- Mount Sinai Health System (New York, NY)
- …Description** Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical ... in interpreting clinical research data. + Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the … more
- Mount Sinai Health System (New York, NY)
- …research studies , obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for eg, ... collection, specimen collection, obtaining informed consent, and maintaining and organizing study information. The Tisch Cancer Institute is a vital component of… more
- Mount Sinai Health System (New York, NY)
- …the medical order. Follows sleep center protocols related to the sleep study . 4. Upon patient arrival, verifies identification, collects documents and obtains ... consent for the study . 5. Explains the procedure and orients the patient...Latency Test (MSLT), Maintenance of Wakefulness Test (MWT), parasomnia studies , PAP and oxygen titration, etc.] to ensure collection… more
- Pfizer (Albany, NY)
- …beneficial customer-specific projects, collaborations, strategic medical partnerships, and non-interventional studies with the goal of advancing quality of care and ... as appropriate. The role may facilitate Pfizer sponsored research projects/ studies which could include collaborative projects, quality improvement research and… more
- IQVIA (New York, NY)
- …of ensuring high quality patient experience data (PED) are collected in clinical studies . Our PCS-I enhanced eCOA services include robust eCOA or digital design, ... analytical insights / monitoring of PED within a clinical study . Our approaches are rooted in behavioral science, clinical...and leading client projects to implement COAs in clinical studies . This role will manage project teams of scientific… more
- SUNY Upstate Medical University (Syracuse, NY)
- …through phase 3 trials. The role will be expected to manage 4 or more studies simultaneously. The CRA II will ensure compliance with FDA guidelines and follow GCP ... for all managed studies . The CRA II will interact daily with clinicians,...the candidate needs the ability to communicate directly with study volunteers, collecting detailed clinical information and communicating that… more
- Actalent (Bronx, NY)
- …compliance with institutional guidelines. Responsibilities + Coordinate the preparation of study tools, such as study binders, medication diaries, eligibility ... + Maintain comprehensive research records for all patients enrolled in studies , including patient consent, eligibility, Case Report Forms, and registration… more
- University of Rochester (Rochester, NY)
- …Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400274 CCRC Work Shift: UR - Day (United States of America) Range: UR URG 109 ... based on spending trends. + Manages subcontract process for large multicenter studies . + Gathers information, tracks the subcontract process with ORPA using IORA.… more
- SUNY Upstate Medical University (Syracuse, NY)
- …human through phase 3 trials. The role will be expected to manage 2-3 studies simultaneously. The will ensure compliance with FDA guidelines and follow GCP for all ... managed studies . The CRA I will interact daily with clinicians,...the candidate needs the ability to communicate directly with study volunteers, collecting detailed clinical information and communicating that… more
- Weill Cornell Medical College (New York, NY)
- Title: Research Nurse Practitioner Location: Upper East Side Org Unit: Nursing Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Exempt Salary Range: ... + Acts as a liaison between inpatient and outpatient units for study patients: works with referring physicians and their staff to ensure continuity… more