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    Translational Project Manager - Pediatric And Young Adult Cancer Cell Therapy

    Dana Farber Cancer Institute
    5+ years
    Not Disclosed
    Boston
    10 Nov. 7, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Translational Research Project Manager (TRPM) - Pediatric & Young Adult Cancer Cell Therapy

    Location: Boston, MA
    Organization: Dana-Farber Cancer Institute & Boston Children's Hospital

    Position Overview:

    The Translational Research Project Manager (TRPM) will oversee the Pediatric and Young Adult Cancer Cell Therapy Program at Dana-Farber Cancer Institute (DFCI) and Boston Children’s Hospital (BCH). In collaboration with program director Dr. Robbie Majzner, the TRPM will manage a portfolio of novel cell therapies aimed at altering the standard of care and providing innovative therapeutic options for children and adults with incurable cancers. This role involves strategic decision-making, regulatory oversight, program management, grant/report writing, and translational research oversight, ensuring the successful translation of cutting-edge therapies from the laboratory to the clinic.

    Dana-Farber Cancer Institute, located in Boston, is a leader in groundbreaking cancer research and patient care. We are united by our mission to conquer cancer, HIV/AIDS, and related diseases. Our goal is to foster an inclusive, diverse, and equitable environment that provides compassionate care to all patients, promotes public health in high-risk communities, and advances medical knowledge through innovative research.

    Key Responsibilities:

    Project Management:

    • Work closely with Dr. Majzner to strategize and implement program goals and objectives.
    • Manage project scope and timelines through formal change management processes.
    • Address project issues and risks, applying standard risk management techniques.
    • Perform needs assessments and evaluate the effectiveness of the program, implementing solutions to improve efficiency and accuracy.
    • Manage relationships with external funders, collaborators, and industry partners (biotech, pharma, etc.).
    • Lead collaborative meetings and ensure deliverables are met according to agreed-upon timelines.
    • Assist in program funding strategies and grant applications.
    • Develop and lead workshops, seminars, and orientations for the program.
    • Draft strategic documents, including business plans and reports for stakeholders and funding partners.
    • Supervise and guide junior research staff, including Project Managers, Clinical Research Coordinators, and Research Assistants.

    Regulatory Oversight:

    • Support regulatory tasks related to IND submissions and annual reports for clinical trials.
    • Ensure compliance with regulatory requirements throughout the clinical trial process.

    Team Leadership & Supervision:

    • Assist with the supervision of research staff, including potential direct reports such as Translational Research Project Managers, Clinical Research Coordinators, and Research Technicians.
    • Provide mentoring and oversight to junior team members as needed.

    Patient Contact:

    • Assist with patient consenting in research protocols in collaboration with Clinical Research Coordinators and Data Specialists.

    Qualifications:

    Education:

    • Bachelor's degree in a relevant field (e.g., clinical research, life sciences, or a related discipline).

    Experience:

    • At least 5 years of clinical research experience, including a minimum of 3 years in project management.
    • Experience in program/project management within a biotech, pharma, or academic research setting.
    • Regulatory experience with clinical trial development is preferred but not required.

    Skills & Abilities:

    • Strong competencies in project management, resource management, and organization, with the ability to coordinate multiple tasks and resources effectively.
    • Ability to thrive in a fast-paced environment, with excellent organizational and prioritization skills.
    • Proficiency with project management software such as SmartSheets (or ability to quickly learn such tools).
    • High emotional intelligence (EQ) and a collaborative work style.
    • Excellent written and verbal communication skills, with the ability to produce clear, professional reports and presentations.
    • Solid analytical and problem-solving capabilities, with a keen attention to detail.

    Additional Information:

    Dana-Farber Cancer Institute is committed to creating an inclusive environment where diversity is celebrated. We encourage applicants from all backgrounds to apply, as we strive to reduce the burden of cancer for all people. We are an equal opportunity employer and welcome applicants regardless of race, color, religion, gender identity, sexual orientation, disability, or any other characteristic protected by law.

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