- Merck & Co. (North Wales, PA)
- …or work quality - Building expertise in the regulations associated with clinical trial PLS and adapting to the changing regulatory environment as needed - - ... : - Authoring accurate , clear and health literate clinical trial PLS for posting on EU...and communities - Background in medical writing, authoring ICH clinical / regulatory documents (ie, Informed Consents, Clinical… more
- Eisai, Inc (San Diego, CA)
- …state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory /compliance guidelines.Strong ... want to hear from you. Job Summary The Sr. Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic products… more
- Eisai, Inc (Louisville, KY)
- …state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory /compliance guidelines.Strong ... want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …inspection/release of materials related to manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP ... of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom ... in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role… more
- DivIHN Integration Inc (Atlanta, GA)
- …manner. Strong organizational skills and meticulous attention to detail. Familiarity with clinical trial -related and regulatory clinical submission ... inquiries regarding the following opportunity, please contact our Talent Specialist Divya at 224 369 2969 Title: Senior Medical...5 years of on-the-job experience in scientific/medical writing (eg, clinical trial and regulatory documents)… more
- University of Pennsylvania (Philadelphia, PA)
- …as assigned. Job Description + Clinical Research Regulatory Affairs Specialist A Assist in Clinical Trial proposal submissions. Provides day-to-day ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist A...provide regulatory support and expertise associated with clinical trials . The person will support a… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The...-CC to participate in the coordination of Phase I-V clinical trials . Reporting to the Regulatory… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …can contribute to the diversity and excellence of our academic community. **Description** The Clinical Trials Regulatory Specialist I is an entry-level ... position supporting regulatory affairs in clinical trial research. The primary focus of...small trial portfolio. KEY RESPONSIBILITIES: + Assists regulatory team ( Regulatory Specialist II… more
- University of Southern California (Los Angeles, CA)
- … SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research- Regulatory - Specialist ... information pertinent to studying milestone progress, including but not limited to: clinical trial management systems, IRB databases, internal and external… more
- Vanderbilt University Medical Center (Nashville, TN)
- …in patient care, education, and research. **Organization:** VICTR **Job Summary:** Associate Clinical Research Regulatory Affairs Specialist - VICTR - ... departments to deliver safe and effective research designs for clinical trials in line with institutional policies...In 2016, with the addition of several large, innovative clinical trial grants within the Vanderbilt Institute… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and...CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The Clinical Research Regulatory Support Specialist II is responsible, for the coordination and oversight of regulatory requirements of ... Principal Investigator (PI) and other study team members, the Clinical Research Regulatory Support Specialist ...they relate to on-site and other site(s) participation in clinical trials and affiliate participation. + Prepares,… more
- Sumitomo Pharma (Columbus, OH)
- …conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables, ... highly motivated, and experienced individual for the position of ** Clinical Trail Associate.** The Clinical Trial...electronic TMF systems (ie, Veeva) + Will assist/back-up the Clinical Regulatory Operations Specialist for… more
- Dana-Farber Cancer Institute (Boston, MA)
- …not limited to e- Regulatory Management and the IND and IDE databases. ** CLINICAL TRIAL OPERATIONS** + Problem-solves with or advises investigators and study ... The Regulatory Affairs Specialist (RAS) positions provides...acceptability of regulatory documentation to comply with regulatory requirements for clinical trials .… more
- Georgetown Univerisity (Washington, DC)
- …Diseases Clinical Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial ... patient specimens, processing the specimens, and entering data into clinical trial sponsor system. The incumbent will...a clinical research perspective. + Partner with clinical staff to help with the regulatory … more
- Houston Methodist (Houston, TX)
- …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... and study specific protocols/plans and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case… more
- Hackensack Meridian Health (Edison, NJ)
- …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant… more
- Stryker (Fremont, CA)
- …Stryker Neurovascular is seeking a ** Clinical Trial Specialist ... prevent future issues. **What you will do** As the ** Clinical Trial Specialist (Hybrid)** ,...study according to the clinical protocol, "Good Clinical Practices", and regulatory requirements + Ensure… more
- Actalent (New Brunswick, NJ)
- Job Title: Clinical Trial Specialist + As a Clinical Trial Specialist , you will be integral to the initiation, activation, and ongoing management ... of clinical trials . + You will collaborate with...and performance, while staying current with continuing education and regulatory requirements. Hard Skills + 2-3 years clinical… more
