Clinical Documentation Specialist

Think-i

0 years

3 - 6 Lacs

bengaluru delhi / ncr mumbai (all areas)

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Skills Required

pharmaceutical life sciences drug regulatory affairs biotechnology medical records pharmacovigilance clinical trials ich clinical pharmacy clinical research drug safety healthcare medical affairs pharma clinical data management clinical documentation clinical data

Work Mode

Hybrid

Job Type

Full Time

Job Description

Role & responsibilities

Handle, organize, and maintain clinical, medical, and healthcare project documentation.
Accurately enter and validate healthcare and research data in internal systems.
Review medical case records, lab reports, and related documentation for completeness.
Collaborate with research, operations, and regulatory teams to gather required information.
Prepare, format, and update reports for ongoing research and healthcare projects.
Track timelines for documentation deliverables in line with project schedules.
Maintain data confidentiality and adhere to industry compliance standards.
Assist in the preparation of records for audits, inspections, and submissions.
Perform quality checks on all documentation for accuracy and completeness.
Support creation of summaries, logs, and data trackers for clinical projects.
Identify gaps in documentation and take corrective actions.
Contribute to continuous process improvement for document handling.

Fresher Hiring - Pharma / Life Sciences / Medical

Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates

Medical - BDS, BHMS, BAMS, MBBS

Location - All India - Delhi, Mumbai, Pune, Bangalore, Kochi, Chennai, Hyderabad, Ahmedabad, Bhopal, Indore, Kolkata, Chandigarh

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