Jobs
>
Rochester

    Human Subject Research Spec I - Rochester, United States - University of Rochester

    Default job background
    Description
    Opening

    Part Time 32 hours Range URG 106 SON Staff/Research Programs

    Schedule

    8:30 AM-5 PM

    Responsibilities

    This position ends 02/28/2025


    GENERAL PURPOSE:


    Serves as a research coordinator of a NIH funded grant, UPSIDE Moms, that focuses on maternal behaviors, metabolic changes, and cardiometabolic risk after pregnancy.

    This study operates in conjunction with an ongoing NIH funded study UPSIDE (Understanding Pregnancy Signals and Infant Development) and will be tracking mothers through up to four years post-delivery.

    The coordinator is responsible for supporting senior research staff and faculty to reach recruitment and retention goals and to ensure successful conduct of all study activities.

    Assess subject eligibility, coordinate consents, and enroll research subjects for clinical study. Coordinate and conduct research subject visits involving outpatient study visits, home or virtual visits per protocol. Ensures compliance with study protocol, regulatory and institutional requirements/standards.


    RESPONSIBILITIES:

    • Ensure integrity of all study data collected. Enter data into databases. Assist team in extracting data needed for presentations and publications. Identify, make recommendations, and resolve data extraction issues. Complete QA projects as assigned.
    • Conduct study visits with enrolled mothers and infants/children, paying special attention to the specific requirements in each visit type. Track clinic visits of each participant to ensure complete data collection. Subject assessments will include physical measures, biospecimen collection, and questionnaire administration. Study visits may sometimes occur on evenings or conducted at subject's home.
    • Monitor and track completion and timely return of home activities. Process and track subject payments.
    • Biospecimen processing: Working independently, collect and process various biospecimens from study participants in a timely and methodical fashion. Track the processing and storage of biospecimens (including, but not limited to, blood, urine, and saliva). Sample collection may sometimes occur on evenings. Pulling samples for analyses.
    • Assess subject eligibility and coordinate consents and enroll research subjects for clinical study. Ensures compliance with regulatory and institutional requirements/standards.
    • Assist in Preparing and submitting regulatory documents for submission to RSRB, WIRB, ORPA, and Sponsor.
    Other duties as assigned


    QUALIFICATIONS:

    • Bachelor's degree required
    • Bachelor's degree with major course work in an appropriate health, psychology, social or technical field preferred
    • 1-year experience in human subject research required;
    * or equivalent combination of education and experience required


    • Previous experience with working with women and/or young children preferred.
    • Communication Skills, Microsoft Office (Word, Excel, PowerPoint), reliable transportation, flexibility to work evenings as needed
    • Phlebotomy, CCRC preferred


    The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion to advance the University's mission to Learn, Discover, Heal, Create - and Make the World Ever Better.

    In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, citizenship status, or any other status protected by law.

    This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.

    How To Apply

    All applicants must apply online.

    EOE Minorities/Females/Protected Veterans/Disabled

    Pay Range


    Pay Range:
    $ $29.29 Hourly

    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.



  • The University of Rochester Rochester, United States

    This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols. Under the ultimate responsibility of the Principal Investi Clinical Research, Clinical, ...


  • University of Rochester Rochester, United States

    GENERAL PURPOSE: · We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for older adults with cancer. The Senior Research Coordinator will play a pivotal role in the execution and managem ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 110 Surgery-Cancer Control · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · The Sr. Clinical Research Specialist position serves to support Dept. of Surgery Division of Supportive Care in Cancer trials at Wilmot Cancer Institut ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 110 Surgery-Cancer Control · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for o ...


  • The University of Rochester Rochester, United States

    The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ul Clinical Research, Clinical, ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 108 Cancer Center/Clin Trials Ofc · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinat ...


  • University of Rochester Rochester, United States

    GENERAL PURPOSE: · This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols. Under the ultimate responsibility of the Principal Investigator (PI) ...


  • The University of Rochester Rochester, United States

    We are seeking a highly motivated and experienced Senior Clinical Research Specialist to join our dynamic team focused on advancing health equity for older adults with cancer. The Senior Research Coordinator will play a pivotal role in the execution Clinical Research, Clinical, R ...


  • University of Rochester Rochester, United States

    GENERAL PURPOSE: · The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ultimate resp ...


  • University of Rochester Rochester, United States

    GENERAL PURPOSE: · The Sr. Clinical Research Specialist position serves to support Dept. of Surgery Division of Supportive Care in Cancer trials at Wilmot Cancer Institute. The coordinator will be responsible for leading the planning, implementation, and conduct of interventional ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 110 Surgery-Cancer Control · Schedule · 8 AM-4:30 PM · Responsibilities · GENERAL PURPOSE: · This position is an experienced Clinical Research Professional responsible for providing leadership in planning, implementing, monitoring, and evalu ...


  • The University of Rochester Rochester, United States

    Human Subject Research Spec I Next Job Apply for Job When you are ready to apply, registering only takes a minute. Your online account allows you to upload your resume or CV, apply for jobs and access our online career tools. For general questions ab Research, Technology, Educati ...


  • University of Rochester Rochester, United States

    Human Subject Research Spec I · Next Job · Apply for Job · When you are ready to apply, registering only takes a minute. Your online account allows you to upload your · resume or CV, apply for jobs and access our online career tools. · For · general questions about the online app ...


  • University of Rochester Rochester, United States

    GENERAL PURPOSE: · The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical trials within the URCC NCORP Research Base. The work performed requires a high degree of accuracy, the ability ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 106 Surgery-Cancer Control · Schedule · 8 AM-5 PM · Responsibilities · GENERAL PURPOSE: · The Data Control Clerk II is responsible for data entry and data management activities of large, multi-site biomedical and social-behavioral clinical t ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 106 Ortho, Clinical Research · Schedule · 8 AM-4:30 PM; OCC WKNDS · Responsibilities · GENERAL PURPOSE: · Coordinates the activities associated with human subject research. This person will be responsible for recruitment and have administrat ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 106 General Pediatrics · Position ends July 31, 2024 · Strong Candidate Identified · Position ends July 31, 2024 · Schedule · 11 AM - 2 PM; WKNDS; NO HOLIDAYS, EVENINGS AND WKNDS REQUIRED; SCHEDULE VARIES BASED ON OPERATIONAL NEEDS. · How To ...


  • University of Rochester Rochester, United States

    Responsibilities · **Position Summary** · This is a full-time position (40 hrs/wk) in Ob/Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the ...


  • The University of Rochester Rochester, United States

    This is a full-time position (40 hrs/wk) in Ob/ Gyn to conduct clinical research studies. In particular this individual will be responsible for recruitment and administrative responsibilities for several studies under the direction of the Principal I Clinical Research, Research, ...


  • University of Rochester Rochester, United States

    Opening · Full Time 40 hours Range URG 106 Peds Gastro/Hepatology/Nutrit · Schedule · 8 AM-4:30 PM · Responsibilities · GENERAL PURPOSE: · Coordinates the activities associated with human subject research. · JOB DUTIES AND RESPONSIBILITIES: · * Coordinates the administrative deta ...