US-Maryland-Rockville:Research Associate - Clinical Research
To apply for this position, please visit this Website. http://biotech.fyicenter.com/jobs/99886758_Research_Associate___Clinical_Research.html
Date: 13-Aug-2015
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Research Associate - Clinical Research

Responsibilities

Develops client materials according to project requirements. Monitors project changes to ensure documentation and software conforms to new requirements. Produces project-specific documentation, operating procedures, standards, and work flows with minimal
supervision. Supports data management activities. Works with clients and internal subject matter experts to develop software specifications. Documents specifications and obtains approvals. Evaluates software specifications, writes, and executes test
scripts to verify software meets specifications. Processes incoming and outgoing project materials. Monitors, verifies, and tracks receipt of documentation and ensures appropriate distribution of materials to internal and external research personnel and
sites. Prepares general correspondence, agendas and meeting minutes, reports, and other project-specific documentation. Ensures review, approval, and distribution to internal staff and external project participants. Designs, builds, and updates
spreadsheets and other tracking tools. Identifies and investigates problems and recommends and implements corrective action. Maintains clinical research records and related documents. Coordinates the activities of smaller, well-defined projects including
coordinating data safety monitoring boards. Reports status of activities and problems to operations and project managers as appropriate. Complies with company policies, procedures, and standards. Ensures work is completed on time and is of the highest
quality possible. Performs related duties as assigned.

Bachelor's degree in science, health, or related field. Masters degree preferred. Two-Five years of relevant experience. Previous experience with a pharmaceutical company, CRO, or with NIH is desirable. Familiarity with FDA and GCP regulations desirable.
Knowledge of Microsoft Office tools such as Word, Excel, and PowerPoint. Experience using data management systems preferred. Excellent written and verbal communication skills. Good analytical and problem solving skills. Detail-oriented.


Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/

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