Clinical Data Coordinator Jobs in New Jersey

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796 New Jersey Clinical Data Coordinator jobs found on Monster.

Jobs 1 to 20 of 796
TechData is looking for Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting),Health Economics & Outcomes Research(HEOR Biostatistician), Manager of Sales Analytics Positions, Clinical Research Scientist/Development Specialist, Drug Safety Specialist/Trial Safety Manager,Sr. Clinical Data Manager for our pharmaceutical clients inNorthern NJ.Please see below requirements...
TechData is looking for Biostatistician (Contract/permanent, or remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Programmer, Pharmacovigilance, Outsourcing Manager, Medical Doctor, Clinical Data Manager, Informed Consent Form Specialist, Clinical Research Scientist, Safety Scientistfor our pharmaceutical clients in Northern and Central NJ. Please see below requi...
Covance Newark, NJ
Imagine working in one of the most exciting and professionally satisfying industries anywhere. Imagine being involved in cutting-edge projects on a daily basis. At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world’s largest and most respected contract research organizations. Our clients ...
Job Summary and Responsibilities: The Clinical Data Coordinator maintains essential study documents for clinical research studies and enters data onto Case Report Forms and ensures study compliance. 1. Prepares reports and assists with statistical analysis. 2. Maintains regulatory binders in accordance with FDA guidelines. Assists research nurse in the preparation of all audits performed by var...
Clinical Data Associateneeded for acontractopportunity with Yoh's client located inBridgewater, NJ. What You'll Be Doing: - Interact both verbally and through written communication with inter-organizational and outside customer contacts as well as with Central and External laboratories, CROs, etc. - Contribute to the design of protocols - Develop eCRF specifications according to protocol and a...
Description: Position Description: Energize your career with one of Healthcare's fastest growing companies. You dream of a great career with a great company where you can make an impact and help people. We dream of giving you the opportunity to do just this. And with the incredible growth of our business, it's a dream that definitely can come true. Already one of the world's leading Healthcare ...
Description: Position Description: Energize your career with one of Healthcare's fastest growing companies. You dream of a great career with a great company where you can make an impact and help people. We dream of giving you the opportunity to do just this. And with the incredible growth of our business, it's a dream that definitely can come true. Already one of the world's leading Healthcare ...
Description: Position Description: Energize your career with one of Healthcare's fastest growing companies. You dream of a great career with a great company where you can make an impact and help people. We dream of giving you the opportunity to do just this. And with the incredible growth of our business, it's a dream that definitely can come true. Already one of the world's leading Healthcare ...
Assist in resolving coding and billing edits that are holding patient claims from final billing. Maintain the integrity of Charge Description Masters (CDM) and Revenue Integrity Systems Programs. Maintain the integrity of all Ancillary Department systems related to billing and revenue. Position will serve as liaison between Administration, and Ancillary Department Directors regarding revenue and c...
Assist in resolving coding and billing edits that are holding patient claims from final billing. Maintain the integrity of Charge Description Masters (CDM) and Revenue Integrity Systems Programs. Maintain the integrity of all Ancillary Department systems related to billing and revenue. Position will serve as liaison between Administration, and Ancillary Department Directors regarding revenue and c...
Artech Information Systems East Hanover, NJ
Job Summary Company: Artech Information Systems LLC Position: Clinical Data Support Associate Location: East Hanover ,NJ Job Reference Code: 15-02761 JOb Description: Set up and maintain clinical activities using project tracking tools by coordinating with and supporting clinical teams. Obtain and track trial specific information according to clinical development plans. Accurate and timely...
Covance is seeking a Clinical Data Manager to work from our Princeton, NJ office. The Clinical Data Manager will serve as the technical leader on all data management aspects for project(s) including start-up, maintenance, and completion activities. Essential Job Duties Include: • Develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consiste...
Review study protocols and provide input from a data management perspective Work in conjunction with Project Manager or Manager on CRF/EDC design process utilizing data form standards. In collaboration with Project Manager or Manager, create CRF completion guidelines to be utilized by sites and Clinical Research Associates. Work with team and /or vendor to set up, validate and maintain clinical...
Stryker Communictions Mahwah, NJ
Review study protocols and provide input from a data management perspective Work in conjunction with Project Manager or Manager on CRF/EDC design process utilizing data form standards. In collaboration with Project Manager or Manager, create CRF completion guidelines to be utilized by sites and Clinical Research Associates. Work with team and /or vendor to set up, validate and maintain clinical...
Marten Transport Princeton, NJ
Senior Clinical Data Manager Established CRO in greater Princeton area has an immediate need for a perm Clinical Data Manager. Onsite role. CORE RESPONSIBILITIES: Act as lead data manager on multiple studies of moderate complexity with minimal supervision Main point of client contact for all DM related matters Execute all DM start-up activities, including the development and maintenance of C...
Marten Transport Princeton, NJ
Established CRO in greater Princeton area has an immediate need for a perm Clinical Data Manager. Onsite role. CORE RESPONSIBILITIES: Act as lead data manager on multiple studies of moderate complexity with minimal supervision Main point of client contact for all DM related matters Execute all DM start-up activities, including the development and maintenance of Conduct user acceptance testing...
Job Juncture, Inc. Princeton, NJ
Our client, a well established international contract research organization serving both commercial as well as government markets, is conducting a search for a full time Direct Hire Clinical Data Manager to be based at the company's headquarters in Princeton NJ. The successful candidate will possess a forward-thinking approach and be able to anticipate challenges and proactively implement solutio...
Clinical Data Manager Bridgewater, NJ
Apply Now ? Apply to this Job Attach your resume By providing us with your information, you agree to become a Bullhorn Reach User, and to our use and disclosure of your information as described by our Privacy Policy. Job Description Clinical Data Manager-Bridgewater,NJ Contract position-5 months Send resumes to: ***** Duties Interact both verbally and through written comm...
Net-Temps Bridgewater, NJ
Job Title: Clinical Data Manager Duties: Interact both verbally and through written communication with inter-organizational and outside customer contacts as well as with Central and External laboratories, CROs, etc. -Contribute to the design of protocols -Develop eCRF specifications according to protocol and approved standards (based on industry standards), participate in user acceptance testing...
Artech Information Systems Bridgewater, NJ
Company: Artech Information Systems LLC, Industry: Pharmaceutical Position Title: Clinical Data Manager Location: Bridgewater, NJ Job Reference Code: 14-47715 Duties: Interact both verbally and through written communication with inter-organizational and outside customer contacts as well as with Central and External laboratories, CROs, etc. -Contribute to the design of protocols -Develop eCRF...

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