Clinical Research Jobs in Newark

Job Description Clinical Research Coordinator Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study. Responsible for all..

Job Description Job Responsibilities: Updating the Clinical Trials Management System (CTMS) as needed with location profile information (CVs, medical licensures, laboratory accreditations), IRB status, consent form versions (protocol/consent form evolution),..

OverviewnAtlantic Health System is currently seeking a full-time Clinical Nursing Coordinator in the Neuroscience Research Department at Overlook Medical Center working from 8 AM to 4PM, weekends not required.nResponsibilitiesnEssential Functions:n..

Job Location: East Hanover, NJ Well know manufacturer of medical lab analyzers is in need of a Hotline Support Manager at their Northern New Jersey location. Will be responsible for..

You may be eligible to apply for the Education Debt Reduction Program if funds are available.nnThis is considered the full performance level for nonsupervisory positions. A MT at this level..

Company OverviewnAt Memorial Sloan Kettering (MSK), weu2019re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward..

Job DescriptionnnOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our..

Job Description Clinical Research Coordinator Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study. Responsible for all..

Save Skills Excel Microsoft Word Clinical Trials Microsoft Powerpoint Clinical Research Req #: 1902956 Location: Summit, New Jersey, United States Job Category: Medical Work Location: 86 Morris Avenue 07901 Organization:..

Job DescriptionnnOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products...

Company OverviewnAt Memorial Sloan Kettering (MSK), weu2019re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward..

Job DescriptionnnOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products...

Save Education Bachelor's Degree Skills Clinical Laboratory Experience Laboratory Experience PRIMARY PURPOSE: Under the general direction of the Laboratory Supervisor of the Cord Blood Department, the Laboratory Technologist/Technician will be..

Company OverviewnAt Memorial Sloan Kettering (MSK), weu2019re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward..

Job DescriptionnnOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products...

OverviewnAt New York Blood Center, one of the most comprehensive blood centers in the world, our focus is on cultivating excellence by merging cutting-edge innovation with diligent customer service, groundbreaking..

Save Education Bachelor's Degree Master's Degree Skills Microbiology Clinical Research New York University: NYU - Domestic: College of Dentistry: Basic Science and Craniofacial Biology Location New York Open Date Aug..

Job Description We are looking for a Clinical Research Regulatory Affairs coordinator to join our team. Job Responsibilities: Updating the Clinical Trials Management System (CTMS) as needed with location profile..

Medical Data Scientist The incumbent must have at least 2 years of clinical data review experience in Clinical Research, review protocol and CRF designs.Adequate knowledge of ICH guidelines.Abstracts all necessary..

The Core Lab Supervisor is responsible for the following laboratory sections: Hematology, Chemistry, Diagnostic Immunology, Endocrinology, Oncology, Clinical Toxicology, and Urinalysis. The supervisor will perform the expected responsibilities of the..

Title: Clinical Trial Associate nLocation: Leesburg, VA nSchedule: 8am to 5pm Mon – Fri. nStart date: ASAP nResponsibilities: n n Coordinates with Clinical Affairs department and cross-functional departments to ensure..

This position is responsible for performing and interpreting automated and manual testing procedures on blood, urine, and other body specimens. This position does not involve direct patient care for a..

Save Education Bachelor's Degree Skills IIS Clinical Trials Clinical Research Title: Clinical Trial Associate Location: Leesburg, VA Schedule: 8am to 5pm Mon – Fri. Start date: ASAP Responsibilities: Coordinates with..