Job Overview We are searching for the best talent for a Director, Clinical Sciences Oncology to provide active scientific and strategic contributions and leadership in a hybrid-based office located in either Spring House, PA; Raritan, NJ; or San Diego, CA. Remote based options within the USA may be considered on a case‑by‑case basis and if approved by the company. This role involves collaborating with cross‑functional teams, in close partnership with Study Responsible Physicians/Clinical Leads, to design, plan, and manage complex clinical trials while ensuring compliance with departmental, company, and regulatory standards. Responsibilities Drive clinical development strategy, contribute to the development of study‑related materials (e.g., ADP, SAP, CSR outputs, case report forms, operational plans), and represent the study in review committees. Lead the execution of clinical trial protocols within the clinical development program, ensuring compliance with scientific, organizational, and regulatory standards. Oversee end‑to‑end delivery of clinical trial protocols/programs, including study design, initiation, medical safety data monitoring, data dissemination, and closeout activities. Manage and coordinate activities with internal functional partners and external partners to ensure time‑to‑completion of clinical studies. Maintain the quality and integrity of clinical data critical to the evaluation of study endpoints. Interact and collaborate with investigators and study teams during the conduct of the trial(s). Lead training on study protocol, disease evaluation criteria, and other essential components to enhance understanding of clinical development processes. Review, interpret, and report clinical trial data, ensuring accuracy and integrity for health authority submissions. Draft documents for reporting clinical trial data (e.g., clinical study reports, patient narratives, investigator brochures, and periodic safety updates). Collaborate with Study Responsible Scientist and Study Responsible Physician to assess and evaluate clinical trial medical/safety data. Establish and define medical data review plan in partnership with Study Responsible Physician. Perform medical data monitoring/reporting and evaluate ongoing clinical trial data. Act as a liaison between the company and clinical investigators, fostering collaborations with key opinion leaders and external advisors. Develop and maintain credible relationships with internal and external stakeholders, including senior management, cross‑functional trial teams, and external partners/vendors. Provide mentorship and training to junior team members, fostering a collaborative work environment. Identify opportunities for process improvements and drive the implementation of best practices in clinical trial execution. Drive innovative research methods and operational strategies to enhance clinical development efficiency. Collaborate with cross‑functional partners to align clinical strategies with overall product development goals. Participate in governance meetings and cross‑functional initiatives to promote business strategies and process improvements. Prepare and present findings and results of clinical research at internal and external meetings. May act as an author for scientific publications, as applicable, to influence clinical development practices and advancements. Research and review medical literature and new technologies to support operational planning and scientific strategy implementation. Integrate scientific and technological innovations into clinical trial designs, including biomarkers and digital health initiatives. Qualifications Minimum bachelor’s degree in a scientific or related discipline; advanced degree (MS, PharmD, PhD) preferred. 10 years of relevant experience in clinical research and development within the pharmaceutical industry, biotech, CRO, or equivalent. Oncology experience preferred. Strong understanding of clinical development processes (trial design, protocol development, data analysis, regulatory guidelines, Good Clinical Practice). Proven experience managing all aspects of clinical trials from conception to closure, including data management and quality assurance practices. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint) and familiarity with generative artificial intelligence and clinical trial management software advantageous. Excellent written and verbal communication skills in English; ability to present information and negotiate with stakeholders. Excellent interpersonal skills with a collaborative approach to working within cross‑functional and global matrix teams. Exceptional organizational skills, ability to manage multiple tasks, prioritize effectively, and respond to changing business needs. Proven analytical and problem‑solving capabilities with a detail‑oriented mindset. Ability to proactively identify program‑level issues requiring escalation and to handle complex projects to overcome delays and obstacles. Experience leading scientific teams, providing mentorship, and managing direct or indirect reports. Willingness to travel domestically and internationally, approximately 10%, as required by project needs. Commitment to maintaining high ethical standards and fostering a culture of inclusivity in the workplace. Location and Availability Hybrid-based office located in either Spring House, PA; Raritan, NJ; or San Diego, CA. Remote options within the USA may be considered on a case‑by‑case basis, subject to approval by the company. Equal Employment Opportunity Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource. #J-18808-Ljbffr