Senior Clinical Trial Manager

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary The Senior Clinical Trial Manager (SCTM) is accountable for end-to-end study oversight and delivery at country level, ensuring adherence to timelines, budget and quality standards. The SCTM acts as the primary point of contact at a country level for both internal and external stakeholders, ensuring clear communication, effective coordination, and successful project execution.

Key Responsibilities

Leads local country cross functional teams and acts as the main point of contact for a country with global study team members. Leads the local country and site feasibility process, including proposal and validation of country study targets, as endorsed by country leadership. Plans, develops and executes timelines and activities for start-up in collaboration with the local study team, Global Trial Acceleration Centre (GTAC) and other relevant stakeholders. Plans, develops and executes country and site level patient recruitment strategy and risk mitigation. Coordinates and ensures country level study enrolment targets and timelines are met in collaboration with relevant stakeholders. Leads problem solving and resolution efforts including management of risk, contingencies, issue resolution and escalation to the appropriate stakeholder/s. Assessment and set up the of vendors during study start up period (locally) Investigator Meeting participation and preparation. Ensures data entered in the Clinical Trial Management System (CTMS) is current and complete, and access to eDC and vendor systems is available for the country and clinical trial site personnel. This includes entering necessary data and uploading documents in eTMF. Validation of study related materials (i.e. protocol, ICF, patient material). Supports the review of country and site-specific documents (e.g. ICF, patient material), and where applicable may include the preparation of site level ICF and other documents. May support preparation of materials for Site Initiation Visits. Responsible for verifying and confirming with local team eTMF completeness (Country and Site level). Prepare investigator sites to conduct clinical trials through the approval of Clinical Trial Package (CTP) documentation. Acknowledges Site Monitoring visit reports, takes action within the timelines specified and escalates issues and ensures appropriate documentation of issues. Coordination of database locks and query follow up. Ensures timelines are met. Ensure inspection readiness of assigned trials within country. Provide support to Health Authority inspection and pre-inspection activities. Coordinates, develops and writes the Corrective Actions / Preventive Actions (CAPA) and ensures implementation for Country audit level findings. Drives CAPA review, implementation and completion. Lead study team meetings locally. Supports GTAC in the resolution of queries related to site invoices and supports in the coordination of patient compensation claims (if applicable). Collaborates with the local study team to support the management of site relationships (may include CRO related issues). May support Investigator Site Assessment Visits (ISAs) and Site Initiation Visits (SIVs). May perform site closure activities, including post-close out. May act as point of contact for Sites. As required per country requirements, perform or support the preparation of submissions to Health Authorities including follow up until approval. This includes substantial amendments and any other documentation requiring HA submission. Perform submission to Ethics Committees and governance offices, where applicable, including follow up until approval (protocol, amendments/IB and any other documents requiring EC submission). Coordinate the MOH responses with regulatory and central teams, as applicable. May support the collection and distribution of documents to and from sites. Support the approval for the closure of funds/POs May update national registries where applicable. Serves as coordinating resource on country regulatory requirements and keeps up to date with evolving regulation in collaboration with Regulatory and Legal. Serves as a key resource for colleagues, by providing guidance, leading training and mentoring to other team members through a mentoring process using informal and/or formal presentations. Serves as a Subject Matter Expert (SME) in areas such as therapeutic area, systems or processes across the department with the opportunity to contribute at a regional or global level with this expertise. Competencies Thorough understanding of GCP, ICH Guidelines and Country regulatory environment. In-depth knowledge and understanding of clinical research processes, regulations, and methodology. Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management. Demonstrated organizational and planning skills and independent decision-making ability. Strong time management skills, and ability to effectively manage multiple competing priorities. Ability to think critically and analyze and react to risks. Strong communication skills with a strong customer focus, and ability to manage both internal and external clients at all organizational levels. Software that must be used independently and without assistance: Microsoft Suite, CTMS, eDC, eTMF Qualifications & Experience Bachelor's or Master's degree required. Field of study within life sciences or equivalent 6+ years' industry related experience Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiative Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives. Travel Required (nature and frequency) - Occasional local travel requirement Apply To This Job