• Coordinate and deliver application development related activities. Lead a team of 3 – 5 team members to achieve success in design, development and deployment activities.
• Perform hands on development and coding of application components.
• Review technical deliverables created by other team members.
• Utilize an agile product engineering methodology while working collaboratively with a variety of product teams (data integration, quality assurance, configuration management, product management ...
• The CDS will support the Company’s regulatory function and study team in the document management of clinical research trials from the project development stage through to project completion. Mainly, the CDS will perform a variety of research, database, and administrative duties of a routine and technical nature in support of clinical trials to assist investigators in organizing, gathering, and compiling clinical research data.
DUTIES AND RESPONSIBILITIES:
• Assist with collecting, ...
• The Regulatory Affairs Specialist supports the Company’s regulatory function and project teams through the provision of a variety of administrative and technical tasks involving the management of clinical research trials documentation. In addition, the Regulatory Affairs Specialist performs a variety of research, database, and administrative duties of a routine and technical nature in support of corporate initiatives and clinical trials to assist MedSource and/or clients in organizing, ...
our client is in weston, MA seeking an experienced JAVA / J2ee developer with spring and hibernate experience. This is a long term consulting position. If interested, please apply to this ad
Job #: 13-01192
(must have a minimum of 5 years Java Development experience with Spring,Tiles, and Hibernate). Communication must be above average as the position will have direct partnership with the business partners.
The developer is to act as the technical lead for a large scale, FDA-regulated application ...
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