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  • Brigham & Women's Hospital(BWH)

    Program Director BWH Cardiovascular

    Boston, MA, United States

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    Job Source: Brigham & Women's Hospital(BWH)
  • Brigham & Women's Hospital(BWH)

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    Job Source: Brigham & Women's Hospital(BWH)
  • Brigham and Women’s Hospital

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    Job Source: Brigham and Women’s Hospital
  • Brigham & Women's Hospital(BWH)

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    Job Source: Brigham & Women's Hospital(BWH)
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  • Brigham and Women’s Hospital

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    Job Source: Brigham and Women’s Hospital
  • Brigham and Women’s Hospital

    Echo Specialist Per Diem BWH Cardiovascular

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  • Brigham & Women's Hospital(BWH)

    Clinical Trial Coordinator BWH Cardiovascular

    Boston, MA, United States

    Day-to-Day Study Operation One of the day to day responsibilities for this role is to provide daily administrative support to the Director. Provide 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 follo

    Job Source: Brigham & Women's Hospital(BWH)

Program Director BWH Cardiovascular

Boston, MA, United States

Job Description - Program Director BWH Cardiovascular (3292851)

Program Director BWH Cardiovascular - ( 3292851 )

The Cardiac Imaging Core Lab (CICL) is an academic research organization located within the Brigham and Women’s Hospital, a Harvard-affiliated hospital. The CICL provides echocardiography core laboratory services for primarily large-scale global clinical trials responsible for site training and interface as well as echo analysis of images received. There are approximately 40 staff supporting 40+ clinical trials ongoing at any given time with a typical volume of 1000 – 1500 echos received each month. Reporting to CICL Faculty Directors, the CICL is recruiting a Program Director to advance its technical and operational directives.

The Program Director will work directly with CICL faculty and CICL’s Technical, IT, and Operational Directors to advance the mission of the CICL. The Program Director will be responsible for strategic planning and process improvements of the CICL’s research services, coalescing sponsor requirements, internal resources, technical capacity, and IT/system constraints. They will serve a highly visible central role to drive progress and execute services within the CICL portfolio. In addition to helping to conceive strategic initiatives, they will set priority to support operational and technical direction of the Center. This position requires superior skills in project management, analytics, and communication.

PRINCIPAL RESPONSIBILITIES:

Strategic Visioning: Collaborate with Directors to lead strategic planning, program development, and process improvement, ensuring technical and administrative staff and operations are maximized for efficiency. Oversee project logistics and communication (e.g., meeting agendas, action logs, slide decks) to ensure activities are tracked and are consistent with plans. Provide and cultivate effective meeting management skills and participation. Uses critical thinking skills to independently manage high-priority, complex initiatives that support CICL strategic priorities.

Expert Problem-Solving: Provide logistical expertise and innovative solutions to complex technical and operational challenges. Develop detailed project plans that are practical and of appropriate scope, and includes identification of stakeholders, assessment of resource needs, and implementation timelines. Propose modifications to technical and administrative resource allocations to improve workflow.

Goal Execution & Monitoring: Ensure timely realization of study-specific and lab-wide objectives. Create new and develop existing reports that provide visibility and monitoring of ongoing CICL initiatives. Analyze technical throughput across all studies to evaluate performance and identify improvement opportunities.

Stakeholder Engagement: Keep senior faculty, technical and operational staff aware of ongoing issues, working to provide greater transparency between teams. Rapidly identifies, problem solves, and communicates any issues that are jeopardizing effectiveness of CICL initiatives. Independently facilitates project subgroups and work teams including meeting management, discussion facilitation, conflict resolution, change management, and one-on-one meetings with technical and administrative managers and leaders. Liaise with sponsors and industry partners when needed.

Team Development: Help identify areas within CICL that require staff resource adjustments to maximize technical and operational efficiency. Foster a collaborative work environment that emphasizes teamwork and engagement. Maintain strong and productive relationships with key stakeholders.

Operational Excellence: Trigger further development of SOPs and systems to further comply with current regulations and meet evolving needs of the CICL. Interact extensively with all functional leads to revise SOPs and other internal documentation practices in keeping with strategic improvement initiatives.

Adaptable Leadership: Take on other strategic and operational tasks as the Center grows and evolves. This team member will need to demonstrate flexibility and open-mindedness as the contours of this position will actively evolve over time.

Other duties as assigned.

