Clinical Trials Proj Spec I A

3 weeks ago

Rochester, United States University of Rochester Full time

Opening

Full Time 40 hours Range URG 108 Neuro-Ctr Health & Tech/CTCC

Schedule

8 AM-5 PM

Responsibilities

GENERAL PURPOSE:

The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory documents from study sites and maintaining study files. Individuals assist more senior Clinical Project Coordinators in supporting clinical trial sites. Responsible for helping prepare for various clinical study meetings involving both internal and external teams.

JOB DUTIES AND RESPONSIBILITIES:

* Under direction of study team leader, requests, tracks receipt of and reviews regulatory documents and IRB approved documents received from clinical study sites. Requests and tracks updated documents when necessary. Reviews site informed consents and may advise sites on revisions based on the model consent under the direction of the study team lead. Files correspondence pertaining to the review and approval process in site file.
* Maintains a central file and tracking of professional licenses, human subject protection training and good clinical practice training certification for all active site personnel.
* Assists more senior project managers in preparing for meetings by helping to schedule meetings, manage meeting invitations, open calls and webinars, prepare agendas and distribute materials.
* Demonstrates ability to monitor site IRB expirations and request current approvals as necessary. Utilizes internal tracking system to monitor upcoming IRB expirations and contacts sites to obtain renewals.
* Under direction of study team leader, processes requests for information and documentation from functional groups (e.g., Data Management and Biostatistics) and compiles information in report-ready format.
* Assists with file archiving of clinical study specific files in a centralized archive to ensure secure storage and retrieval for the custody of study documents.

Other duties as assigned.

QUALIFICATIONS:

Bachelor's degree required with major course works in appropriate health, social science, or biological science field or equivalent combination of education and experience. Some clinical trials experience preferred. Knowledge of Good Clinical Practice, protocol planning, implementation, coordination, evaluation, and reporting of clinical trials preferred. Strong verbal and written communication skills, interpersonal skills, attention to detail and organization required.

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: $24.40 - $34.16 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.

  • Clinical Trials Proj Spec I A

    1 month ago

    Rochester, United States The University of Rochester Full time

    The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education

  • Clinical Trials Proj Spec I A

    4 days ago

    Rochester, New York, United States The University of Rochester Full time

    The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the c Clinical, Clinical Research, Project Coordinator, Team Leader, Healthcare, Education

  • Clinical Trials Proj Spec I A

    4 weeks ago

    Rochester, United States University of Rochester Full time

    GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...

  • Clinical Trials Proj Spec I A

    3 weeks ago

    Rochester, United States University of Rochester Full time

    GENERAL PURPOSE: The responsibility of the Clinical Project Coordinator I is to help coordinate all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment. The Clinical Project Coordinator I supports the clinical study team by assisting with collection and tracking of study related regulatory...

  • Clinical Trials Proj Spec I A

    3 weeks ago

    Rochester, United States The University of Rochester Full time

    With direction from the Clinical Research Manager, assists with coordination of clinical research management activities for large international multi-site studies within the Clinical Cardiology Research Center to be consistent with Good Clinical Prac Clinical, Clinical Research, Healthcare, Media, Training, Electronic

  • Clinical Trials Proj Mgr II

    2 months ago

    Rochester, United States The University of Rochester Full time

    The Clinical Research Project Manager (CRPM) position involves working with multiple principal investigators across multiple clinical trials with a wide variety of assessment methods including patient-reported, biological, physiological, and electron Clinical, Clinical Research, Project Management, Equipment, Auditor, Exercise, Education

  • Clinical Trials Lead Proj Mgr

    2 months ago

    Rochester, United States The University of Rochester Full time

    The Clinical Project Lead directs and coordinates all aspects of multi-center international clinical research trials in a Contract Research Organization (CRO) environment and acts as a liaison to study leadership and sponsor(s). Individual ensures st Clinical, Clinical Research, Project Management, Project Coordinator, Project Lead, Lead, Business Services

  • Clinical Research Data Spec I

    2 months ago

    Rochester, United States The University of Rochester Full time

    Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating proced Clinical Research, Clinical, Research, Data, Monitoring, Management, Technology

  • Clinical Research Data Spec I

    4 weeks ago

    Rochester, United States University of Rochester Full time

    Opening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...

  • Clinical Research Data Spec I

    4 weeks ago

    Rochester, United States University of Rochester Full time

    GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...

  • Clinical Research Data Spec I

    3 weeks ago

    Rochester, United States University of Rochester Full time

    GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Under supervision from these senior level staff, coordinates with the investigational...

  • Clinical Research Data Spec I

    3 weeks ago

    Rochester, United States University of Rochester Full time

    Opening Full Time 40 hours Range URG 106 Neuro-Ctr Health & Tech/CTCC Schedule 8 AM-5 PM Responsibilities GENERAL PURPOSE: Under the direction of the senior staff of the assigned clinical trial, assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department...

  • Clinical Trials Proj Mgr II

    2 months ago

    Rochester, United States The University of Rochester Full time

    This position requires working with cancer patients and survivors at Wilmot Cancer Institute locations by managing all research activities for Re. NEW within the PEAK Human Performance Science Program; a clinical and implementation exercise oncology Clinical, Clinical Research, Exercise, Healthcare, Education, Development, Oncology, Patient

  • Human Subject Research Spec I

    2 months ago

    Rochester, United States The University of Rochester Full time

    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, Education

  • Clinical Research Data Spec I

    4 weeks ago

    Rochester, United States University of Rochester Full time

    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 to exercise some independent judgment, flexibility to vary specific tasks as...

  • Clinical Research Data Spec I

    4 weeks ago

    Rochester, United States University of Rochester Full time

    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 trials within the URCC NCORP Research Base. The work performed requires a high degree...

  • Clinical Research Data Spec I

    2 weeks ago

    Rochester, United States University of Rochester Full time

    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 to exercise some independent judgment, flexibility to vary specific tasks as...

  • Clinical Research Data Spec I

    3 weeks ago

    Rochester, United States University of Rochester Full time

    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 trials within the URCC NCORP Research Base. The work performed requires a high degree...

  • Med Technologist-Spec

    2 months ago

    Rochester, United States The University of Rochester Full time

    The Med Technologist-Spec is responsible for the timely and accurate reporting of results, maintenance and troubleshooting of laboratory instrumentation, development of new procedures and instruments, writing/updating of procedure manuals, training o Med Tech, Technologist, Clinical, Chemistry, Laboratory, Technical, Healthcare

  • Clinical Laboratory Technologist

    2 months ago

    Rochester, United States Mayo Clinic Full time

    This position is available only to those currently in a Contractor position in the Clinical Mass Spec Lab Performs analyses on blood, tissue, and body fluids to aid health care providers in the diagnosis, prognosis, and treatment of patients. Participates in the operational support activities necessary to maintain and optimize testing capabilities....