- Merck & Co. (Rahway, NJ)
- …teamsThe Vocabulary Specialist maintains knowledge of new technologies, clinical study data standards, regulatory requirements emerging in industry, ... team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …business, and other functional groups across NN. External relationships can include clinical trial sites and external vendors. Essential Functions Develop and ... About the Department The Clinical , Medical and Regulatory (CMR) department...or resolve, for example across various topics, such as clinical trial management, deviation handling, and product… more
- Catalent (Manassas, VA)
- …health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion ... to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality… 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 Overview The… more
- Northeast Georgia Health System, Inc (Gainesville, GA)
- …of improving the health of our communities. About the Role:Job SummaryThe Research Regulatory Specialist performs a wide range of tasks essential to the ... submission, approval, and maintenance of required regulatory documents for conducting clinical research in...of high quality research within the department. Familiarity with clinical trials operations, finance, budgets, contracting and… more
- Integrated Resources, Inc (Cambridge, MA)
- Job Title: Senior Drug Safety Specialist Location: Cambridge, MA Duration: 8+ Months Job Description: Duties: . Reporting to the Associate Director, Drug Safety and ... role in drug safety activities, supporting records management and compliance across the clinical development and marketing programs. You will be a key contributor to… more
- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist **School of Medicine, Stanford, California, United States** Research Post Date Mar 27, 2024 Requisition # 102688 ... to effect positive changes in patient care. The PACCM is seeking a full-time Clinical Trials Regulatory Specialist (CTRS) to join our expanding … more
- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist 2 **School of Medicine, Stanford, California, United States** Research Post Date Feb 16, 2024 Requisition # 100464 ... innovative clinical research to improve human health. SCCR seeks a mission-driven Clinical Trials Regulatory Specialist 2. You will work with a… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …the diversity and excellence of our academic community. **Description** JOB DESCRIPTION: + The Clinical Trials Regulatory Specialist I is an entry-level ... position supporting regulatory affairs in clinical trial research. + The primary focus... trial portfolio. + Duties include: + Assists regulatory team ( Regulatory Specialist II… more
- Emory Healthcare/Emory University (Decatur, GA)
- …The Regulatory Specialist II is an intermediate level position supporting regulatory affairs in clinical trial research. + Incumbents are responsible ... reports. + Establishes and maintains processes and monitors practices to ensure regulatory documentation involving clinical trials complies with… more
- Methodist Health System (Dallas, TX)
- … clinical , investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, ... requirements * Obtain and facilitate tracking of relevant regulatory documents for clinical trials ...trials assigned. * Assist in the development of clinical trial documents for signature of principal… 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
- Houston Methodist (Houston, TX)
- …study specific protocols/plans and processes. The Sr Regulatory Compliance Specialist position maintains documentation for clinical research studies, case ... At Houston Methodist, the Senior (Sr.) Regulatory Compliance Specialist position is responsible...from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research… more
- Merck (West Point, PA)
- …of our pipeline and existing products to produce safe, effective, innovative medicine. The Clinical Trial Specialist partners with the early development ... extend and improve the lives of patients worldwide. Through clinical trials , we ensure the safety and...regulatory requirements + Knowledge of drug development and clinical trial processes, including related standards and… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Senior Associate Director, Clinical Trial Diversity supports the Clinical Development & Operations (CD&O) strategy for Diversity & ... Inclusion in clinical trials , focusing on the US. They...the development and execution of Diversity & Inclusion in clinical trial strategies, core processes and best… more
- Vitalief (New Brunswick, NJ)
- …activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high enrollment, ... Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: +… more
- UCLA Health (Santa Monica, CA)
- Description The Division of Hematology-Oncology is seeking an experienced Senior Clinical Trial Specialist to join our team. In this role you will be ... the liaison for the site management and monitoring of clinical trials in Santa Monica. Responsible for...conduct Site Initiation Visits and Interim Monitoring Visits with clinical trial sponsor representatives; you will also… more
- University of Pennsylvania (Philadelphia, PA)
- …Prepare any necessary regulatory documentation DUTIES: The Clinical Trials , Billing, Budget and Compliance Specialist will report directly to the ... and much more. Posted Job Title Clinical Trials , Billing, Budget and Compliance Specialist Job Profile Title Financial Analyst Job Description Summary Job… more
- University of Colorado (Aurora, CO)
- …Team (CReST) has an opening for a full-time Clinical Research Startup Specialist to provide regulatory and operationalization startup support for a variety ... communicates with these entities in order to operationalize complex clinical trials . + Develops standard operating procedures... Clinical Practice, applicable regulations, and of the clinical trial lifecycle is essential. We are… more
- Beth Israel Lahey Health (Boston, MA)
- …Type:** Regular **Scheduled Hours:** 40 **Work Shift:** Day (United States of America) The Clinical Trials Specialist II is responsible for fostering and ... to ensure disease groups have appropriate internal organization to effectively comply with regulatory requirements for clinical trials . Serves to provide… more
