Clinical Data Associate

Fusion Market Research; Pune District, Ahmedabad District, Bengaluru; On-site; INR 250,000 - 360,000; Full time

Job summary

Fusion Market Research in Pune, India seeks a data-driven clinical data entry assistant to manage trial data. You will collect, review, and enter data into EDC systems, identify data issues, and support query generation to ensure accuracy.

You will also help with data cleaning, discrepancy resolution, and maintain documentation per SOPs and GCP while ensuring confidentiality and timeliness.

Qualifications

• Bachelor’s/Master’s in pharmacy, life sciences, or related field.
• Basic computer skills including MS Excel and MS Office.
• Strong attention to detail and data accuracy.

Responsibilities

• Assist in collecting, reviewing, and maintaining clinical trial data for accuracy and completeness.
• Perform clinical data entry and verification using Electronic Data Capture (EDC) systems.
• Identify missing, inconsistent, or incorrect data and assist in raising data queries.
• Support clinical data cleaning and discrepancy resolution as per study protocols.
• Maintain clinical trial documentation in accordance with SOPs and Good Clinical Practice (GCP) guidelines.
• Ensure data confidentiality and compliance with applicable clinical research requirements.
• Coordinate with clinical research teams to resolve data-related issues.
• Assist with database quality checks and routine data management activities.
• Maintain accurate records and meet assigned timelines while following quality standards.

Skills

Attention to detail

Analytical thinking

Data accuracy

Education

B.Pharm, M.Pharm, B.Sc., M.Sc., Biotechnology, Microbiology, Life Sciences, or other relevant healthcare qualifications

Tools

MS Excel

MS Office

Job description

Role & responsibilities

• Assist in collecting, reviewing, and maintaining clinical trial data for accuracy and completeness.
• Perform clinical data entry and verification using Electronic Data Capture (EDC) systems.
• Identify missing, inconsistent, or incorrect data and assist in raising data queries.
• Support clinical data cleaning and discrepancy resolution as per study protocols.
• Maintain clinical trial documentation in accordance with Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Ensure data confidentiality and compliance with applicable clinical research requirements.
• Coordinate with clinical research teams to resolve data-related issues.
• Assist with database quality checks and routine data management activities.
• Maintain accurate records and meet assigned timelines while following quality standards.

Preferred candidate profile

• B.Pharm, M.Pharm, B.Sc., M.Sc., Biotechnology, Microbiology, Life Sciences, or other relevant healthcare qualifications.
• Basic computer skills, including MS Excel and MS Office.
• Strong attention to detail, analytical thinking, and data accuracy.