Research Project Manager, Cancer & Hematology Clinical Research Program

BMC Software • Arlington, MA

1d • $61,500 - $89,500 • Onsite

About The Position

At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience. You’ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth. The Research Project Manager (RPM) is responsible for providing project management support in service to the overall execution of research initiatives within CH-CRP by all PIs across the program, including meeting necessary quality, and timeline targets, and supporting the development of research operational strategies and workflows in support of achieving program objectives. RPM will focus on establishing/maintaining standard operating procedures, policies to ensure department personnel/investigators are in compliance with research obligations, and applicable policies and regulations; oversee training of research personnel on new or revised SOPs/policies; ensure compliance with reporting to research funders and coordinate with internal and external collaborators. Also contributes to the start-up phase of new clinical trials by coordinating feasibility assessments and site selection processes. The Research Project Manager may be responsible for supervising interns, fellows, and junior research support staff.

Requirements

• Master’s degree in related field and minimum of three years’ experience in research public health, health care administration and/or related field, including experience managing projects and operations; or equivalent combination of education and experience.
• Must be highly organized and detail-oriented, have exceptional oral communications and writing skills.
• Demonstrated proficiency in project management, including budgeting, planning, execution, delivery, quality assurance, and reporting.
• Knowledge of MS Word, Power Point, and Excel is essential.
• Must be a proactive problem solver with superb planning, program coordination, and leadership skills.

Nice To Haves

• Experience in data analysis and manuscript preparation

Responsibilities

• Coordinates and facilitates the research project management life cycle, including initiation, development, and implementation of various complex programmatic oversight projects.
• Responsible for scoping, coordinating research oversight activities, training research staff to new workflows, and monitoring for compliance/performance.
• Coordinates research teams, and manages research project timelines, to ensure research trials or milestones are completed within the specified and in line with annual objectives.
• Meets regularly with stakeholders, including research staff, clients and study teams, to collect and communicate business and research requirements, and set expectations for research-related work.
• Works with Principal Investigators to select the most appropriate methodology and techniques for facilitating the research.
• Responsible for supporting the creation of qualitative and quantitative research plans, designing research questionnaires and moderator guides for investigator-initiated protocols
• Works with research teams (on site and/or off-site), and the project and research directors, to coordinate study initiatives, and conduct pre-research and post-research analyses and evaluations.
• Collects data, summarizes and interprets research/programmatic data and collaborates with Principal Investigator to author journal articles and to present findings at research seminars, study groups and conferences.
• Supervise CH-CRP Interns and Fellows including training, delegating tasks, overseeing daily activities, mentoring, guiding through demonstration of best practices and offering opportunities for professional development.
• Schedules and facilitates staff meetings. Plans agenda and ensures that minutes are taken, edited and distributed.
• Produces programmatic reports and presentations for various audiences, including staff, investigators, and executive leadership.
• Assists with development and writing of investigator-initiated proposals to obtain funding for ongoing and future research activities.
• Perform administrative duties, tracking and reporting programmatic-level adverse event compliance, data submission compliance, and other study management key performance indicators.
• Responsible for all other administrative duties related to research activities.

Benefits

• Competitive pay
• Tuition reimbursement and tuition remission programs
• Highly subsidized medical, dental, and vision insurance options
• Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
• Pioneering Research: Engage in groundbreaking research projects that are driving the forefront of biomedical science.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees