Serves as the primary point of contact with clients / accounts assigned to Director, primarily in the New York/Mid-Atlantic area. Actively identifies, qualifies and continually promotes WCCT services in order to achieve annual sales objectives. Seeks out new business and new clients within assigned territory, therapeutic area, or Trial Phase.
Duties and Responsibilities, include but not limited to:
Achieve annual sales targets
Achieve number of expected client interactions
Maintain proper ...
The Contract Manufacturing Associate is responsible for maintaining stability data in the regulated systems, organizing records and creating databases to track manufacturing parameters. This individual is responsible for assisting with vendor relationship management, new vendor evaluation, and resolution of any technical and quality issues that may occur during manufacturing campaigns. The Contract Manufacturing Associate interacts with the Research and Development, Regulatory Affairs, Technical ...
The Associate Director/Director will serve as the principal HEOR strategist for the Therapeutic Area or Product and will report to the HEOR Functional Head. The Associate Director/Director will formulate and execute HEOR strategies and plans on behalf of the Functional Head.
• Develop and execute global and regional HEOR strategies and programs for Regeneron products, with aim to inform, support and strengthen commercialization activities, including marketing, ...
Head of Preclinical Development and Toxicology with a strong toxicology and immunotoxicity background w/ Experience with pharmacokinetics also desired. Direct experience designing and managing animal toxicology studies and other safety studies, and managing external CROs, as well as other IND enabling activities, including generating reports for FDA submission.
Primary responsibilities include all aspects of Preclinical Development including the design, development and direction of toxicology, ...
PRINCIPAL SAS PROGRAMMER-Work from Home!
*These remote opportunities are open to any US home-office location.
My client is seeking Principal SAS Programmers for full-time positions supporting our sponsor's biometrics project needs. In this role, the Principal SAS Programmer will serve as a lead programmer for projects; serve as contact with clients for programming aspects of clinical studies; and manage Biometrics teams for projects.
The selected candidate will be responsible for the following:
Below is a template job description. Every clients job description is a little different.
Duties and Responsibilities:
1. If job assignment includes tissue culture: Using SOPs, accurately and efficiently performs tissue culture of assigned specimen types, including culture initiation, maintenance, and harvest. Also performs slide preparation and staining for microscopic analysis.
2. If job assignment includes microscopic analysis:
Performs accurate microscopic/post-microscopic analyses of ...
Senior Regional Clinical Research Associate
Identifies potential investigators, contract research organizations and outside vendors. Collects required documentation for review by Project Manager to make a selection decision.
Conducts site visits pre-study, at study initiation, at regular intervals during the study and at study closeout.
Prepares a variety of reports and letters in accordance with study SOPs and industry standards.
Collects, reviews and processes regulatory documents. Ensures ...
MSN's client is seeking a Clinical Research Coordinator for their New York territory. The CRC is responsible for supporting clinical research staff and managing new and ongoing clinical research activities. The position includes assisting clinical investigators and research staff to drive projects forward by interacting closely with external clinical research organizations and sponsors. The CRC will adhere to GCP, ICH, and FDA guidelines in the conduct of all study related activities.
Duties and ...
Location - Can be located home based anywhere in the North East from DC on up next to a major airport. Travel will be throughout the North East region
Experience monitoring or coordinating cardiology clinical trails
At least two years or more monitoring clinical trials as a CRA - please do not apply unless you have clinical trial monitoring experience as a CRA
Bachelor’s degree in life sciences or related field or certification in a related allied health profession ...
Jun 26 -
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