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Syneos Health Hiring for Clinical Document Agent | Remote

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Syneos Health

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences or Relevant

Remote

1–3 Years

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Syneos Health Hiring for Clinical Document Agent | 1–3 Years | Remote

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Syneos Health is hiring for the position of Clinical Document Agent for its Research & Development team. The role offers a remote work opportunity, with the hiring office located in Hyderabad.

The position is suitable for candidates with experience in clinical trial documentation, Phase 1 clinical trials, Investigator Site Files (ISF), document quality control, Excel-based documentation, and Adobe tools.

Job Details

DetailsInformation
CompanySyneos Health
PositionClinical Document Agent
Experience1–3 Years
Work ModeRemote
Hiring OfficeHyderabad
Openings2
Employment TypeFull Time, Permanent
DepartmentResearch & Development
IndustryPharmaceutical & Life Sciences

Key Responsibilities

  • Manage and maintain clinical trial documentation.
  • Apply knowledge of Phase 1 clinical trial documentation.
  • Work with Investigator Site Files (ISF) and related documentation.
  • Perform document quality control (QC) activities.
  • Create forms and source documentation using Microsoft Excel.
  • Use Excel to develop and manage clinical documentation.
  • Work with Adobe and other computer-based documentation tools.
  • Understand project requirements and translate them into appropriate documentation.
  • Coordinate with cross-functional and global teams.
  • Communicate effectively with stakeholders involved in clinical documentation activities.

Required Skills

Candidates should have experience or knowledge in:

  • Clinical Trial Documentation
  • Phase 1 Clinical Trials
  • Investigator Site Files (ISF)
  • Document Quality Control
  • Microsoft Excel
  • Form & Source Documentation Creation
  • Adobe
  • Clinical Research
  • Cross-functional Coordination
  • Global Team Collaboration
  • Communication Skills

Educational Qualification

Undergraduate:

  • B.Sc. in any specialization
  • B.Pharm in any specialization

Postgraduate:

  • M.Sc./MS in Science
  • M.Pharm

Who Can Apply?

Candidates with 1–3 years of relevant experience in clinical documentation, clinical research, or related pharmaceutical/life sciences functions can consider this opportunity.

Experience with Phase 1 clinical trials and document QC is specifically required for the role.

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