Job Description
A world-renowned pharmaceutical company is looking for a strong Clinical Data Documentation Specialist to support the lab in New Haven, CT. This person will be responsible for formatting, transfers, and archives both clinical biomarker test results and study documents in support of Pfizer clinical trials documentation
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Skills and Requirements
2-4 years work experience in biotechnology or pharmaceutical industry with demonstrated ability in the management of digital data or document information and workflowsWork experience in a regulated lab or quality assurance department preferred
knowledgeable of good documentation practices
Advanced proficiency in Microsoft Excel, Word, and Teams
Familiarity with file and data management tools, e.g. IDBS E-workbook, Veeva Vault, Generis CARA
Detail-oriented with ability to learn new processes and systems quickly
Positive attitude with a desire to learn and contribute to large team projects that occasionally require flexible working hours
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