Translational Project Manager - Pediatric and Young Adult Cancer Cell Therapy

Overview

The Translational Research Project Manager (TRPM) will oversee the management of the Pediatric and Young Adult Cancer Cell Therapy Program at Dana-Farber Cancer Institute (DFCI) and Boston Children's Hospital (BCH). Working closely with program director Robbie Majzner, the TRPM will manage and direct the portfolio of novel cell therapies being brought to the clinic from the laboratories of DFCI and BCH. These therapies are designed to alter the standard of care and provide new therapeutic options to children and adults with incurable cancers. This role will encompass strategic decision making, program building, regulatory responsibilities, grant/report writing, and translational oversight to ensure effective translation of novel therapies at DFCI/BCH.

The successful applicant will possess a background in project and program management and regulatory sciences (optional but highly preferred), with excellent communication, organization, writing, and interpersonal skills and a passion for applying translational science toward the therapies of tomorrow.

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.

Project Management

1. Under the guidance of Dr. Majzner, strategizes on program goals and manages the implementation of program goals and objectives.

2. Manages project scope and timeline through formal change management processes.

3. Manages project issues and risks through standard issue/risk process.

4. Performs need assessments, evaluates and analyzes individual program and overall unit or department effectiveness; implements appropriate procedures to ensure efficiency and accuracy.

5. Manages relationships with funders and partners including cell manufacturing facility, other principal investigators, foundations, biotechs, and pharma partners; leads collaborative meetings; writes quarterly to yearly reports for funders, as required, and ensures deliverables are met.

6. Strategizes about program funding and assists in the preparation of grant applications.

7. Develops and facilitates or oversees the development and facilitation of workshops, seminars and orientations.

8. With program growth, may manage a team consisting of project managers and scientists.

9. Drafts business plans and strategic documents.

10. Performs regulatory tasks related to IND submissions and annual reports for clinical trials.

Knowledge, Skills, and Abilities Required

• Strong competencies in project management, planning, outsourcing, resource management and organization with the ability to coordinate multiple activities and resources, while maintaining a focus on quality.

• Ability to function effectively and independently in a fast-paced environment, organize and prioritize work, and meet deadlines.

• Familiarity with or interest/ability to rapidly become expert in PM software such as SmartSheets.

• Strong Emotional Intelligence (EQ).

• Enjoys working in an open academic environment.

• Excellent oral and written communication skills.

• Solid analytical capabilities and attention to detail.

• Ability to produce and present clear, concise, and professionally written communications and presentations.

Qualifications

• Bachelor's relevant degree with excellent project management and clinical research experience (5+ years) will be considered.

• Program and/or project management experience in a biotech/pharma and/or academic setting.

• Regulatory experience with clinical trial development preferred but not required.

Through proper management of our program, the TRPM will be an essential member of our team and a key contributor to our success in translating innovative science into the clinic.

At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are equally committed to diversifying our faculty and staff. Cancer knows no boundaries and when it comes to hiring the most dedicated and diverse professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.

Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.

EEOC Poster