- Merck & Co. (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... internal policy, regulatory requirements, and health literacy principles.With minimal oversight, the Senior Informed Consent Medical Writer:Demonstrates… more
- Merck & Co. (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... policy, regulatory requirements, and health literacy principles.With oversight, the Informed Consent Medical Writer:Demonstrates growing independence… more
- Merck (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
- Merck (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
- Citigroup (New York, NY)
- …data flows to support our Enterprise risk functions including board and senior management reporting. This will include understanding the current and developing ... policies, guidelines and procedures. **About the role:** The Business Senior Lead Analyst role is responsible for ensuring timely...scope and commitments of each phase of the Risk Consent Order Data Quality Plans to ensure proof of… more
- Vitalief (New Brunswick, NJ)
- …CRC will perform protocol-specific tasks including: Surgical patient screening, obtaining informed consent , collection of protocol required imaging, IRB ... Operating Procedures (SOPs), and create SOPs as needed (ie, process for obtaining informed consent ; study subject data collection process, etc.). + Follow and… more
- Mount Sinai Health System (New York, NY)
- …protocol amendments, and renewals of ongoing clinical trials. + May obtain informed consent under general supervision of the Investigator(s) and educate ... of leaders in the field. Under general supervision, The Sr . Clinical Research Coordinator analyzes and interprets highly complex...Sinai Health System is one of the largest academic medical systems in the New York metro area, with… more
- Mount Sinai Health System (New York, NY)
- …Investigator or senior clinical research staff. This individual obtains informed consent , collects, maintains and organizes study information. Assists in ... related to clinical research including, but not limited to: obtaining informed consent , screening participants for eligibility, registering patients with… more
- Mount Sinai Health System (New York, NY)
- …eligibility, registering subjects with sponsoring agency, administering questionnaires. Obtaining informed consent under minimal supervision and educating ... related to clinical research including, but not limited to: obtaining informed consent , screening participants for eligibility, registering patients with… more
- Mount Sinai Health System (New York, NY)
- …submissions, protocol amendments, and renewals of ongoing clinical trials. 6. Obtains informed consent under supervision of the Principal Investigator, Clinical ... Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects,...and for studies involving genetic tests. 7. Independently obtains informed consent for other clinical studies. 8.… more
