Clinical Study Project Manager - Chicago, IL, United States - Shirley Ryan AbilityLab

Description

You'll work in a truly inclusive environment where diversity and equity are championed through words and actions.

You'll play a role in something that's never been done before as we integrate science and clinical care to help patients achieve better, faster outcomes — as we Advance Human Ability, together.

The Clinical Research Coordinator will coordinate the research component of the specified clinical program at the Shirley Ryan AbilityLab (SRAlab).

The Clinical Research Coordinator will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contributing to the team efforts and showing respect and compassion for patients and their families, fellow employees, and all others with whom there is contact at or in the interest of the institute.

The Clinical Research Coordinator will demonstrate Shirley Ryan Ability

Lab Core Attributes:

Communication, Accountability, Flexibility/Adaptability, Judgment/Problem Solving, Customer Service and Core Values (Hope, Compassion, Discovery, Collaboration, and Commitment to Excellence) while fulfilling job duties.

The Clinical Research Coordinator will:
Maintain clinical database including obtaining subject consent, extracting data from medical records and querying database.
Coordinate research projects including preparing and maintaining IRB documents, subject consents and grant budgets.
Perform statistical analysis on data for research purposes.
Assist in preparation of grant proposals, manuscripts for publication, scientific presentations and annual reports.
Serve on the research team, screening subjects for participation, performing physical examinations and coordinating with all involved departments.
Where required, collect study data and/or provide study intervention as required by study proposal.
Reports to the Medical Director, Principal Investigator, or Department Head of the program, as appropriate.

Minimum 1 year of experience in clinical research or doctoral prepared.
Written communication skills vital to this role, with experience in technical and medical writing preferred.

Normal office environment with little or no exposure to dust or extreme temperature.

All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.