Senior Director, Global Clinical Project Management - Oncology

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.Do not pass up this chance, apply quickly if your experience and skills match what is in the following description.We are seeking a highly skilled and motivated Senior Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The Senior Global Director, Clinical Project Management, will play a critical role in delivering high-quality data and ensuring the success of clinical studies.Key ResponsibilitiesOversee the planning and execution of global clinical trialsDevelop and implement study protocols, timelines, and budgetsManage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeoutEnsure compliance with Good Clinical Practice (GCP) and regulatory guidelinesCoordinate with cross-functional teams, including investigators, vendors, and regulatory bodiesMonitor trial progress and manage data collection to ensure accuracy and integrityIdentify and mitigate project risksOversee a team of regional CPMs, CRAs and CTAsEnsure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practiceConduct regular meetings with study teams and provide updates to stakeholdersCoordinate with external vendors and partners involved in the trialSupport development of key process initiatives and SOPs internallyOversee vendors supporting trial executionQualificationsBachelor's degree in Life Sciences, Nursing, or a related fieldMinimum of 15 years of experience in Clinical Trial Management, including demonstrated people leadership and direct line management experienceStrong experience working on early phase studies required, late phase studies experience is a plusStrong understanding of GCP and regulatory requirementsExcellent organizational and project management skillsProven ability to lead cross-functional teams and manage multiple prioritiesStrong communication and interpersonal skillsAbility to work collaboratively in a team-oriented environmentFlexibility and adaptability to changing priorities and workloadLocation/Travel:Princeton NJ hybrid, 3 days in officeOvernight travel ~25%The expected base salary range for this position is $220,000 - $280,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.We offer an opportunity for you to learn and grow while making significant contributions to the company's success.SystImmune is an Equal Opportunity Employer. xhyhwjd We welcome diverse talent and encourage all qualified applicants to apply.