Human Subjects Research Coordinator I

University of Rochester

8d•$21 - $30

About The Position

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. This is a full-time position (40 hrs/wk) in Ob/Gyn to conduct clinical research study among pregnant women. In particular this individual will be responsible for recruitment and administrative responsibilities for one NIH funded study under the direction of the Principal Investigator. This individual will screen and recruit potential study candidates and perform interviews, data/specimen collection, chart reviews, and data entry. Must work well as part of a team, be able to complete project tasks independently as requested, be comfortable with a variety of databases, be detail-oriented, and at all times demonstrate the ability to interact in a professional and positive manner in both verbal and written communications.

Requirements

Bachelor's degree and 3 years’ experience in clinical research coordination; or an equivalent combination of education and experience.
Phlebotomy training and certification required.
Must be able to work occasional weekends and in late afternoons/early evenings on some weekdays.
This position requires the ability to work independently.
The candidate must possess strong organizational and interpersonal skills in order to communicate with subjects, team mates, and other hospital staff.
The applicant must be willing to develop the logistics of subject enrollment, be persistent and flexible in assuring on-going subject cooperation/compliance, be detail oriented, and possess excellent data collection skills.
Computer skills required.

Nice To Haves

Knowledge of Microsoft Office and Windows software preferred.
Experience with data entry or management preferred.
Clinical Research Coordinator Certification preferred.

Responsibilities

Engagement and monitoring of study subjects
Schedule and conduct study visits, consenting participants and explaining study protocols to ensure patient compliance.
Responsible for subject tracking, administering the study vitamin D on the first study day, drawing blood, processing biological sampling, ensuring form completion, and adherence to protocol.
Assist in developing protocol with PI, recruitment strategies, and monitors target enrollment numbers.
Inform Cornell study team when subjects complete study and need to be reimbursed.
Interface with PI at Cornell to update on enrollment status and any issues that arise during the study.
Study administration, participates in advertising material development, and coordination of study with PI.
Responsible for the day-to-day operations of the study and must use independent judgment.
Completes interviews and phone calls with subjects as required by protocol.
Completion of source documents: CRFs, follow up phone calls, and subject mailings.
Provide collection, labeling, and coordination of study specimens to be delivered to the core laboratory; ensure labeling is correct and coordinate sample shipments to Cornell.
Perform chart reviews and information abstraction/recording, phone communications with subjects, fax/mail as necessary as pertains to enrolled subjects at your site.
Perform data entry and integrity checks; enter data into web based database and respond to sponsor data queries as they arise.
Interface with study monitors to answer any questions and keep complete regulatory and subject documentation.
Coordinate with the PI, the sponsor, and the data monitors to ensure regulatory and other documents are complete and on time.
Attend team meetings and conference calls as needed.