Novotech Clinical Data Associate Jobs

Pharma Hiring Hub; Bengaluru; On-site; INR 420,000 - 640,000; Full time

Job summary

Novotech is seeking a Clinical Data Associate I in Bengaluru to join the Clinical Data Management team. The role targets candidates with 6 months to 1 year of experience or fresh graduates with relevant internships in CDM.

You will handle data validation, CRF review, data listing generation, and assist in EDC setup while ensuring adherence to ICH-GCP and related standards.

Qualifications

• Experience or training in Clinical Data Management (CDM) and regulatory standards.
• Familiarity with EDC platforms and data listing generation.
• Knowledge of ICH-GCP and data integrity requirements.

Responsibilities

• Validate clinical data for accuracy and completeness.
• Review and resolve data queries and discrepancies.
• Track CRFs and maintain study documentation.
• Support database setup and user acceptance testing.
• Perform data reconciliation with external lab data.
• Generate study reports and data listings.
• Coordinate medical coding using MedDRA and WHO Drug Dictionary.
• Participate in project meetings and maintain documentation.
• Ensure compliance with ICH-GCP, GCDMP, and SOPs.

Skills

CDM fundamentals

EDC systems

CRF review

Database validation

Medidata Rave

ICH-GCP knowledge

Communication

Analytical thinking

Education

B.Pharm

M.Pharm

Pharm.D

B.Sc

M.Sc

Biotechnology

Microbiology

Nursing

Clinical Research

Allied Health Sciences

Tools

Medidata Rave

Oracle InForm

Job description

Clinical Data Management (CDM) has become one of the most promising career paths for pharmacy and life sciences graduates who want to work in the clinical research industry. Every clinical trial generates thousands of data points that must be collected, verified, validated, and maintained before regulatory authorities can evaluate the safety and effectiveness of a new medicine. Clinical Data Associates play a critical role in ensuring this information is accurate, complete, and compliant with international quality standards.

Novotech, a globally recognized Contract Research Organization (CRO), has announced an exciting opportunity for the position of Clinical Data Associate I at its Bangalore office. This role is ideal for candidates with six months to one year of experience, while fresh graduates with relevant internships or Clinical Data Management training may also have a good opportunity to apply.

If you are planning to build a long-term career in Clinical Data Management, Clinical Research, or Clinical Trial Operations, this opportunity can provide valuable exposure to international clinical studies, electronic data capture systems, and regulatory-compliant data management processes.

Job Overview

Particulars

Details

Company Novotech

Position Clinical Data Associate I

Job ID 4127

Location Bangalore, Karnataka

Department Clinical Data Management

Employment Type Full-Time

Experience 6 Months – 1 Year Preferred

Qualification B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotechnology, Nursing & Life Sciences

Last Date 2 July 2026

About Novotech

Novotech is a leading global CRO that provides clinical research services to pharmaceutical, biotechnology, and medical device companies. With operations across Asia-Pacific, North America, and Europe, the organization supports sponsors throughout the clinical development process by delivering high-quality clinical operations, data management, biostatistics, regulatory support, and project management services.

Joining Novotech allows professionals to work on global clinical trials while learning international data standards, electronic data capture systems, and Good Clinical Practice (GCP) requirements.

The Clinical Data Associate I will support various Clinical Data Management activities while ensuring high standards of data quality and regulatory compliance throughout the clinical trial lifecycle.

• Validate clinical data for accuracy, completeness, and consistency.
• Review and resolve clinical data queries.
• Track Case Report Forms (CRFs) and maintain study documentation.
• Support database setup and user acceptance testing.
• Perform external laboratory data reconciliation.
• Generate study reports and clinical data listings.
• Coordinate medical coding activities using MedDRA and WHO Drug Dictionary.
• Participate in project meetings and maintain meeting documentation.
• Ensure compliance with ICH-GCP, GCDMP, and company SOPs.
• Support continuous process improvement initiatives.

Eligibility Criteria

• B.Pharm
• M.Pharm
• Pharm.D
• B.Sc
• M.Sc
• Biotechnology
• Microbiology
• Nursing
• Clinical Research
• Allied Health Sciences

Skills That Can Strengthen Your Profile

• Clinical Data Management fundamentals.
• Electronic Data Capture (EDC) systems.
• CRF review and query management.
• Database validation.
• Medidata Rave or Oracle InForm knowledge.
• ICH-GCP and GCDMP understanding.
• Communication and teamwork skills.
• Analytical thinking.

Why Join Novotech?

Working with Novotech offers excellent exposure to international clinical trials while providing structured career development opportunities for Clinical Data Management professionals.

• Global CRO experience.
• International clinical trial exposure.
• Flexible working environment.
• Learning and development programs.
• Career progression opportunities.
• Wellness and employee benefit programs.

Clinical Data Management professionals can build rewarding long-term careers by progressing into positions such as Clinical Data Coordinator, Clinical Data Manager, Lead Data Manager, Clinical Systems Specialist, Database Programmer, Clinical Project Manager, and Clinical Operations Manager. Experience with EDC platforms and global regulatory standards significantly enhances career prospects within CROs and pharmaceutical companies.

Resume Tips

• Mention any internship or training in Clinical Data Management.
• Highlight EDC systems such as Medidata Rave or Oracle InForm.
• Include knowledge of GCP and GCDMP.
• Showcase data entry, validation, or research projects.
• Keep your resume ATS-friendly and well-structured.