University of Rochester

Healthcare

HumanSubjectResearchSpecialist

$0–0k Rochester, New York, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Human Subject Research Specialist at University of Rochester. Skills: Human subject research, Protocol coordination, Data management. Coordinate human subject research activities. Screen eligible subjects”

Industry & Context.

Healthcare

What They're Looking For.

Must Have

Bachelor's degree required, Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program required, Skill in completing assignments accurately and with attention to detail required, Understand and follow data integrity standards and processes required

Nice to Have

Experience implementing and supporting data management systems in a scientific, research context preferred, Prior experience as a phlebotomist preferred

What You'll Do.

Coordinate human subject research activities

Screen eligible subjects

Obtain subject consent

Maintain documentation according to protocol

Coordinate specimen collection and processing

Administer research surveys

Create research databases

Collect data from EMR and other sources

and study team members

Ensure research activities comply with policies

Initiate and conduct human subject research

Distribute study information to team members

Participate in human subject recruitment

Review databases for eligible patients

Develop recruitment strategies

Conduct telephone interviews

Conduct consent process

Compile data dictionary

Inspect data from electronic records

Enter data into electronic medium

Review data for accuracy and completeness

Compile reporting on data capture status

Ensure participant adherence to protocol

Coordinate with biobank

Maintain knowledge of federal

Maintain knowledge of SOPs and guidelines

How You'll Work.

Team & Collaboration

Coordinate with PI; Coordinate with biobank; Coordinate with laboratory technicians; Coordinate with study team members; Coordinate with stakeholders; Coordinate with lab members; Coordinate with clinical staff

Communication Scope

Describing progress; Describing challenges

Full Job Description

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. _**Job Location (Full Address):**_ 601 Elmwood Ave, Rochester, New York, United States of America, 14642 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400151 Urology M&D Work Shift: UR - Day (United States of America) Range: UR URG 106 H Compensation Range: $21.36 - $29.90 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ This role coordinates the human subject research activities outlined in research protocols in the Department of Urology to advance translational and clinical research mission of the Department of Urology . This includes screening for eligible subjects according to protocol inclusion/exclusion criteria, consenting subjects, maintaining all documentation according to protocol, SOP & regulatory requirements and coordinating collection/processing of specimens, administration of research surveys and creating and updating research databases (REDCap or other platform as specified in the protocol) via collecting data, including compilation, registration and submission, from the EMR and other sources as applicable. The role will coordinate with PI, biobank, laboratory technicians and any other study team members and/or stakeholders to carry all out parameters of research activities as specified in t

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