- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist II /III as part of the Quality Operations team based in Raritan, ... New Jersey. Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a… more
- Cedars-Sinai (Los Angeles, CA)
- …patient outcomes. **Are you ready to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned ... Collaborates with bioinformatics in the development and maintenance of clinical trials management systems including validation of...and experience. **Req ID** : 10946 **Working Title** : Clinical Research Data Specialist II … more
- Cedars-Sinai (Los Angeles, CA)
- …more about the Butte Lab, please visit this website . **About the Role** The Clinical Research Data Specialist II manages the data for assigned research ... work with bioinformatics in the development and maintenance of clinical trials management systems including validation of...the most. **Req ID** : 11995 **Working Title** : Clinical Research Data Specialist II … more
- Cedars-Sinai (Los Angeles, CA)
- …and use your skill with an organization known nationally for excellence in research!** The Clinical Research Data Specialist II manages the data for assigned ... work with bioinformatics in the development and maintenance of clinical trials management systems including validation of...and experience. **Req ID** : 12237 **Working Title** : Clinical Research Data Specialist II … more
- Huron Consulting Group (Van Buren, AR)
- …will make you a key member of Huron's Research Office Team. As a Clinical Research Administrative Specialist II , you'll assist Huron's Research Office ... to expand upon your working knowledge and experience with clinical trial regulation, and to develop strong...budget development & negotiation experience is highly desired + Clinical Trials Policy and Research Billing Rules… more
- Huron Consulting Group (Van Buren, AR)
- …will make you a key member of Huron's Research Office Team. As a Clinical Research Administrative Specialist II , you'll assist Huron's Research Office ... to expand upon your working knowledge and experience with clinical trial regulation, and to develop strong...related items, and milestones for both new and legacy clinical trials in CTMS. + Coverage Analysis… more
- Dana-Farber Cancer Institute (Brookline, MA)
- … clinical trial data, national protocol and investigator registrations, clinical trials education, and committee management. The Associate Director of ... Specialists and reports to the Director of ODQ. The Clinical Research Systems Specialist II ...+ Perform randomization and registration of clinical trial subjects for DF/HCC investigator-sponsored, randomized trials .… more
- Cleveland Clinic (Cleveland, OH)
- …care, our providers are national or global leaders in cancer research, which include clinical trials and laboratory based research. We believe clinical ... Governing Body of the applicable hospitals. **CNS** + Currently licensed as a Clinical Nurse Specialist in applicable state(s). + Must be licensed as an RN in… more
- Stony Brook University (Stony Brook, NY)
- Research Nurse - Cancer Clinical Trials **Position Summary** The **Research Nurse** for the Cancer Center Clinical Trials Department is responsible for ... AE logs, con meds, etc.) in source material, and enter necessary information into Clinical Trial Management System (CTMS). + Assist with organizing, and attend… more
- AdventHealth (Orlando, FL)
- …in support of research under the auspices of AdventHealth. The Contract Specialist II is knowledgeable in the area of clinical trial agreement contract ... Time **Shift** : Days **Location:** 601 EAST ROLLINS STREET, Orlando, 32803 **The role you'll contribute:** The Contract Specialist II will play a vital role… more
- Hartford HealthCare (Hartford, CT)
- …policies for protocol deviations, safety reporting and continuing reviews. * Assist research account specialist of CCRO with clinical trial billing in the ... and ensures the data quality and integrity for each clinical trial . Responsibilities: * Coordinate and facilitate...system alliances. * Coordinate and conduct the operation of clinical trials as per GCP and ICH… more
- Deschutes County (Bend, OR)
- Behavioral Health Specialist II , Civil Commitment Investigator/Monitor Print (https://www.governmentjobs.com/careers/deschutes/jobs/newprint/5095838) Apply ... Behavioral Health Specialist II , Civil Commitment Investigator/Monitor Salary $6,004.15...Community Mental Health Program providing safety net and core clinical services for community members in Deschutes County dealing… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Controlled Substance Specialist II ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... Solutions in Kansas City, MO is hiring Controlled Substance Specialist II .** The **Controlled Substance Specialist...sizes to advance new medicines from early development to clinical trials and to the market. Catalent… more
- Catalent Pharma Solutions (Chelsea, MA)
- **Quality Assurance Specialist II , Operations** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization ... Catalent Pharma Solutions is hiring a Quality Assurance (QA) Specialist II . The Quality Assurance Specialist...sizes to advance new medicines from early development to clinical trials and to the market. Catalent… more
- Cedars-Sinai (Los Angeles, CA)
- …or Contract Research Organization (CRO). + 5 years of experience in Phase I, II , III, IV clinical trials and investigator-initiated trials ... and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal… more
- University of Rochester (Rochester, NY)
- …and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The CHeT Communication Specialist II is responsible for the creation, development, and ... English grammar and scientific terminology Required + Proficiency in interpreting clinical trial data and writing in compliance with regulatory and scientific… more
- Cedars-Sinai (Los Angeles, CA)
- …+ Finds opportunities for research funding opportunities. + May negotiate budgets for clinical trials . + May assist with research participant billing. + ... Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality...**Req ID** : 11255 **Working Title** : Research Grant Specialist II - Department of Medicine -… more
- Bristol Myers Squibb (Summit, NJ)
- …used in the production of personalized cell therapy products for both global clinical trials and commercial supply. The incumbent must be self-directed, ... and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
- PACIV (Indianapolis, IN)
- …tailored to regulated environments. We are seeking a detail-oriented and proactive Validation Specialist II for our Indianapolis, IN office to support compliance ... + Execute Periodic Reviews of all departmental computerized systems supporting Clinical Trials (ie Parts Washers, Autoclaves, Filtration Systems, etc.)… more
- Methodist Health System (Dallas, TX)
- …for clinical trials assigned. * Assist in the development of clinical trial documents for signature of principal investigator and approval by the IRB. ... trials to include, but not limited to; Phase II and IV clinical , investigator initiated ...initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support… more
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