Dana-Farber Cancer Institute

Translational Research Project Manager I

Dana-Farber Cancer Institute$79K — $91K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biology, biomedical sciences, public health, or a related discipline.
  • 3 years of experience in clinical research or project management, preferably in translational research.
  • Experience with basic project management tasks, including meeting coordination and documentation maintenance.
  • Background in academic institutions with a successful record in clinical research is preferred.
  • Familiarity with regulatory affairs, research ethics, and Responsible Conduct of Research is advantageous.

Responsibilities

  • Manage daily coordination and oversight of translational and biobanking research projects.
  • Assist Principal Investigator with grant applications and progress reports.
  • Ensure regulatory compliance for research activities by supporting protocol submissions and amendments.
  • Lead collaborative meetings to enhance communication among research teams.
  • Provide support in supervising research coordinators and staff involved in projects.
  • Coordinate day-to-day tasks of research projects, managing schedules and communications.

Benefits

  • Supportive work environment fostering collaboration and innovation.
  • Opportunities for professional development and growth within the field.
  • Flexible work hours to accommodate project demands.
  • Access to resources and tools necessary for project management.
Full Job Description
The Translational Research Project Manager I, TRPM I, oversees the daily coordination and management of translational and biobanking research projects, which involves collecting various biological samples and clinical data. This role supports grant applications, progress reports, project initiation, regulatory compliance, and patient identification for research projects. The TRPM I bridges clinical and laboratory research by supporting both types of investigators. Additionally, the TRPM I indirectly supervises research coordinators and independently manages a portfolio of projects for each investigator. The specific tasks and responsibilities of the TRPM I vary based on departmental and investigator needs.

  • Independent Project Management: Operate independently under the guidance of a senior manager, ensuring effective oversight and management of assigned projects. This involves coordinating various aspects of the project lifecycle, from initiation to completion, to meet research objectives.
  • Grant Support: Assist the Principal Investigator (PI) with grant applications and progress reports, playing a crucial role in securing funding for research initiatives. This includes gathering necessary data, preparing documentation, and ensuring timely submission to funding bodies.
  • Regulatory Compliance: Support the PI in meeting regulatory requirements, including protocol submissions, amendments, and deviation filings. This ensures that all research activities complies with legal and ethical standards, safeguarding the integrity of the projects.
  • Collaborative Meetings: Lead and participate in meetings with internal and external collaborators, fostering communication and collaboration among research teams. These meetings are essential for aligning project goals, sharing updates, and addressing any challenges that arise.
  • Staff Supervision Assistance: Assist Clinical Research Managers or Senior Translational Project Managers in supervising staff involved in project areas. This includes providing guidance, monitoring performance, and ensuring that team members adhere to project timelines and objectives.
  • Project Coordination: Responsible for the day-to-day coordination of research projects, ensuring that all tasks are executed efficiently and effectively. This involves managing schedules, resources, and communications to keep projects on track.


Knowledge, Skills and Abilities
  • Basic understanding of translational research principles and biobanking processes.
  • Basic knowledge of regulatory affairs, research ethics, and responsible conduct of research
  • Familiarity with grant application procedures and regulatory compliance requirements.
  • Basic understanding of data collection and management practices in research settings.
  • Awareness of ethical considerations in clinical research and patient data handling.
  • Strong organizational skills for managing day-to-day project tasks.
  • Effective communication skills for interacting with research teams and stakeholders.
  • Competency in using project management software and tools.
  • Ability to draft clear and concise reports and documentation.
  • Ability to work independently under general supervision.
  • Capability to assist with basic grant and regulatory documentation.
  • Ability to identify and resolve minor issues in project execution.
  • Capability to support the integration of clinical and laboratory research efforts.


Minimum Job Qualifications
  • Bachelor's degree is required, Biology, biomedical sciences, public health, or related discipline.
  • Three (3) years of experience in clinical research or project management, preference for experience in translational research projects.
  • Experience with basic project management tasks, such as coordinating meetings and maintaining documentation.
  • Experience in an academic institution with a proven track record of success in the clinical research field is preferred.
  • Experience in knowledge of regulatory affairs, research ethics, and Responsible Conduct of Research (RCR) is preferred.
  • Experience with basic grant writing and regulatory documentation is beneficial.


License/Certification/Registration Required: none

Supervisory Responsibilities: No

Patient Contact: None

The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications.

For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).

$79,400.00 - $91,900.00

About Dana-Farber Cancer Institute

Dana-Farber Cancer Institute is a non-profit organization that provides cancer treatment and research services. The institute was founded in 1947 and is affiliated with Harvard Medical School. Dana-Farber Cancer Institute is committed to providing the highest quality care to cancer patients, and is dedicated to finding new treatments and cures for the disease. The institute offers a range of services, including chemotherapy, radiation therapy, and surgery. Dana-Farber Cancer Institute is also involved in a number of research initiatives, and has made significant contributions to the field of cancer research.
Learn more about Dana-Farber Cancer Institute
Size
5,000 employees
Industry
Founded
1947

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