Full-Time Senior Clinical Research Associate jobs in New Jersey

Now available 5 results are consistent

Sort by:relevance - date

SENIOR CLINICAL RESEARCH ASSOCIATE- KANSAS (REMOTE)

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &...

CompanyMerck Sharp Dohme
AddressRahway, NJ
CategoryEducation/Training
Date Posted 2 weeks ago See detail

Senior Clinical Research Associate- Kansas (REMOTE)

Merck Sharp Dohme

Rahway, NJ

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &...

Senior Clinical Research Associate

Everest Clinical Research Usa

Bridgewater, NJ

$97.5K - $123K a year

Interact with personnel from study sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high quality initiations and completions of clinical trials. Identify, evaluate and qualify investigat...

Senior Clinical Research Associate- Florida (REMOTE)

Merck Sharp & Dohme

Rahway, NJ

$122,800 - $193,300 a year

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &...

Associate Clinical Scientist, Oncology (Senior Manager)

Biospace

Princeton, NJ

Supports execution of assigned clinical trial activities and works closely with Clinical Scientist to execute activities associated with trial conduct. Supports trial level activities for one or more trials with the necessary supe...

Clinical Research Associate- Minnesota (Remote)

Merck Sharp & Dohme

Rahway, NJ

$91,600 - $144,100 a year

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &...