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Trial Document Specialist jobs - Newfoundland, NJ

Viewing 1 - 10 of 114 jobs

  • QA Specialist (Clinical Research)

    Memorial Sloan-kettering Cancer Center - New York City, NY

    Memorial Sloan Kettering Cancer Center is a world renowned organization dedicated to the progressive control and cure of cancer through programs of patient care, research, and education. Participate as a critical member of the Clinical...

    6 days ago from Memorial Sloan-Kettering Cancer Center

  • Grants Specialist 1021129 RR00000214

    Nyu Langone Medical Center - New York City, NY

    have an exciting opportunity to join our team as a Grants Specialist. To qualify you must have a Bachelor's degree plus proficiency in Microsoft Office, Word, Excel, Access and Internet applications. The successful candidate will be...

    7 days ago from NYU Langone Medical Center

  • Regulatory Documentation Specialist

    Maxisit - Woodcliff Lake, NJ

    obligations. · All types and aspects of ePublishing and document management. These types of publishing including, but ... R&D environment. · Solid knowledge of clinical trial transparency requirements, preferably on an international level ·...

    15 hours ago from Rekrutr.com

  • Regulatory Document Associate

    Tech Observer - East Hanover, NJ

    document updates/corrections; liaises with Field Monitor on trial documents and start up activities; liaises with ... a minimum of 1 year experience as a Regulatory Document Specialist or in Clinical Operations/Study Start-Up...

    1 day ago from Tech Fetch

  • Operations Specialist

    Oxford Solutions? - Whippany, NJ

    The Operations Specialist is responsible for all administrative aspects of investigational studies, company sponsored ... of clinical trials required. Experience in clinical trial management and operations in the pharmaceutical...

    11 days ago from ZipRecruiter

  • Regulatory Document Specialist Job Number: 14-00796

    Klein Management - East Hanover, NJ

    document updates/corrections; liaises with Field Monitor on trial documents and start up activities; liaises with ... a minimum of 1 year experience as a Regulatory Document Specialist or in Clinical Operations/Study Start-Up...

    19 days ago from ZipRecruiter

  • Regulatory Document Specialist

    Tech Observer - East Hanover, NJ

    Regulatory Document Specialist Position: Regulatory Documentation SpecialistDuration: 6 months (subject to ... document updates/corrections Liaises with Field Monitor on trial documents and start up activities Liaises with...

    20 days ago from Get Clinical Research Jobs

  • Medical Information Specialist

    Maxisit - Woodcliff Lake, NJ

    Job Description: The Medical Information Specialist is responsible for meeting the medical information needs of external ... information, clinical trial processes and drug approval processes. • Minimum of 1 year of experience in...

    30+ days ago from Rekrutr.com

  • Response Specialist

    Oxford Solutions? - Whippany, NJ

    type of follow up (HCP letter, consumer letter, Clinical Trial letter, etc) and assign to the appropriate individual ... critical follow-up information. Create and email Clinical Trial letters to the study sites to request follow up...

    12 days ago from ZipRecruiter

  • Paralegal Specialist

    Weill Cornell Medical College - New York City, NY

    ~~Position Summary Under supervision, provides litigation support in all phases of the litigation process and general legal assistance to attorneys in the Office of University Counsel. Position Activities · Creating and filing all court...

    14 days ago from ZipRecruiter

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