Clinical Research Manager I
Clinical Research Manager I
Boston Children's Hospital
Brookline, MA
See who Boston Children's Hospital has hired for this role
The Dana-Farber/Boston Children’s Cancer and Blood Disorders Center has exceptional research and clinical programs in non-malignant hematology. The clinical service in non-malignant hematology includes a busy inpatient consult service, and approximately 5000 ambulatory visits per year, including about 1500 new patients annually.
This Clinical Research Manager I Will Be Responsible For
- Oversight of their disease group’s clinical trial portfolio and all related regulatory, compliance and performance metrics requirements.
- Identify and manage operational, logistical, and regulatory challenges related to the conduct of clinical trials and acts as a leader in overseeing their resolution.
- Assist the principal investigator in developing the protocol budget, in collaboration with Research Administration and the Budget offices.
- Develops and oversees the implementation of best practice guidelines for conducting various clinical research protocols
- Collaborates and consults with investigators and their staff on the design, development, and conduct of clinical research studies
- Assists the principal investigator in preparing manuscripts for publication.
- Oversee the subject enrollment, protocol treatment and follow-up care processes for protocol patients.
- Leads design and development of data management and data monitoring tools and procedures and supervises data management staff and activities in compliance with GCP and program standards.
- Leads and manages the work of multiple clinical research projects. Serves as Clinical Research Study / Trial Manager for one or more large, clinical studies.
- Manages communication between study staff and internal and external stakeholders
- Assumes responsibility for essential document compliance for entire portfolio. Implements systems to monitor and ensure regulatory document collection and maintenance compliance.
- Assumes responsibilities for all clinical trial reporting requirements; safety event, annual approval, deviations etc. Implements systems to monitor portfolio compliance.
- Responsible for the recruitment and oversight of all the research staff. Ensure that all staff complete required mandatory and ongoing training in a timely manner. Develops and oversees a program specific on-boarding and orientation process and conducts annual performance evaluations and competency assessments of research staff.
- Ensures work is performed in conformance with established hospital, program, federal, and state policies and procedures.
- Bachelor's degree in STEM or Psychology, Master's degree preferred.
- 6 years' of relevant work experience or Master's degree and 4 years' relevant work experience.
- Analytical skills to gather and interpret data in which the information or problems are moderately complex to complex.
- Well-developed communication skills in order to provide critical information to patients, effectively deal with conflicting views or issues, and the ability to mediate fair solutions.
- Advanced writing skills.
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Seniority level
Entry level -
Employment type
Full-time -
Job function
Other -
Industries
Hospitals and Health Care, IT Services and IT Consulting, and Research Services
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