Clinical Research Associate — Translational Trials
Hackensack Meridian Health Inc.
Hackensack Meridian Health Inc. is seeking a Clinical Research Associate in Nutley, New Jersey. This position involves facilitating direct patient care, supporting the research team with patient recruitment and retention, and performing clerical duties. The ideal candidate will possess a Bachelor's degree in a related field or equivalent experience. Preferred qualifications include a Master's degree and relevant certifications. Strong personal management and communication skills are essential for success in this dynamic environment. #J-18808-Ljbffr Hackensack Meridian Health Inc.
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...implementation, on-site monitoring of clinical research studies as well as on-going... ...maintains study specific trial management tools/systems,... ..., as appropriate, translation of study related documentation... .... Verifies issues or risks associated with blinded or randomized...Contract workLocal areaRemote workNight shift- ...opportunities for growth and professional excellence. Job Description Associate degree or higher preferred Experience: 1-2 year relevant... ...in pharmaceutical industry or CRO Experience supporting clinical trials preferred Qualifications Knowledge, Skills, and Abilities Basic...Permanent employment
$75k - $85k
...patients, with the wrong assumptions, in trials that couldn't answer the real question:... ...ships. Every function at Pathos — from clinical execution to asset selection to the... ...contact between Pathos and CRO Clinical Research Associates for day-to-day trial communications Coordinate...Work at officeLocal area3 days per week- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...
$50 - $60 per hour
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- Overview Clinical Research Associate (II - Sr) - Sponsor Dedicated - Home-Based & Regionally Aligned Across... ...to accelerate customer success. We translate unique clinical, medical affairs and... ...functional teams to support clinical trial operations, including working with...Work at officeRemote workWork from homeFlexible hours
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$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote... ...the month and be responsible for monitoring and clinical trials across the region for a leading Clinical Research Organization...Permanent employmentWork at officeRemote work- ...Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic... ...level Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations...Work visa
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated Location: Gloucester, United States of America | Full time | Field-based | R1541733 To be eligible... ...as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File...Full timePart timeLocal areaImmediate start- ...Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate... ...based on findings. Responsibilities Develop and write trial protocols (outlining purpose and methodology) Present trial...RelocationVisa sponsorship
- ...an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health. Aligned... ...Responsibilities The primary purpose of the Clinical Research Associate position is to serve as a member of a multidisciplinary...Seasonal workWork at office
$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry... ...partnering closely with investigative sites to ensure high-quality trial execution. Responsibilities Perform routine and close-out...Permanent employmentRemote work
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