What are the responsibilities and job description for the Project Manager BWH Cardiovascular position at Brigham & Women's Hospital(BWH)?
Project Manager BWH Cardiovascular
- (3282357)
Located within the Brigham and Women’s Hospital, the Cardiac Imaging Core Lab (CICL) is a nationally recognized academic research organization providing cardiac imaging core lab services for primarily large-scale international clinical trials for both industry and federal sponsors. The CICL’s primary throughput is quantitative imaging analysis data which is sent directly to the sponsor or CRO. There are thirty plus staff consisting of physician leadership, statisticians, cardiac imaging specialists and project management staff serving 30-40 ongoing clinical trials at any given point. The primary interface for the CICL is with sponsors, CROs, and clinical trial sites across the globe which send imaging studies directly to the CICL. Given the regulatory rigor with which research is conducted, the technical complexities of image analysis and associated systems, and the individual sponsor/CRO requirements, the CICL maintains close ties with MGB research compliance and information systems and security departments.
Within the CICL organization, this position serves as the CICL Project Manager, responsible for independently managing all aspects of CICL trials including image receipt and processing, data transfer, and reporting.
PRINCIPAL DUTIES AND RESPONSIBILITIES
Project Management:
- On a daily basis, provides clear and consistent organization of each assigned trial’s status with strong attention to detail; this includes hands-on tasks such as tracking media received, inventory control, ensuring proper follow-up of pending project tasks, monitoring project timelines and associated reporting of study-specific metrics to sponsors/CROs.
- Participates in all CICL related decisions made for the study.
- Ensure smooth and efficient internal day-to-day operations for numerous assigned studies. This will include serving as the primary liaison with Sponsor/CRO and CICL leadership for day-to-day issues, progress reporting, and attending study specific meetings.
- Represent the CICL as site Investigator Meetings and imaging-centered training sessions for site staff. Includes both development of training materials, tracking attendance, and presenting data about the CICL and applicable study.
- Responsible for the oversight of all study files.
- Maintain appropriate document control standards per MGB and CICL SOPs.
- Processing incoming patient/study documents and images for accuracy and completeness. Includes troubleshooting technical issues pertaining to images received including repairing image files and removing PHI from images and following associate PHI breach protocols.
- Providing site feedback for sonographer certification, eligibility confirmation and quality feedback. Includes working with sites to distribute and resolve CICL-generated queries.
- Assist technical teams with prioritizing timelines by creating project analysis lists and schedules.
- Reporting study metrics to Business Manager for invoicing purposes and other reporting as requested.
- Directly support site representatives with questions regarding study protocol, queries, and the image submission process. Respond and field questions submitted to the CICL site line and helpdesk email.
- Coordinate and monitor ongoing reproducibility assessments as a part of new hire training.
Information Systems:
- Serve as a liaison between CICL and MGB Information Systems/Information Security personnel for issues as they pertain to CICL computer systems, data security, software development, infrastructure improvement, quality improvement, and workstation issues.
- Serve as a liaison between external vendors for CICL software and analysis programs, including troubleshooting, software upgrades, and new software procurement.
- Support technical staff with software and workstation updates to ensure optimal workflow.
- Assist with database and software validation.
- Provide and monitor access to CICL secure file shares. Assist staff with mapping file shares.
Data Management:
- Creation of new, and management of existing CICL databases.
- Responsible for generating both study-specific progress reports and data as well as generating center-wide cumulative data and progress reports.
- Work with Study Sponsors and/or Data Coordinating Centers along with the CICL Clinical Data Coordinator to ensure proper data management, including data transfers of final data to study Sponsors.
General:
- Facilitate the implementation and ongoing process improvement of established CICL Policies and Procedures; responsible for monitoring the effectiveness and adherence to policies, generation of new policies, prn.
- Provide other support as per the CICL Directors as it relates to the overall research scope of the CICL.
- Train and assist with onboarding CICL Operational and Technical Team members.
- Attend CICL Operational and Team meetings, providing necessary updates.
- Provide back-up coverage for CICL Operational Team as needed.
- BA/BS degree in biological sciences or health administration.
- Research professional with at least 5 years’ experience in clinical research and/or trial project management.
- Knowledge of FDA regulations, ICH and GCP guidelines concerning human subject research especially as they relate to computer systems/security, disaster recovery and regulatory compliance of research core labs.
SKILLS/COMPETENCIES REQUIRED
Given this is a project environment and multiple projects will be assigned, and given that each project will have unique project demands, staff, deliverables and timeline, the ideal candidate is:
- highly organized and systematic in work processes
- self-motivated and proactive; able to identify, track, and drive issue resolution with little or no supervision or prompting
- able to function at a high level in a dynamic and busy environment
- able to take direction from, as well as influence and establish strong working relationships with a wide variety of individuals at all levels; ie. other Center project staff, technical staff, Directors, enrolling sites, Sponsors and other affiliate groups
- very dependable and able to demonstrate a respect for the importance of how work practices affect data quality
- able to communicate concisely and effectively, without undue delays, both verbally and in writing
- a clinical research professional, or aspires to become one, with an interest in cardiovascular medicine, human subject research and clinical trial project management.
SUPERVISORY RESPONSIBILITIES
None.
WORKING CONDITIONS
The CICL supports a hybrid work model. This position is M-F during core business hours.
BWH is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
Primary Location MA-Boston-BWH Boston Main Campus
Work Locations BWH Boston Main Campus 75 Francis St Boston 02115
Job Research-Management
Organization Brigham & Women's Hospital(BWH)
Schedule Full-time
Standard Hours 40
Shift Day Job
Employee Status Regular
Recruiting Department BWH Department Of Medicine / Cardiovascular Medicine
Job Posting Mar 19, 2024
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