Clinical Documentation Specialist (2nd Shift)

Syneos Health, Inc.

Indiana (PA)

On-site

USD 42,000 - 62,000

Full time

6 days ago
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Job summary

Syneos Health, Inc. is seeking a Clinical Document Agent for the 2nd shift (2 PM to 11 PM IST). The role requires creating documentation forms, drafting patient files, and converting data into electronic formats while adhering to established procedures.

You will support clinical studies and collaborate with global teams to ensure timely delivery. The candidate should have a Life Sciences degree and 1–3 years of related experience, with strong Excel and Word skills and knowledge of ISF and Phase

Qualifications

  • Bachelor or Master’s degree in Life Sciences.
  • 1–3 years of experience in clinical data management or related field.
  • 2 PM–11 PM IST shift experience or readiness to work this window.
  • Understanding of Clinical Trial documentation and ISF.
  • Phase 1 experience is must.
  • Must have experience in Document QC and Excel form creation.
  • Strong communication and ability to coordinate with cross-functional global teams.

Responsibilities

  • Create documentation forms for clinical projects and draft patient files.
  • Convert raw data to electronic formats following SOPs.
  • Prepare subject files, templates, and timelines, with client feedback incorporated.
  • Digitalize raw data transferred by the Clinical Study Manager.
  • Perform peer review of team work and assist in training new members.
  • Collaborate with internal and external stakeholders to obtain necessary documents.

Skills

Excellent communication
Cross-functional teamwork
Attention to detail

Education

Bachelor / Master’s degree in Life Sciences

Tools

Microsoft Word
Microsoft Excel
Adobe Acrobat

Job description

Syneos Health, Inc. is seeking a Clinical Document Agent for the 2nd shift (2 PM to 11 PM IST). The role requires creating documentation forms, drafting patient files, and converting data into electronic formats while adhering to established procedures.

You will support clinical studies and collaborate with global teams to ensure timely delivery. The candidate should have a Life Sciences degree and 1–3 years of related experience, with strong Excel and Word skills and knowledge of ISF and Phase

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