- Merck & Co. (Rahway, NJ)
- …/ portfolio management. - Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (Rahway, NJ)
- …/ portfolio management.-Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable.-Preferred Experience and Skills: ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Catalent, Inc. (Kansas City, MO)
- …Quality Assurance Senior Specialist . The Supplier Quality Assurance Senior Specialist will assure compliance to national and international standards by ... Supplier Quality Assurance Senior Specialist Position Summary Catalent, Inc. is a leading...Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range… more
- The University of Pennsylvania (Philadelphia, PA)
- …Department of Operations, Compliance and Monitoring (DOCM) is seeking a The Clinical Research Quality Specialist , Sr. to support our clinical research ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Monitoring and Auditing Specialist (Abramson Cancer Center) Job… more
- Abbott (Alameda, CA)
- …meeting project commitments and in compliance with applicable regulations, good clinical practice ( GCP ) and standards. **_What you will do:_** + Assist ... Research team in Alameda, CA is adding a Clinical Operations Data Specialist to our Team....clinical operations activities in accordance with applicable regulations; GCP , policies and procedures. May include the following activities:… more
- Caris Life Sciences (Phoenix, AZ)
- …bigger than yourself, Caris is where your impact begins.** **Position Summary** The Clinical Study Documentation Specialist provides clinical study support ... sponsor touchpoints, to provide updates on study status and clinical study documentation timelines. + Support compliance ...30 lbs as needed. **Training** + Completion of Good Clinical Practices ( GCP ), Human Subject Protection, and… more
- Terumo Neuro (Aliso Viejo, CA)
- **12870BR** **Title:** Sr Specialist , Clinical Trial Quality Assurance **Job Description:** Provide support to all aspects of the Clinical Quality Assurance ... reporting, root cause analysis investigation, and closure. Provide comprehensive compliance direction to clinical study teams and...2. Minimum of four (4) years of experience in clinical research and/or GCP related QA environment… more
- University of Southern California (Los Angeles, CA)
- …and with agencies including the IRB and Federal Drug Administration (FDA). Maintains compliance with Good Clinical Practice ( GCP ) guidelines, patient ... Clinical Research Regulatory SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research-Regulatory- Specialist \_REQ20164101-1/apply) Keck School of Medicine Los… more
- Stony Brook University (Stony Brook, NY)
- Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer Clinical Trials Office **Investigator Initiated Trial Specialist ... Research Team meetings. + Maintaining research practices in accordance with Good Clinical Practice ( GCP ) guidelines, ensuring strict patient confidentiality as… more
- University of Pennsylvania (Philadelphia, PA)
- …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 Abramson Cancer Center...study team meetings, research team meetings, and ongoing protocol training/ compliance meetings. The Regulatory Affairs Specialist -CC is… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Clinical Research Data Specialist to work at the UHealth Medical Campus in ... Miami, Fl CORE JOB SUMMARYThe Clinical Research Data Specialist assists in creating,...compliance with CRS and UM policies, the protocol, ICH- GCP , and federal regulations. + Provides support with study… more
- Cedars-Sinai (Los Angeles, CA)
- …outcomes. **Are you ready to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research ... data, maintaining record systems, and producing project reports for studies. The Specialist also trains clinical research staff, perform basic statistical… more
- Cedars-Sinai (Los Angeles, CA)
- …trials (IITs) and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role ... to coordinate all aspects of assigned investigator-initiated and multi-site projects. The Clinical Research Specialist II provides clinical research… more
- SUNY Upstate Medical University (Syracuse, NY)
- …This role will also provide ongoing education and mentorship to CRAs to ensure compliance with Good Clinical Practice ( GCP ), FDA regulations, and sponsor ... Job Summary: The Clinical Trails Specialist (Cancer Center Focus)...of education and experiance. Strong knowledge of FDA regulations, ICH- GCP guidelines, and clinical trial budgeting. Excellent… more
- J&J Family of Companies (Atlanta, GA)
- …preferred but not required. + Working knowledge of clinical research, Good Clinical Practice ( GCP ) and regulatory compliance guidelines for clinical ... States **Job Description:** Johnson & Johnson is hiring for a **Field Clinical Specialist ** for Shockwave Medical Inc. located in **Atlanta, GA** . At Johnson… more
- Cedars-Sinai (Los Angeles, CA)
- …as well as their variation in health and disease. **About the Role** The Clinical Research Data Specialist II independently manages data for assigned research ... data, maintaining record systems, and producing project reports for studies. The Specialist also trains clinical research staff, perform basic statistical… more
- Cedars-Sinai (Los Angeles, CA)
- …an unparalleled environment for fostering invention and teamwork. Research | Cedars-Sinai The Clinical Research Data Specialist I manages the data for assigned ... local Institutional Review Board. Maintains research practices using Good Clinical Practice ( GCP ) guidelines. Maintains strict patient...job functions. **Req ID** : 4169 **Working Title** : Clinical Research Data Specialist I - PER_DIEM… more
- Caris Life Sciences (Phoenix, AZ)
- …to the appropriate group. + Responsible for ensuring sample integrity and maintaining Good Clinical Practice ( GCP ) compliance for samples through chain of ... Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist provides operational and regulatory...and IATA training. + All job specific, safety, and compliance training are assigned based on the job functions… more
- University of Miami (Miami, FL)
- …. The Department of Surgery has an exciting opportunity for a (Temp/Part-Time) Clinical Research Data Specialist position. The incumbent assists in enrolling ... supervision of the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist is responsible for...Human Subject Research, Group 1: Biomedical Researchers (HSR), good Clinical Practice ( GCP ) and Conflict of Interest… more
- Houston Methodist (Houston, TX)
- …and study specific protocols/plans and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case ... At Houston Methodist, the Regulatory Compliance Specialist position is responsible for...specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices ( GCP… more
