Clinical Data Svs Associate

HypTechie; Bengaluru; On-site; INR 600,000 - 800,000; Full time

Job summary

HypTechie is hiring a Clinical Data Svs Associate to support our Life Sciences R&D vertical in Bengaluru. The role focuses on clinical data management activities, including discrepancy review, query resolution, and database validation.

You will design, test, and validate EDC systems, create UAT procedures, and ensure data quality for research and regulatory readiness. You will work in a team environment with cross-functional stakeholders, contribute to test plans and scripts, and help manage

Qualifications

• BE/MSc in a relevant field
• Experience in clinical data testing and database validation
• Ability to design and execute EDC test plans and scripts
• Knowledge of UAT procedures for EDC systems

Responsibilities

• Design and test EDC databases and CRFs
• Create and maintain UAT procedures for EDC systems
• Perform discrepancy review, query generation and resolution
• Lead or contribute to data verification and validation activities
• Coordinate with cross-functional teams in R&D and QA

Skills

Clinical Database Testing

Performance Testing Strategy

Automated Testing

Stakeholder management

Ability to perform under pressure

Agility for quick learning

Education

BE

MSc

Job description

Job description

Skill required:Clinical Data Operations – Clinical Database Testing

Designation:Clinical Data Svs Associate

Qualifications:BE/MSc

Years of Experience:1 to 3 years

What would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings – Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports.

What are we looking for?

• Clinical Database Testing
• Performance Testing Strategy
• Automated Testing
• Ability to manage multiple stakeholders
• Ability to perform under pressure
• Agility for quick learningRoles and Responsibilities:
• In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
• Your expected interactions are within your own team and direct supervisor
• You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
• The decisions that you make would impact your own work
• You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
• Please note that this role may require you to work in rotational shiftsQualificationBE,MSc

Role:Clinical research Scientist
Industry Type:IT Services & Consulting
Department:Research & Development
Employment Type:Full Time, Permanent
Role Category:Pharmaceutical & Biotechnology
Education
UG:Any Graduate
PG:Any Postgraduate