Clinical Data Management Associate
Location: Bengaluru, India
Job Type: Full-Time
Work Mode: Hybrid
Reference ID: R1525503
Industry: Clinical Research / CRO / Life Sciences
Job Overview
A leading global clinical research organization is seeking a Clinical Data Management (CDM) Associate to support the delivery of high-quality, accurate, and compliant clinical trial data.
This role contributes to efficient data management processes across clinical studies, ensuring that deliverables meet regulatory standards, sponsor expectations, and project timelines. The position may also involve limited leadership responsibilities under the supervision of a Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
This opportunity is ideal for professionals looking to build or advance their career in clinical data management within a hybrid working environment in Bengaluru.
Key Responsibilities
Clinical Data Management Operations
Provide data management support for assigned clinical protocols
Serve as Data Operations Coordinator (DOC) for:
One protocol with fewer than five operations staff (excluding Data Entry), or
15+ easy to moderately complex central laboratory studies
Act as backup to DOC or Data Team Lead (DTL) when required
Conduct data review and validation activities
Write, review, and resolve data clarification forms (DCFs)
Perform clinical data coding in accordance with study requirements
Database Development & Testing
Develop, review, and test clinical databases and edit check specifications
Perform user acceptance testing (UAT) and programming validation
Support database audit activities
Contribute as a coder, tester, or database designer (non-advanced programming environments)
Quality & Compliance
Ensure adherence to core operating procedures (SOPs) and working instructions
Maintain high standards of data accuracy, integrity, and regulatory compliance
Meet assigned study timelines and quality objectives
Maintain effective communication with CDM team members, sponsors, and stakeholders
Required Qualifications
Education
Bachelor’s Degree in Clinical, Biological, Mathematical Sciences, or a related field
OR
Equivalent combination of education, training, and relevant experience
Experience Required
1–3 years of experience in Clinical Data Management, Clinical Research, or related healthcare research environment preferred
Exposure to medical terminology required
Experience with clinical databases, edit checks, and data validation processes preferred
Prior experience in CRO or pharmaceutical clinical trials environment is an advantage
Core Skills & Competencies
Technical Skills
Clinical Data Management (CDM) processes
Data review and data cleaning
Database development and testing
Clinical data coding
Programming validation and UAT testing
Knowledge of clinical trial workflows
Familiarity with GCP and regulatory standards
Professional Skills
Strong attention to detail and data accuracy
Excellent organizational and time management skills
Strong written and verbal communication skills
Ability to work independently and proactively resolve issues
Collaborative mindset with ability to work in cross-functional teams
Strong computer proficiency and analytical capability
Why Apply
Work with a globally recognized clinical research organization
Gain exposure to international clinical trials and regulatory frameworks
Hybrid work model offering flexibility
Career progression opportunities in Clinical Data Management and Data Operations
Equal Opportunity & Recruitment Integrity
The organization is committed to integrity and transparency in hiring practices. All application information must be accurate and complete. Any misrepresentation during the recruitment process may result in disqualification or termination in accordance with applicable laws.
Equal employment opportunities are provided without discrimination based on race, gender, religion, national origin, disability, or other protected status.
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