- Merck & Co. (Rahway, NJ)
- Job DescriptionWith support of Sr CRA ( Clinical Research Associate) and/or CRA Manager, acts as primary site contact and site manager-throughout all phases of a ... clinical research study, taking responsibility of allocated...on-site monitoring & oversight activities using various tools to ensure: Data generated at site are complete, accurate and unbiasedSubjects'… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- … methods, techniques and procedures in performing research .Ensures proper compliance with Institutional Review Board ( IRB ) and other regulatory ... confidentiality, and privacy protections.Coordinates with PI to help ensure that clinical research and related activities are performed consistently with… more
- Cedars-Sinai (Los Angeles, CA)
- …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical ... known nationally for excellence in research !** The Clinical Research Data Specialist III...including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties… more
- Cedars-Sinai (Los Angeles, CA)
- …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . - Maintains research practices using Good Clinical ... bioinformaticians focused on high impact cardiovascular clinical research . As a Clinical Research Data Specialist I, you will manage the data for… more
- Cedars-Sinai (Santa Monica, CA)
- …Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties and Responsibilities** *Supervise clinical research data ... team and contribute to groundbreaking research !** The Clinical Research Data Associate III...and education programs. *Works closely with study monitors to review study data and respond to inquiries.… more
- Cedars-Sinai (Los Angeles, CA)
- …with an organization known nationally for excellence in research !** **JOB SUMMARY:** The Clinical Research Data Specialist III manages the data for ... Ensures compliance with all federal and local agencies including Institutional Review Board . **ESSENTIAL JOB...the most. **Req ID** : HRC1338274A **Working Title** : Clinical Research Data Spec III… more
- Cedars-Sinai (Los Angeles, CA)
- …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical ... known nationally for excellence in research !** The Clinical Research Data Specialist II...including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties… more
- Cedars-Sinai (Los Angeles, CA)
- …of the top hospitals in California and in the nation by US News & World Report. The Clinical Research Data Specialist II manages the data for assigned ... including the Food and Drug Administration (FDA) and local Institutional Review Board . \#Jobs-Indeed **_*This...the most. **Req ID** : 1915 **Working Title** : Clinical Research Data Specialist II… more
- Cedars-Sinai (Los Angeles, CA)
- …use your skills with an organization known nationally for excellence in research !** The Clinical Research Data Specialist I manages the data for ... Ensures compliance with all federal and local agencies including Institutional Review Board . Our team...cardiovascular clinical research . As a Clinical Research Data Specialist I,… more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient ... invention and teamwork. Research | Cedars-Sinai The Clinical Research Data Specialist I...(FDA) and local Institutional Review Board . **ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:** Manages data… more
- Cedars-Sinai (Los Angeles, CA)
- … clinical research data , and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I may have limited contact ... follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB...Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP)… more
- Cedars-Sinai (Los Angeles, CA)
- …Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... data , and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP)… more
- Cedars-Sinai (Los Angeles, CA)
- …*Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising research staff or directly with the ... data , and assist with regulatory submissions to the IRB . Provides limited patient contact with research ...Institutional Review Board . Maintains research practices using Good Clinical Practice (GCP)… more
- Cedars-Sinai (Los Angeles, CA)
- … clinical research data , and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I may have limited contact ... Responsibilities:** + Completes Case Report Forms (CRFs). + Enters clinical research data into Electronic...patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... objectives. Responsible for completing case report forms, entering clinical research data , and assist...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP) guidelines. *Maintains strict patient ... objectives. Responsible for completing case report forms, entering clinical research data , and assist...follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP) guidelines. *Maintains strict patient ... objectives. Responsible for completing case report forms, entering clinical research data , and assist...follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... objectives. Responsible for completing case report forms, entering clinical research data , and assisting...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- Cedars-Sinai (Beverly Hills, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... responsible for completing case report forms (CRFs) and entering clinical research data , as well...and Drug Administration (FDA) and local Institutional Review Board . + Maintains research … more
- Cedars-Sinai (Los Angeles, CA)
- …(FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical Practice (GCP) guidelines. *Maintains strict patient ... responsible for completing case report forms (CRFs) and entering clinical research data , as well...follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board ( IRB… more
