Clinical Data Coordinator Jobs in Bridgewater, New Jersey
14 Bridgewater, NJ Clinical Data Coordinator jobs found on Monster.Jobs 1 to 14 of 14
SOCIAL SERVICE – NEW PROFESSIONAL POSITION AVAILABLE!! – NEW BRUNSWICK, NJ Prevent Child Abuse - NJ We are the statewide leader in the prevention of child abuse and neglect for all of New Jersey’s children with over 30 years of prevention programming experience. We are proud to have been selected for a special 2 year grant to prevent human trafficking in NJ minors by providing training and prevent...
ExamWorks is a dynamic, fast growing global industry pioneer in the health care services sector. Our size, scale and service capabilities, combined with management's vision are transforming the IME industry. We are convinced that the high growth environment, the largest global geographic footprint and most advanced IT platform available differentiates ExamWorks from other IME companies. The compan...
Coordinator, Pharmacovigilance Operations - Princeton, NJ Experience in case processing preferred Experience in narrative writing preferred Educational Requirements: " Associate degree in a health related field is preferred, but not required. Experience: " 1-2 years of experience in the entry and coordination of adverse event data in a pharmaceutical company. Primary Skills and Abilities: " Attent...
BioClinica, Inc. is looking for intelligent, creative and dedicated professionals to join our growing team. We are company that values technical excellence, teamwork and commitment to success. We employ cutting edge technology to provide our customers with industry leading solutions and currently seeking to fill the position of Project Coordinator to work out of our Princeton, NJ office. Primary r...
Job Summary: The Clinical and Exploratory Pharmacology (CEP) Clinical Trial Manager (CTM) is responsible for the overall operational planning and activities for the implementation and conduct of clinical exploratory pharmacology clinical trials in compliance with ICH, GCP’s, SOPs, local requirements, internal/departmental guidelines, and established timelines. The CTM is involved in the operationa...
The Medical Operations Group 2 team is responsible for phase 2/3/4 clinical research studies conducted in Immuno-inflammation and Infectious Diseases. The proposed position will be focused on key phase 2B/3 clinical studies in autoimmune and/or respiratory conditions. Key accountabilities of the Clinical Study Director: • The CSD is the study leader/study champion. The main responsibility of the C...
Position in the organization: Clinical Study Director (CSD), reporting to Associate VP, Group Leader of Medical Operations Group 2 in the Medical Operations Department within the Clinical Sciences & Operations platform/ CSO. The Medical Operations Group 2 team is responsible for phase 2/3/4 clinical research studies conducted in Immuno-inflammation and Infectious Diseases. The proposed position wi...
JOB DESCRIPTION : FOUNDATION CLINICAL TRIAL MANAGER/COORDINATOR General Responsibilities: The Foundation conducts clinical trials and participates in governmental and nongovernmental clinical trials. Under the general direction of Medical Director, this individual is responsible for the development, execution and data management of clinical trials/studies. The research studies are in the field of...
Job Summary Manage multi-center clinical trials from start up to close out, in the U.S. or O.U.S. as applicable. For IDE/PMA studies, contribute to FDA approval process. Participate in the development/implementation/management of registries or other post approval/marketing activities as needed. Desired Skills & Experience • Write Investigational Plan (including CRFs, labeling, etc.), with support...
Green Key Resources is seeking Drug Safety/PV professionals in the Princeton, NJ area for the below opportunity. Position Summary: This position has coordination and administration responsibilities for a wide variety of Pharmacovigilance activities for all drug development programs at Client. Responsibilities include the adverse event data entry, tracking, report generation and submission, records...
A highly reputable and distinguished pharmaceutical corporation is looking for experienced professionals to work as Medical Records Extraction Coordinators in Whippany, NJ. Medical Records Extraction Coordinators in Whippany, NJ. Major Tasks and Responsibilities: Case prioritization based on seriousness of adverse events in accordance with SOPs (Standard Operating Procedures) and regulatory guidel...
The Director of Nursing is responsible for the day to day coordination and oversight of all aspects of the Nursing Department in accordance with current Federal, State and local regulations. Reporting to: The Director of Nursing directly reports to the Administrator of the facility, providing Nursing Services to coordinate nursing specific and clinical programs. The Director of Nurses has a dotted...
Experience: Must have Oncology and/or Hematology experience. It is preferred to have protocol and CSR writing experience. 5+ years of pharmaceutical experience in clinical trials. Must have an understanding of CRO/vendor management, clinical study design, CRF design, project management and familiarity with data handling. Serves as the coordinator for implementation of all clinical trial activities...
Position Responsibilities: The incumbent will execute end-to-end process activities including daily interactions with healthcare providers, medical record review, document processing, and data verifications. Responds to healthcare providers and internal/external customer's calls and requests within team-defined parameters. The DRG Validator reports to the Health Information Management Director and...
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Summary of Qualifications: Delivery of superior customer service and support. Provided optimal assistance while solidifying the client experience resulting in referrals. Strong communication and in...
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Clinical Data Coordinator
$49,392.00 - $132,000.00
Typical Salary for Clinical Data Coordinator in Bridgewater
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Data Coordinator
Supports clinical studies by maintaining a document management and control system.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Data Center Experience
Help Authoring Tools
Determines document control requirements by studying protocols, policies, and standard operating procedures (SOPs).
Enhances department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
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