Syngene International is hiring a Data Entry Operator – Clinical Data Management (CDM) in Bangalore for its Translational & Clinical Research (T&CR) department. The position is suitable for freshers and candidates with up to 2 years of experience in clinical data management, clinical research, healthcare, life sciences, pharmacy, biotechnology, or related disciplines.
The role focuses on accurate clinical data entry, CRF and DCF management, data quality checks, documentation, query coordination, and clinical study records. Candidates with knowledge of Clinical Research Forms (CRFs), source documents, GCP, data entry, and clinical research documentation can consider this opportunity.
Syngene Data Entry Operator – CDM Job Details
| Particular | Details |
|---|---|
| Company | Syngene International Limited |
| Job Title | Data Entry Operator |
| Department | Clinical Data Management – T&CR |
| Job Location | Bangalore, Karnataka |
| Experience | Fresher to 2 years |
| Employment Type | Full-time |
| Qualification | Bachelor’s or Master’s degree |
| Eligible Fields | Life Sciences, Pharmacy, Biotechnology, Clinical Research, Health Sciences or related disciplines |
| Salary | Not disclosed by the employer |
| Job Posted | September 21, 2026 |
| Industry | Clinical Research / Life Sciences / CRO |
About Syngene International
Syngene International is an innovation-led contract research, development and manufacturing organization providing scientific services across areas including early discovery, development and commercial supply.
The company emphasizes safety, quality, integrity, compliance and operational discipline across its activities.
Job Responsibilities
The selected candidate will support clinical data management and documentation activities associated with clinical studies.
Key Data Entry Operator – CDM responsibilities include:
- Receive, track and maintain Case Report Forms (CRFs) and Data Clarification Forms (DCFs).
- Perform accurate and timely clinical data entry into designated data capture systems.
- Maintain records related to CRF and DCF receipt, processing, retrieval and storage.
- Conduct routine data quality reviews to identify missing information, discrepancies and data entry errors.
- Support query generation and resolution by coordinating with relevant stakeholders.
- Process scanned CRFs in accordance with applicable eCTD requirements, including bookmarking, indexing and Table of Contents creation.
- Prepare and maintain source CRF documents for BA/BE and Phase I studies.
- Maintain the accuracy, completeness and confidentiality of clinical trial data.
- Maintain study documentation, logs and records according to SOPs, GCP requirements and applicable regulations.
- Support document filing, archiving and retrieval throughout the study lifecycle.
- Assist with study startup, study conduct and closeout activities related to clinical data handling.
- Work with clinical data management, clinical operations and quality teams to support study deliverables.
- Participate in process improvement initiatives focused on data quality and operational efficiency.
- Support audits, inspections and quality assessments by providing required documentation.
- Follow organizational safety, quality and data-integrity requirements.
Syngene Data Entry Operator Eligibility
Candidates should meet the following requirements:
Educational Qualification
Applicants should have a Bachelor’s or Master’s degree in one of the following areas:
- Life Sciences
- Pharmacy
- Biotechnology
- Clinical Research
- Health Sciences
- Related disciplines
Degrees such as B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotechnology and Clinical Research-related qualifications may be relevant where they align with the employer’s stated disciplines.
Experience
The position is open to:
- Freshers
- Candidates with up to 2 years of relevant experience
- Candidates with internship, academic project or training experience in clinical research or clinical data management
Required Skills
Candidates interested in this Clinical Data Management job in Bangalore should ideally have:
- Basic knowledge of clinical research processes.
- Understanding of Clinical Data Management (CDM).
- Familiarity with CRFs and source documents.
- Understanding of clinical data entry procedures.
- Strong attention to detail.
- Ability to identify discrepancies and perform data verification.
- Basic MS Office proficiency.
- Familiarity with data capture systems is advantageous.
- Basic understanding of Good Clinical Practice (GCP).
- Knowledge of data confidentiality and regulatory compliance.
- Strong documentation and organizational skills.
- Good communication and teamwork abilities.
- Ability to manage multiple tasks within defined timelines.
- A quality-focused and accountable approach to work.
Who Can Apply?
This Syngene Data Entry Operator vacancy may be relevant for fresh graduates and early-career professionals from life-science and healthcare backgrounds.
Potentially relevant qualifications include:
B.Pharm | M.Pharm | Pharm.D | B.Sc | M.Sc | Biotechnology | Clinical Research | Health Sciences | Life Sciences
Candidates with internships or academic projects involving clinical research, clinical data management, CRFs, clinical trial documentation or healthcare data may have an additional advantage.
Career Opportunity in Clinical Data Management
Clinical Data Management is an important function within clinical research because clinical study information must be collected, reviewed, documented and maintained accurately throughout the study lifecycle.
A Data Entry Operator working within CDM can gain exposure to areas such as:
- Clinical trial data entry
- Case Report Forms
- Data Clarification Forms
- Data quality review
- Query management
- Clinical documentation
- GCP compliance
- Study startup and closeout
- Clinical research systems
- Data integrity and documentation practices
For graduates looking to establish a career in Clinical Data Management, Clinical Research or the CRO industry, this type of position can provide practical exposure to clinical study operations.
How to Apply