Minimum of 7-10 years directly related experience

Minimum of 2 years of supervisory experience required

Understanding and working knowledge of principles of SOPs, GCP, FDA, IRB, clinical research methodology, regulations, and compliance required

SKILLS/COMPETENCIES REQUIRED:

Planning, Organizing and Coordinating

Skilled in identifying and implementing opportunities to improve efficiency of research operations and subsequently execute improvements

Time management skills with the capability to prioritize among multiple requests from multiple individuals with the ability to change direction in response to a fluctuating work environment

Ability to delegate, prioritize, and assist others with prioritizing study tasks

Team Management

Ability to work successfully in a collaborative environment

Ability to manage diverse teams with different skillsets, work styles, and professional roles

Gets Results/Takes Initiative

High personal work standards and sense of urgency about results

Ability to anticipate the needs of the group in a fast-paced environment

Problem-solving ability, including the ability to analyze complex situations, identify resources, and imagine alternatives

Demonstrates initiative and identifies key priorities, even in ambiguous situations with limited direction

Ability to work effectively under pressure and within short time constraints

Consistently demonstrates a positive, "can-do" attitude

Communication Skills

Excellent written and verbal communication skills

Ability to represent the program with the utmost professionalism and ability to build strong relationships inside and outside the group

Ability to clarify and distill complex issues to a variety of stakeholders

Demonstrated ability to lead discussions/meetings, and obtain cooperation and support from team

Cognizant and respectful of cultural differences in communication approach

Analytical Skills

Intellectual curiosity and willingness to learn

Rigorous academic and/or professional background including healthcare work

Extensive familiarity with clinical research

This description has been designed to indicate the general nature and level of work performed by an employee within this position. The actual duties, responsibilities and qualifications may vary based on need.

SUPERVISORY RESPONSIBILITIES:

As position of authority within the CICL, this position will have a role in monitoring the efficiency of its technical and operational support staff and advocating for necessary changes to CICL Director.

WORKING CONDITIONS:

The CICL supports a hybrid work model. This position is M-F during core business hours. There is no patient interaction in this position.

BA/BS, Master’s degree preferred

Minimum of 7-10 years directly related experience

Minimum of 2 years of supervisory experience required

Understanding and working knowledge of principles of SOPs, GCP, FDA, IRB, clinical research methodology, regulations, and compliance required

SKILLS/COMPETENCIES REQUIRED:

Planning, Organizing and Coordinating

Skilled in identifying and implementing opportunities to improve efficiency of research operations and subsequently execute improvements

Time management skills with the capability to prioritize among multiple requests from multiple individuals with the ability to change direction in response to a fluctuating work environment

Ability to delegate, prioritize, and assist others with prioritizing study tasks

Team Management

Ability to work successfully in a collaborative environment

Ability to manage diverse teams with different skillsets, work styles, and professional roles

Gets Results/Takes Initiative

High personal work standards and sense of urgency about results

Ability to anticipate the needs of the group in a fast-paced environment

Problem-solving ability, including the ability to analyze complex situations, identify resources, and imagine alternatives

Demonstrates initiative and identifies key priorities, even in ambiguous situations with limited direction

Ability to work effectively under pressure and within short time constraints

Consistently demonstrates a positive, "can-do" attitude

Communication Skills

Excellent written and verbal communication skills

Ability to represent the program with the utmost professionalism and ability to build strong relationships inside and outside the group

Ability to clarify and distill complex issues to a variety of stakeholders

Demonstrated ability to lead discussions/meetings, and obtain cooperation and support from team

Cognizant and respectful of cultural differences in communication approach

Analytical Skills

Intellectual curiosity and willingness to learn

Rigorous academic and/or professional background including healthcare work

Extensive familiarity with clinical research

This description has been designed to indicate the general nature and level of work performed by an employee within this position. The actual duties, responsibilities and qualifications may vary based on need.

SUPERVISORY RESPONSIBILITIES:

As position of authority within the CICL, this position will have a role in monitoring the efficiency of its technical and operational support staff and advocating for necessary changes to CICL Director.

WORKING CONDITIONS:

The CICL supports a hybrid work model. This position is M-F during core business hours. There is no patient interaction in this position.

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 Work Locations 75 Francis St

Job Job Professional/Managerial

Organization Organization Brigham & Women's Hospital(BWH)

Schedule Schedule Full-time

Standard Hours 40

Shift Shift Day Job

Employee Status Employee Status Regular

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