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Study Coordinator (Remote – Tamil & English)

Propharma
2+ years
3 LPA - 6 LPA
Remote, India, India
1 June 30, 2026
Job Description
Job Type: Contract Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Study Coordinator (Remote – Tamil & English)

Company: ProPharma
Location: India (Remote)
Department: Clinical Research Operations
Job Type: Part-Time (10 Hours/Week)
Work Mode: Remote
Contract Duration: 1-Year Fixed Term (Extendable up to 3 Years)

JOB OVERVIEW

The Study Coordinator is responsible for coordinating day-to-day clinical trial activities at investigator sites, supporting patient recruitment, study documentation, clinical data management, protocol execution, and regulatory compliance. The role involves site communication, subject coordination, informed consent management, medical record collection, data entry, query resolution, study closeout support, and ensuring compliance with ICH-GCP, IRB, FDA, and company Standard Operating Procedures (SOPs). This position requires fluency in both Tamil and English and the ability to work independently in a remote clinical research environment.


KEY RESPONSIBILITIES

Clinical Trial Coordination

  • Coordinate day-to-day clinical trial activities at assigned sites.

  • Serve as the primary point of contact for site communications.

  • Coordinate study-related activities with investigators and study teams.

  • Support study execution according to protocol requirements.

  • Assist with study closeout activities.

Patient Recruitment & Screening

  • Support pre-screening and patient screening activities.

  • Coordinate participant recruitment activities.

  • Assist with subject enrollment and eligibility verification.

  • Schedule participant visits and study appointments.

  • Maintain participant tracking records.

Subject Management

  • Coordinate subject re-consenting activities.

  • Collect and manage participant medical records.

  • Assist the Principal Investigator with protocol-specific activities.

  • Ensure participant confidentiality and data privacy.

  • Maintain participant documentation throughout the study.

Clinical Data Management

  • Perform accurate clinical data entry.

  • Monitor clinical databases for assigned studies.

  • Evaluate and respond to system-generated queries.

  • Maintain data accuracy and completeness.

  • Support timely resolution of data discrepancies.

Site Communication

  • Maintain regular communication with investigator sites.

  • Coordinate document submissions and study updates.

  • Respond to site-related inquiries promptly.

  • Facilitate communication between study teams and sites.

  • Maintain communication records and documentation.

Regulatory & Documentation

  • Maintain study documentation in compliance with IRB and FDA requirements.

  • Ensure compliance with ICH-GCP guidelines.

  • Follow company Standard Operating Procedures (SOPs).

  • Maintain audit-ready study files.

  • Support regulatory documentation and inspections.

Technology & Remote Operations

  • Utilize web-based clinical research platforms.

  • Manage study activities using Microsoft-based systems.

  • Maintain secure remote working practices.

  • Support electronic clinical documentation processes.

  • Ensure privacy and confidentiality in the remote work environment.


EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Life Sciences

  • Pharmacy

  • Nursing

  • Biotechnology

  • Clinical Research

  • Healthcare

  • Or an equivalent qualification

Alternative Qualification

Minimum 2 years of combined education, knowledge, and relevant experience sufficient to perform the role.


EXPERIENCE REQUIREMENTS

Required

  • Minimum 2 years of experience as a:

    • Study Coordinator

    • Clinical Research Coordinator (CRC)

    • Clinical Trial Coordinator

Required Language Skills

  • Fluent in Tamil

  • Fluent in English

Preferred

  • Experience working with clinical study teams.

  • Experience supporting remote clinical trials.

  • Knowledge of IRB and FDA regulations.

  • Experience with electronic clinical databases.

  • Experience in CRO or pharmaceutical clinical research.