- 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
- Citigroup (New York, NY)
- …focus remains on the scope and commitments of each phase of the Risk Consent Order Data Quality Plans to ensure proof of Risk Reduction. Requires thorough ... skills in order to negotiate internally, often at a senior levels. Diplomacy skills are required in order to...initiatives and data capabilities. + Be a trusted and informed advisor/partner to regional teams and lines of business… 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
- Weill Cornell Medical College (New York, NY)
- …and guidelines and internal SOPs. + Assists with eligibility assessment and informed consent process, as appropriate. Performs central subject registration for ... with exposure to a team research environment at all levels ( senior investigators, nurses, research coordinators, lab technicians). **Knowledge, Skills and… more
- Pfizer (New York, NY)
- …other clinical and medical colleagues, with authoring protocols, study level informed consent documents, site training materials, and other clinical and ... disease area(s) of assignment. + Support other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
- Pfizer (New York, NY)
- …integrity and quality of the clinical trial(s). + Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site training ... area(s) of assignment. + Partners with other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
- Mount Sinai Health System (New York, NY)
- …related to clinical research including, but not limited to: obtaining informed consent , screening participants for eligibility, registering patients with ... wanting research experience before applying for graduate school or medical school. Our team has a strong track record...project, under direct supervision of the Principal Investigator or senior clinical research staff. + Assists in the activities… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …accurately and in understandable terms, complex medical information from medical providers to patients, including interpretation of consent forms, diagnoses, ... teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across… more