Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers In[...]

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. This position’s work location is hybrid with two or three days per week onsite/remote. The selected candidate may only work remote days from a New England state (ME, VT, NH, MA, CT, RI). Clinical Trials Operations 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 with all aspects of study start‑up, active and close‑out activities for the group’s portfolio and 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. Regulatory & Compliance Assists in the responsibility for essential document compliance for the entire portfolio and 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., and may implement systems to monitor portfolio compliance. Assists the study team to maintain an “audit‑ready” research environment. Data Management & Clinical Trial Monitoring Assists CRM with responsibility for data management and compliance for the entire portfolio, maintaining schedules and procedures necessary for timely and complete data collection. Regularly reports data compliance status to key stakeholders (e.g., DFCI PI, study sponsor, DFCI CTO) and helps implement corrective action to maintain data compliance when necessary. Submits required “progress/tracking” reports to key stakeholders when applicable. Staff Training & Development Assists the CRM with recruitment and oversight of coordinator staff and ensures that staff have completed mandatory training in a timely manner. Helps implement program‑specific onboarding and orientation process and may participate in annual performance evaluations and competency assessments of research staff as needed. Knowledge, Skills, and Abilities Required Can 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. Has experience in protocol development, data compilation and analysis. Has a good understanding of the various tracking systems used to ensure timely data management by the clinical research staff. Understands Federal and State regulations as they relate to research; strong interpersonal, organizational and communication skills are required. Has computer skills including the use of Microsoft Office. Minimum Job Qualifications Bachelor’s Degree required. Minimum of 3 plus years of related experience preferred. Must have the ability to function independently, think critically and with good professional judgment. Supervisory Responsibilities No direct reports. Provides day‑to‑day supervision for study management staff, including clinical research coordinators, students, volunteers, and other research assistants as needed. Patient Contact May have contact with patients of all ages and populations. License/Certification/Registration N/A Pay Transparency Statement: 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). 70,000.00 – 85,300.00 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. #J-18808-Ljbffr Dana-Farber Cancer Institute