Associate Director, Clinical Project Scientist, Oncology Full-time NEW

Clinical Project Scientist

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

The Clinical Project Scientist is responsible for the design, planning, implementation, monitoring, and reporting of clinical research trials. The following responsibilities will be demonstrated in varying degrees of participation and leadership:

• Partners with Study Responsible Physician (SRP) to provide clinical oversight to the study;
• Develops clinical research protocols, study case report forms, informed consent;
• Develops the medical review plan to support the statistical analysis plan;
• Plays a key role in the medical review of the study data and assists in coding, analysis and documentation
• Validates and interprets results of phase II – IV investigations in preparing new drug applications to the appropriate health authorities, scientific congresses, and peer-reviewed journals
• Ensures team member adherence to clinical research guidelines and safety procedures;
• Communicates detailed outcomes and results of research findings to relevant partners;
• Provides input in managing project budgets and projections;
• Serves as liaison to global clinical sites for medical questions related to the clinical research trial ;
• Presents study status at internal/external meetings, including investigator meetings and governance committees
• Trains and mentors local/central study teams and investigative sites on the study protocol, ensuring they have the necessary guidance and tools for performance of various project activities
• Participates in/leads interactions with health authorities;
• Maintains expertise on clinical trial documentation, requirements, regulations, operational procedures, study file requirements, regulatory requirements, policies;
• Reviews and maintains correct standard operations, procedures and protocol

Qualifications – Internal

• A Master's Degree, Ph.D., Pharm.D., or a B.A./B.S. with commensurate exceptional clinical research experience is required.
• A 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 is required.
• The ability to work in a matrix team environment and adherence to the highest personal and ethical standards with a commitment to patient-centered clinical research is required.

The anticipated base pay range for this position is $122,000 – $212,000. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.

• Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
• Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
• This position is eligible to participate in the Company's long-term incentive program.
• Employees are eligible for the following time off benefits:
• Vacation – up to 120 hours per calendar year
• Sick time – up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
• Holiday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time – up to 40 hours per calendar year
• Additional information can be found via the following link: https://www.careers.jnj.com/employee-benefits

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. 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 Section 503 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 https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

Required 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

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

The anticipated base pay range for this position is: $137,000.00 – $235,750.00

Additional Description for Pay Transparency: