$70K/yr – $85K/yr
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Job type
Salary
$70K/yr – $85K/yr
Location
Sector
Posted
17 days ago
Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical Trials
Tags
$70K/yr - $85K/yr
86
STRONG MATCH
Experience Level
72
Skill
100
Industry Exp.
65
Health Care
Social Media
Healthcare
Responsibilities
The Assistant Clinical Research Manager (ACRM) position will work within the Center of Early Detection & Intervention Blood Cancers (CEDI BC) Interventional Clinical Trials clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator
These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed
Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group’s clinical trial portfolio and all related regulatory and compliance requirements
The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group’s portfolio. They will be responsible for the required tracking of all protocol development, submission, review and approval milestones
The ACRM will assist with the oversight of subject enrollment, protocol treatment and follow-up care processes for protocol patients
Assist with the oversight of registration of protocol patients, study group registrar and pharmaceutical company as outlined in protocol
Assists in the responsibility for essential document compliance for entire portfolio. Implements systems to monitor and ensure regulatory document collection and maintenance compliance
Assists in the responsibilities for all clinical trial reporting requirements; safety event, annual approval, deviations etc. May implement systems to monitor portfolio compliance
Assists the study team to be maintain an “audit ready” research environment
Assists CRM with responsibility for data management and compliance for entire portfolio. Maintains schedules and procedures necessary for timely and complete data collection
Regularly reports data compliance status to key stakeholders; i.e. DFCI PI, study Sponsor, DFCI CTO. Helps to implement corrective action to maintain data compliance when necessary
Submits required “progress / tracking “reports to key stakeholders, when applicable
Will assist the CRM with the recruitment and oversight of coordinator staff as well as ensures that staff have completed mandatory training in a timely manner
Will help implement program specific on-boarding and orientation process and may participate in annual performance evaluations and competency assessments of research staff as needed
Will provide day to day supervision for study management staff, including clinical research coordinators, students, volunteers, and other research assistants as needed
Preferred
Minimum of 3 plus years of related experience preferred
Benefits
Hybrid work with 2-3 days per week onsite/remote; remote days may only be worked from a New England state (ME, VT, NH, MA, CT, RI).
Glassdoor
3.9
Dana-Farber Cancer Institute is a cancer research and treatment organization that provides specialized care for cancer patients.
Boston, Massachusetts, USA
http://www.dana-farber.org
Late Stage
Total Funding
$138.08M
Key Investors
Yawkey Foundation
Elaine and Eduardo Saverin Foundation
The DeGregorio Family Foundation
2026-06-09
Grant· $50M
2025-11-24
Grant· $20M
2025-05-06
Grant· $1M
Leadership Team
Benjamin Ebert
President and CEO
Prafulla Gokhale
Director, Lurie Family Imaging Center
Recent News
PR Newswire
Alpheus Medical Opens Enrollment in New Clinical Trial for Butterfly Glioblastoma
2026-10-08
Boston Globe
‘I feel like I’m collateral damage’: Mass General Brigham Health Plan removes Dana-Farber from its Medicare Advantage network
Qualifications
Must be able to perform day-to-day responsibilities independently with minimal supervision from managers
Has the ability to identify regulatory scenarios that require consultation
Has a good understanding of clinical trials start-up, active and close out phases
Has a good understanding of clinical research, local policy and federal regulation
Knowledge of cancer as a disease process, cancer treatment modalities, and the clinical trial process
In addition, has experience in protocol development, data compilation and analysis
The ACRM will have a good understanding of the various tracking systems used to ensure timely data management by the clinical research staff
They will also understand Federal and State regulations as they relate to research
Strong interpersonal, organizational and communication skills are required
Must have computer skills including the use of Microsoft Office
Bachelor's Degree required
Must have the ability to function independently, think critically and with good professional judgment
Minimum of 3 plus years of related experience preferred
Required skills
Clinical Research, Clinical Trial Management, Federal and State Research Regulations, Protocol Development, Data Analysis, Cancer Treatment Modalities, Microsoft Office
Preferred skills
Minimum of 3 plus years of related experience preferred
Experience
3+ years
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