• Team Lead, Clinical Trials

    Rochester Regional Health (Rochester, NY)
    Job Title: Team Lead, Clinical Trials Specimen Management Department: Specimen Processing Location: Rochester, NY Hours Per Week: 40 Schedule: ... Tuesday - Saturday; 8:00AM - 4:30PM SUMMARY The Clinical Trials Specimen Management Team Lead supports the supervisor in overseeing, directing and… more
    Rochester Regional Health (07/01/25)
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  • Clinical Trials Specimen

    Rochester Regional Health (Rochester, NY)
    Job Title: Clinical Trials Specimen Management Technician Department: Specimen Processing Location: Rochester, NY Hours Per Week: 40 Schedule: ... Tuesday - Saturday; 8:00AM - 4:30PM SUMMARY The Clinical Trials Specimen Management Technician I performs the daily operations of specified area within… more
    Rochester Regional Health (07/01/25)
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  • Supervisor, Clinical Trials

    Rochester Regional Health (Rochester, NY)
    Job Title: Supervisor, Clinical Trials Specimen Management Department: Specimen Processing Location: Rochester, NY Hours Per Week: 40 Schedule: ... Tuesday - Saturday; 8:00 AM - 4:30 PM SUMMARY The Supervisor, Clinical Trials Specimen Management (CTSM) supervises a team dedicated to the timely… more
    Rochester Regional Health (04/26/25)
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  • Clinical Trial Specialist

    Caris Life Sciences (Phoenix, AZ)
    …bigger than yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist provides operational and regulatory support for the ... chain of custody, and routes for fulfillment. + Enters specimen information into Sample Management System. +...have 1-2 years' experience in a Biorepository setting or Clinical Trial setting. + Experience in handling… more
    Caris Life Sciences (07/09/25)
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  • Cancer Clinical Trials Assistant

    Stony Brook University (Stony Brook, NY)
    Cancer Clinical Trials Assistant **Required Qualifications (as evidenced by an attached resume):** High School Diploma/GED. A certificate in Phlebotomy from a ... Google Apps, etc.). **Preferred Qualifications:** Oncology and/or chemotherapy experience. Clinical trials research experience. IRB research training. **Brief… more
    Stony Brook University (06/05/25)
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  • Associate Director, Specimen Data & Systems

    Bristol Myers Squibb (Princeton, NJ)
    …experience in clinical drug development. + Expertise in biospecimen management and specimen meta-data standards. Exposure to biomarkers, pharmacokinetics ... meta-data and drive development and utilization of the BMS Specimen Management System (SMS) . + Act...perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of… more
    Bristol Myers Squibb (07/07/25)
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  • Research Data Specialist - Gynecologic Oncology…

    Dana-Farber Cancer Institute (Boston, MA)
    …patient status. The Research Data Specialist will be responsible for the collection, management , and quality assurance review of patient clinical data. **This ... Ensure case management documentation in patient medical records and other information management systems as assigned to support clinical program clinical more
    Dana-Farber Cancer Institute (05/29/25)
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  • Clinical Research Coordinator B/C (Abramson…

    University of Pennsylvania (Philadelphia, PA)
    …Obtain records required to complete case report forms. Update/maintain study record in the Clinical Trials Management System (CTMS) in real-time. Maintain ... training. The CRC is also responsible for research lab specimen processing/handling. The CRC will demonstrate vigilance in patient...for trials as needed. May support a clinical trial budget through each phase of… more
    University of Pennsylvania (05/04/25)
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  • Clinical Research Coordinator B/C…

    University of Pennsylvania (Philadelphia, PA)
    …The Clinical Research Coordinator B/C will assist in the coordination and management of multiple clinical trials along with other research projects ... collections from clinical labs) and transport/shipment of specimen samples, preparing trials for audits and...accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and… more
    University of Pennsylvania (05/17/25)
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  • Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …wide range of complex dermatology studies, including both investigator-initiated and industry-sponsored clinical trials . The CRC will report directly to the ... CRC will be integral to the smooth functioning of clinical trials , ensuring compliance with institutional, FDA,...accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and… more
    University of Pennsylvania (05/04/25)
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  • Clinical Program Manager (RN/NP Required)…

