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The Trade Promotions Manager will be responsible for developing & implementing the trade promotion plan, strategy, tactics, funding, assortment, analysis and communication for the respective business unit and category that is consistent with brand strategy. Key responsibilities include, but are not limited to Managing the trade promotional budget for business unit and ensuring appropriate reso
Posted Today
Review of protocols, test samples, inclusion/exclusion criteria, recruitment requirements and study schedule. Implementation of all aspects of clinical trials, including compliance to Standard Operating Procedures, IRB approved protocols, Human Subject Protection, and regulatory requirements. Perform CRF transcription and data entry into Excel or EDC platform. Peer review clinical trial data as
Posted 1 day ago
The Clinical Trial Technician position is based within our Clinical Patch Testing department, and works with departmental management and the Principal Investigator in the implementation of clinical trials for patch testing protocols. Job Type Part Time. Base Hours 7 00AM – 11 00AM and/or 4 00PM 8 00PM Monday, Wednesday and Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an
Posted 9 days ago
Seeking individual for media prep/technician position in our Fairfield, NJ facility. CPTC provides testing and consultation services to the pharmaceutical, cosmetic, personal care, medical device and household product industries. Job Type Full Time. Base Hours 8 00AM – 5 00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be able to perfor
Posted 9 days ago
Seeking individual for senior analyst position in our Fairfield, NJ facility. CPTC provides testing and consultation services to the pharmaceutical, cosmetic, personal care, medical device and household product industries. Job Type Full Time. Base Hours 8 00AM – 5 00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job successfully, an individual must be able to
Posted 9 days ago
Review database for panelists with matching inclusion/exclusion criteria to upcoming clinical trial protocols. Contact potential subjects and discuss clinical trial requirements and availability to participate Ensure compliance with protocols, and standard operating procedures Data entry of subject data into database Provide assistance to clinical and photobiology departments as needed EDUCATION
Posted 9 days ago
Review laboratory testing records for accuracy, completeness and compliance with GMP, GLP, GCP regulations and internal procedures. Assist in conducting investigations and other Quality Management System activities. Work collaboratively and effectively with other QA Team members and the technical staff. EDUCATION and/or EXPERIENCE Minimum HS diploma; Associate’s degree or higher preferre
Posted 22 days ago
Responsible for receiving and documenting sample log in. This includes all of the following Document the receipt of samples for analysis into the laboratory Prepare study folders Perform accurate labeling of samples Update and maintain study folder revisions Serve as client contact with regard to completion of authorizing documentation Ability to work independently and as part of a team Perfor
Posted 1 month ago
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