Clinical Data Coordinator

Inductive Quotient Analytics; Hyderabad; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Inductive Quotient Analytics in Hyderabad is seeking a Clinical Data Management professional with at least 2 years of experience in clinical trial data activities. You will perform end-to-end clinical data management activities, ensuring high-quality databases in compliance with regulations.

The ideal candidate should have strong knowledge of Clinical Data Management processes and experience with EDC systems like Medidata Rave. This full-time position offers the opportunity to work with a team focused on healthcare transformation.

Qualifications

• 2+ years of relevant Clinical Data Management experience.

Responsibilities

• Perform end-to-end clinical data management activities for clinical trials.
• Review CRFs/eCRFs and ensure accurate data collection and validation.
• Generate, review, and resolve data queries with investigative sites.
• Perform data cleaning, discrepancy management, and reconciliation activities.
• Validate clinical data for completeness, consistency, and compliance.
• Coordinate with cross-functional teams including Clinical Operations, Biostatistics, and Programming teams.
• Support database lock activities and study closeout processes.
• Ensure compliance with CDISC, GCP, SOPs, and regulatory guidelines.
• Prepare and maintain study documentation and data management reports.
• Participate in UAT testing and review edit checks as required.

Skills

Strong knowledge of Clinical Data Management processes

Experience with EDC systems (Medidata Rave, Oracle Clinical, Inform, Veeva)

Knowledge of CRF review, query management, and data validation

Understanding of ICH-GCP and clinical trial processes

Good communication and coordination skills

Proficiency in MS Excel and clinical databases

Education

Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology or related field

Job description

Clinical Data Management (CDM) – Executive/Associate

About Us

Inductive Quotient was founded by statisticians and technology industry experts with over 20 years of experience. Inductive quotient aims to transform businesses and processes with their advanced digitization capabilities. With advanced AI and Machine Learning techniques we are helping Life Sciences industry to create a better healthcare system and our Data Science capabilities helps organizations to create breakthrough solutions to transform businesses and drive sales growth.

Website: www.inductivequotient.com

Why Inductive Quotient?

We are a team of 100+ talented and passionate professionals with a strong statistical and analytical background combined with required study expertise. We IQians take lots of pride in our culture that enables open and creative thinking, deeply valuing our employees and their contributions towards our organization success.

Experience: 2 Years

Employment Type: Full-Time

Job Summary

We are looking for a Clinical Data Management professional with 2+ years of experience in handling clinical trial data activities. The candidate will be responsible for data review, validation, query management, and ensuring high-quality clinical databases in compliance with regulatory and sponsor requirements.

Key Responsibilities

• Perform end-to-end clinical data management activities for clinical trials.
• Review CRFs/eCRFs and ensure accurate data collection and validation.
• Generate, review, and resolve data queries with investigative sites.
• Perform data cleaning, discrepancy management, and reconciliation activities.
• Validate clinical data for completeness, consistency, and compliance.
• Coordinate with cross-functional teams including Clinical Operations, Biostatistics, and Programming teams.
• Support database lock activities and study closeout processes.
• Ensure compliance with CDISC, GCP, SOPs, and regulatory guidelines.
• Prepare and maintain study documentation and data management reports.
• Participate in UAT testing and review edit checks as required.

Required Skills

• Strong knowledge of Clinical Data Management processes.
• Experience with EDC systems such as Medidata Rave, Oracle Clinical, Inform, or Veeva.
• Knowledge of CRF review, query management, and data validation.
• Understanding ICH-GCP and clinical trial processes.
• Good communication and coordination skills.
• Proficiency in MS Excel and clinical databases.

Qualification

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.
• 2+ years of relevant Clinical Data Management experience.

Preferred Skills

• Basic knowledge of CDISC standards.
• Exposure to SAE reconciliation and medical coding is an advantage.
• Ability to work in a fast‑paced and team-oriented environment.