific/healthcare discipline. Education / Certifications (preferred): Advanced degree or professional training/certification in clinical research, GCP, project management, regulatory affairs, or quality management. Language(s): Fluent Korean and business-level English, with the ability to communicate effectively with local stakeholders and global/regional teams. Additional language capability relevant to regional or global collaboration is an advantage. #LI-Hybrid #LI-CT1 We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.