Research Program Coordinator I - Sickle Cell Disease (CIBMTR)

Medical College of Wisconsin•Milwaukee, WI

8d•Onsite

About The Position

Work closely with the Center for International Blood and Marrow Transplant Research (CIBMTR) Senior Scientific Director, Protocol Team members, and other Research Coordinators and staff to coordinate the daily administrative activities for a new Sickle Cell Disease (SCD) study focused on long-term follow-up of individuals living with SCD who received either hematopoietic stem cell transplant or gene therapy. Provide support to the team to facilitate the achievement of the program's goals.

Requirements

Knowledge of computers, Microsoft Office, quantitative and (potentially) qualitative research methods, survey development, mathematics, documentation, and records management.
Organization, time management, interpersonal, communication, and problem-solving skills.
Bachelor's degree
2 years of experience

Nice To Haves

Experience working with individuals living with sickle cell disease or other chronic conditions
Demonstrated experience serving as a patient advocate or engaging with patient communities
Knowledge of the challenges faced by individuals and families affected by sickle cell disease
Experience with Sickle Cell Disease community (professional or volunteer)

Responsibilities

Organize and coordinate internal and external meetings, site visits, educational events, and other program-related activities.
Coordinate program outreach activities by serving as a liaison with community organizations, advocacy groups (such as Sickle Cell advocacy groups), and partner institutions.
Assist with planning and coordination of external engagement opportunities such as podcasts, webinars, and educational seminars.
Coordinate day-to-day program operations, maintain program timelines, and track milestones and deliverables to ensure timely completion of program activities.
Develop, maintain, and update program databases, participant records, and other program documentation to ensure data accuracy, organization, and regulatory compliance with institutional, regulatory and study requirements.
Coordinate research protocol activities by collaborating with partnering institutions, SCD clinical and treatment teams, and study personnel to support compliance and participant follow up.
Serve as a primary point of contact and patient advocate by facilitating communication between patients, physicians, researchers and CIBMTR.
Support participant recruitment, retention and engagement by addressing questions, providing study information, and promoting a positive research study experience.
Collaborate on the development, implementation and continuous improvement of educational, marketing, patient-facing, research, and training resources.
Support dissemination of findings through abstracts, manuscripts, and reports.
Collect, track, analyze, and report program and research data; prepare reports, dashboards, and updates for investigators, leadership, sponsors, and other stakeholders.
Coordinate and support training activities for program participants, clinical partners, research staff, and other stakeholders as appropriate.
Participate on internal committees and external workgroups that support program initiatives, organizational goals and professional development.
Perform other duties as assigned.

Benefits

Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental.
Flexible Spending options
403B Retirement Package
Competitive Vacation and Paid Holidays offered
Tuition Reimbursement
Paid Parental Leave
Employee & Family Assistance Program (EFAP)
Pet Insurance
On campus Fitness Facility, offering onsite classes
Additional discounted rates on items such as: Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.