Clinical Project Scientist – Oncology The Clinical Project Scientist leads the design, planning, implementation, monitoring, and reporting of clinical research trials in oncology.Location: Raritan, New Jersey, United States of America

Responsibilities Partner with the Study Responsible Physician (SRP) to provide clinical oversight to the study.

Develop clinical research protocols, study case report forms, and informed consent documents.

Develop the medical review plan to support the statistical analysis plan.

Play a key role in medical review of study data, assisting in coding, analysis, and documentation.

Validate and interpret results of phaseII‑IV investigations for preparation of new drug applications, scientific congresses, and peer‑reviewed journals.

Ensure team members adhere to clinical research guidelines, safety procedures, and communicate detailed outcomes and results of research findings to relevant partners.

Provide input in managing project budgets and projections.

Serve as liaison to global clinical sites for medical questions related to the clinical research trial.

Present study status at internal and external meetings, including investigator meetings and governance committees.

Train and mentor local/central study teams and investigative sites on the study protocol, ensuring they have the necessary guidance and tools for performance of project activities.

Participate in or lead interactions with health authorities.

Maintain expertise on clinical trial documentation, regulatory requirements, operational procedures, and study file requirements.

Review and maintain correct standard operating procedures, procedures, and protocols.

Qualifications Master’s Degree, Ph.D., Pharm.D., or a B.A./B.S. with commensurate exceptional clinical research experience.

Minimum of 3 years of industry experience in Oncology.

Significant knowledge of basic and translational research with an understanding of applications to cancer drug development.

Ability to work in a matrix team environment, with adherence to the highest personal and ethical standards and a commitment to patient‑centered clinical research.

Preferred Skills Clinical Evaluations

Corrective and Preventive Action (CAPA)

Drug Discovery Development

Entrepreneurship

Good Clinical Practice (GCP)

Leadership

Medicines and Device Development and Regulation

Presentation Design

Regulatory Affairs Management

Relationship Building

Research Documents

Safety‑Oriented

Scientific Research

Strategic Change

Study Management

Tactical Planning

Technical Credibility

Compensation &

Benefits Base pay: $122,000 – $212,000 (US‑based). Eligible for an annual performance bonus in accordance with the applicable plan. Company‑sponsored benefits include medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, and group legal insurance. Eligibility for a 401(k) plan, long‑term incentive program, and pooled bonuses. Time‑off: vacation up to 120 hours per calendar year, sick time up to 40 hours per calendar year, holiday pay (including floating holidays) up to 13 days per calendar year, and work, personal and family time up to 40 hours per calendar year.

EEO Statement 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 any other characteristic protected by federal, state, or local law. We actively seek protected veterans and individuals with disabilities.