    Mount Sinai Health System (New York, NY)
    Clinical Trials Office (TCI CCTO). In collaboration with the disease management team, clinical trials investigators, and TCI CCTO Administration; this ... candidate is responsible for the implementation and conduct of clinical trials with investigational anti-cancer agents in the Cancer Institute. The Candidate… more
    Mount Sinai Health System (06/25/25)
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  • Clinical Research Coordinator B/C (Division…

    University of Pennsylvania (Philadelphia, PA)
    …Coordinator. The Clinical Research Coordinator will assist in the coordination and management of multiple clinical trials , along with other research ... Research Coordinator will assist in the coordination and management of multiple clinical trials ...collections from clinical labs) and transport/shipment of specimen samples, preparing trials for audits and… more
    University of Pennsylvania (05/06/25)
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  • Clinical Laboratory Scientist

    Veterans Affairs, Veterans Health Administration (Fayetteville, NC)
    Summary The incumbent serves as a Clinical Laboratory Scientist for the Pathology and Laboratory Medicine Service (Path & Lab) at the Fayetteville VA Medical Center ... human specimens for diagnosis, treatment, or prevention of disease in clinical laboratory specialties including, but not limited to, Hematology, Chemistry,… more
    Veterans Affairs, Veterans Health Administration (07/04/25)
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  • Clinical Research Coord Intermediate

    University of Michigan (Ann Arbor, MI)
    …first day + 2:1 Match on retirement savings **Responsibilities This role will include clinical trial management of Industry and NIH Sponsored Clinical ... biological specimen + A background in financial management such as Unfunded Agreements (UFAs), Clinical Trial Site Agreements (CTAs), and budget creation… more
    University of Michigan (06/21/25)
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  • Clinical Research Nurse II - Oncology

    BayCare Health System (Tampa, FL)
    …state regulations and institutional review board (IRB) requirements. + Lead and implement clinical trials under the direction of the Principle Investigator in ... that's built on a foundation of trust, dignity, respect, responsibility, and clinical excellence. **Title:** Clinical Research Nurse II - Oncology **Facility:**… more
    BayCare Health System (05/28/25)
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  • Clinical Research Nurse I (RN) - Oncology

    UPMC (Pittsburgh, PA)
    trials include institutional (investigator-initiated), multi-center cooperative group/National Clinical Trial Network (NCTN), consortium, and ... trials . Using a disease-specific centers model for conducting clinical trials , CRS provides study development and implementation assistance,… more
    UPMC (07/08/25)
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  • Clinical Research Coord Assoc

    University of Michigan (Ann Arbor, MI)
    …initiation meetings, monitor visits, and audits; Ensures integrity of specimen management (collection, processing, packing/shipping, storing, labeling, tracking, ... meetings, monitor visits, and audits. + Ensures integrity of specimen management (collection, processing, packing/shipping, storing, labeling, tracking,… more
    University of Michigan (07/01/25)
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  • Clin Research Nurse Coord

    Covenant Health Inc. (Knoxville, TN)
    …Coordinator promotes good clinical practices in the conduct of oncology clinical trials by possessing in-depth knowledge of federal regulations and guiding ... documents for the conduct of clinical trials and human participant protection. In...implements pre-study activities by developing timelines for conducting the clinical trial protocol, attending and participating in… more
    Covenant Health Inc. (06/03/25)
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  • Senior Clinical Data Manager

    GRAIL (Menlo Park, CA)
    …medical device and/or pharmaceutical industry. + Prior experience leading mid to large scale clinical trials and ability to support multiple projects at a given ... For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead data management...is maintained throughout the data lifecycle for sources including clinical data, external bio- specimen storage data, and… more
    GRAIL (05/14/25)
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  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    …enroll patients onto clinical trials in collaboration with clinical team, ensure protocol compliance; coordination of specimen collection and transmittal ... Overview Responsible for pre- clinical trial set up, initial and...regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management more
    Touro University (04/25/25)
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