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Clinical Documentation Specialist

Job

Insight Global

New Haven, CT (In Person)

Full-Time

Posted 2 weeks ago (Updated 3 days ago) • Actively hiring

Expires 7/10/2026

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Job Description

Job Description A world-renowned pharmaceutical company is looking for a strong Clinical 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 We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.

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Insight Global's Workforce Privacy Policy:
https://insightglobal.com/workforce-privacy-policy/. Skills and Requirements 2-4 years work experience in biotechnology or pharmaceutical industry with demonstrated ability in the management of document information and workflows Work experience in a regulated lab or quality assurance department preferred knowledgeable of good documentation practices Advanced proficiency in Microsoft Excel, Word, and Teams Transfer signed study documents to long-term archival and link to trial master files when appropriate Communicate openly with internal Biomarker Lab Head and Project Leads and with external Biomarker Clinical Assay Leads and master file owners All deliverables adhere to agreed upon timelines Attend biweekly Biomarker Study Management Meetings and monthly Clinical Bioanalytic Meetings Positive attitude with a desire to learn and contribute to large team projects that occasionally require flexible working hours