Cullinan Oncology

• Serves as the medical monitor for clinical trials and assists in resolving major issues that may affect their assigned studies. • Partners with the Clinical Scientist, Data Manager, Pharmacovigilance Scientist, and other members of the study team to conduct the clinical studies, including study design, operational feasibility assessment, and site selection. • Provides expert opinion and review for creation of key study documents, including clinical study protocols, safety and medical monitoring plans, charters, and informed consent forms. • Interacts closely with Regulatory Affairs to contribute or review clinically relevant components of investigator brochures, briefing books, and other regulatory documents and communications. • Conducts investigator meetings, leads site initiation visits, and maintains relationships with clinical trial investigators. • Works with internal discovery and translational scientists, technical operations/manufacturing teams, regulatory affairs, safety and pharmacovigilance, and external consultants or CROs in a cross-functional manner. • Oversees and supports the gathering, analyzing, reviewing, interpreting, and reporting of clinical safety and efficacy data. • Supports publication and external communication strategy, acting as owner of clinical data, collaborating in the creation of meeting abstracts, presentations, and publications, and presenting at investigator meetings and scientific conferences as required.

Cullinan Therapeutics is a biopharmaceutical company developing potential first- or best-in-class, high-impact therapies for autoimmune diseases and cancer. Cullinan pursues promising therapeutic targets while leveraging core expertise in T cell engagers, which are established in oncology and are now advancing into autoimmune diseases. With a clinical-stage pipeline built on a rigorous scientific approach and purposeful innovation, Cullinan is advancing its mission to deliver new standards of care for patients. The Pharmacovigilance Scientist (PVS) participates in the development and planning of safety strategies for assigned products in early clinical development (Phase I and II clinical studies). This will include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment. PVS will play essential role in developing PV/Safety documents in collaboration with other PV team members and cross-functional teams e.g., medical, clinical operations, biostatistics, and regulatory affairs. Position Responsibilities Provide complete Cullinan product life-cycle support for assigned product(s) and participate in clinical study team meetings as appropriate for assigned products Represent PV for assigned compounds as a PV lead in cross-functional teams, including Cullinan Safety Management Team (SMT), Safety Review committee (SRC) and other teams with members external to Cullinan. Perform ongoing quality review of ICSR representing company review in accordance with study Safety Management Plans, Safety exchange agreements, and SOPs. Perform signal detection activities for assigned products in line with approved safety surveillance plan. Perform signal evaluation for any identified signals and author the safety evaluation report. Ensure timely, quality reports/safety analyses related to core deliverables with oversight as appropriate. Analyze the safety data, prepare and deliver presentations at SMT meetings. Responsible for authoring, preparation and review of safety documents including DSUR, response to health authority or other stakeholder safety queries etc. Collaborate with clinical/Medical team to foster communication of potential safety concerns. Alert the Head of PV and Medical Safety Physicians to potential safety issues recognized through single case medical review or aggregated data sets. Participate and collaborate with the Clinical/Medical team in other risk management/mitigation activities in the clinical studies as appropriate for assigned compounds. Responsible for authoring the RSI section of the IB with an ability to provide expectedness of events for regulatory reporting purposes. Responsible for authoring the safety section in collaboration with team members on regulatory responses, IBs, review Informed Consent Forms (ICF), CRFs, and providing the necessary quality control for safety assessment. Participate and collaborate with Clinical/Medical function in the development of protocols, and ensure safety oversight in cooperation/leadership of the clinical trial medical team Ensure timely, quality reports/safety analyses related to core deliverables with oversight as appropriate. Serve as a Pharmacovigilance resource to the cross-functional teams. Collaborate with clinical/Medical team to foster communication of the potential safety concerns. Able to work with and collaborate with Pharmacovigilance Operations (PVO) to manage PV related activities by CRO. Participate and collaborate with PVO for SAE reconciliation activities between the clinical and safety databases in accordance with SOPs. Participating in and collaborating with PVO in the process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents. Review and provide input and support with other departments (e.g., clinical/medical, clinical operations, medical information, regulatory affairs, and data management) groups on PV-related topics for study protocols, statistical analysis plans, and other clinical-related documents. Candidate Requirements Compensation The salary range for this role is $210,000 - $270,000. The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Actual base salary pay for the role may vary within the range based on several factors including, but not limited to, geographic location, candidate experience, skills, relevant education/qualifications, competencies, external market, internal equity, business needs and/or other job-related factors permitted by law. Additional compensation/benefits include annual bonus opportunity (25% of salary), annual equity awards, medical, dental, vision, life and disability insurance, 401(K) plan with employer match, stock options, employee stock purchase plan, flexible non-accrual paid time off, paid holidays, end-of-year shut down, cell phone reimbursement, tuition reimbursement, paid parental leave. Cullinan Therapeutics is proud to be an Equal Opportunity Employer. We are committed to creating an inclusive and diverse environment for all employees and applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.