Clinical Data Manager Jobs in Jersey City, New Jersey
65 Jersey City, NJ Clinical Data Manager jobs found on Monster.
The Manger, Risk Adjustment Data Validation supervises staff and processes associated with auditing clinical documentation that supports Healthfirst diagnoses submitted to CMS, New York State and other entities in support of appropriate risk scores of Healthfirst members. This position will oversee direct review of provider documentation and also completion of audits of vendors that Healthfirst co...
Great opportunity for an experienced Clinical Data Manager! Very stable and fast-growing pharmaceutical company! Long-term contract role! Excellent work environment! Candidate needs to have hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project. Experience in InForm, Oncology a plus. Indepen...
SAS/Statistician,Database Developer,Paralegal,Medical Writer,Data Manager,Clinical Manager,Outsource
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician (Some position can be telecommuting), Database Developer, Sr. Clinical Data Manager, Medical Writer, Clinical Manager, Paralegal, Outsourcing managers for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.c...
Statistician&SAS(remote),LSH–Oracle Clinical,Medical Writer,Clinical data manager,Biomarker Trial He
TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
Clinical Data Manager – Full Time Permanent position in Metuchen, NJ All work to be performed onsite. For additional details please email me your resume at – arati.kapileshwari@maxisit.com Must have Oncology experience and total of 5+ years of Data Management experience · Require MediData Rave or Inform experience. · e/CRF Design – Review and approve CRF design, data review ground rules and databa...
Nurse (LPN, RN, NP) Manager of Clinical Review Audits & RADV - Managed Care New York, NY (Manhattan) Job Summary: The Manager of Clinical Review Audits & Risk Adjustment Data Validation (RADV) supervises processes and staff associated with auditing clinical documentation that supports diagnoses submitted to federal, state, and other entities. This position will oversee the review of provider docum...
Global Pharmaceutical company is seeking a clinical project manager (PM) for a long term contract to provide Project Management and Continuous Improvement (CI) expertise (e.g. DFSS, Lean, Six Sigma) and aid in embedding a CI culture within Development Operations. The PM/CI Specialist leads the global development (and implementation as appropriate) of large-impact continuous improvement business pr...
A clinical research group at Columbia University Medical Center, Department of Medicine, Division of Endocrinology, is looking for a Clinical Research Manager to implement NIH and FDA sponsored clinical trials and manage a research coordinating staff. Looking for a resourceful and dynamic leader to join our group and lead our research staff. The Clinical Research Manager would be implementing prot...
Klein Management Systems
Florham Park, 07932
Expert Clinical Manager 6 month, renewable contract w2 candidates only Duties: Clinical trial management of studies under the management of the Clinical Trial Head (CTH)/Lead CTH including all study-related activities and CRO/ vendor management and oversight. Other duties include organizing/compiling/leading the preparation of various regulatory documents including CSR appendices, Investigator Bro...
LEO Pharma Inc. is a leading global pharmaceutical company specializing in dermatology and critical care. For 100+ years, our products have improved the quality of millions of people's lives around the world. Headquartered in Denmark, we have 4500 employees in 50+ countries and our products are sold in more than 100 countries. To realize our vision of becoming the world’s leading specialty pharmac...
Requisition ID 14487BR Title Regional Clinical Research Associate (CRA)- New York, NY Job Category Clinical Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaborat...
WE CURRENTLY HAVE SEVERAL CARE MANAGER POSITIONS AVAILABLE IN OUR MANHATTAN OFFICE. NEW HIRES EARN FOUR WEEKS VACATION WITHIN THEIR FIRST YEAR! VALUEOPTIONS OFFERS A GENEROUS COMPENSATION PACKAGE INCLUDING BENEFITS, TUITION REIMBURSEMENT, ETC. ABOUT OUR COMPANY ValueOptions® is a health improvement company that serves more than 32 million individuals. On behalf of employers, health plans and gover...
Clinical Research Nurse Duties: Responsible for working under the guidance of the CRC Medical Director; Principal Investigator and Sub-Investigators; Director, CRC Operations; Study Conduct Manager; and Clinical Research Coordinators to perform study procedures required in clinical research studies conducted on behalf of sponsors at the Frontage Clinical Research Center. Supervises: Laboratory Tec...
Comprehensive Clinical Development, Inc. (CCD) specializes in research, care management, and education related to central nervous system disorders. CCD actively invites collaboration and contact across multiple spheres, including academia, government agencies, and with members of the biopharmaceutical and commercial healthcare industries, as well as financial and investment communities. (Please vi...
Company Confidential
Berkeley Heights, NJ, 07922
We have several positions and are eagerly reviewing new candidates. Please submit your resume if you feel you meet the necessary requirements below: The Clinical Trials Associate (CTA) is involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Requirements: BA/BS in directly-relevant discipline or equivalent experience required At least 2 years experience as...
Requirements: Bachelor's degree 5-10 years of experience in clinical data management role Thorough knowledge of ALL of data management processes from study start up to study close out Previous experience in managing delivery of projects through full data management study life cycle (Phase I and II or Phase III) Experience working on both paper and electronic data management studies Direct experien...
Requirements: Bachelor’s degree 5 years experience as a data coordinator Strong documentation and project management skills Responsibilities: Act as point person for plan sponsor to provide responses to requests Evaluate and analyze data submitted by various parties to ensure it meets criteria set by the study protocol Monitor and update central database to ensure that all data is being process ti...
Responsible for Lead Data Management activities (study start up to database lock) for Phase 1 Oncology studies . Overseeing all CRO management including managing CRO deliverables and relationships at the study level . Overseeing development and review on all CDM study-related documents (i.e. CRFs, Data Management Plan, CRF completion guidelines, etc.). Performing in-house monitoring of data entry...
Clinilabs is a global, specialty CRO that provides services to companies involved in the clinical development of central nervous system (CNS), cardiovascular, and other therapeutics. The Company offers a full portfolio of contract research services, including project management, medical monitoring, study monitoring, data management, biostatistics, and electronic data capture. Clinilabs provides co...
Description Description: The incumbent is a field-based professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support for AstraZeneca's respiratory marketed products, new indications for current products, and compounds in development. The incumbent engages in scientific exchange with medical and scientific experts, including Healthca...
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Clinical Data Specialist
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Typical Salary for Clinical Data Specialist in Jersey City
(112 Respondents)
Source: Monster.com Careerbenchmarking Tool
Education / Training
Bachelor's
44.4%
Associates
16.7%
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Master's
11.1%
High School
5.6%
Certification
5.6%
Professional
2.8%
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Sample Resume for a Midlevel Clinical Data Specialist
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Sample Resume for an Entry-Level Clinical Data Specialist
Is your resume as optimized as the clinical data you code? This sample shows how you can organize your resume data to launch your career.
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.5.0.223-313