PHARMAFull-time
Senior CDA/ Clin Data Assoc II
By Admin · Clinical Data Management
BANGALORE (IN)HYBRIDPOSTED: 9/13/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE OVERVIEW
Perform clinical data management and data cleaning activities for clinical trials while ensuring compliance with GCP, SOPs and client requirements, with responsibility for specialized processes and support to junior staff.
ROLE DEFINITION & RESPONSIBILITIES
- •Support database design, testing of data entry screens and DVM creation
- •Review clinical data listings for accuracy and consistency
- •Act as subject matter expert for specialized study-specific processes
- •Generate, track and resolve data clarifications and queries
- •Make required changes to clinical databases
- •Produce project-specific status reports for management and clients
- •Contribute to global data management process improvements
- •Provide training and work direction to junior staff
Reporting Hierarchy: Works within the Clinical Research/PPD clinical research services organization; Provides project-specific reporting to management and/or clients; Collaborates with clinical research and data management stakeholders and may provide direction to junior staff
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree or equivalent relevant academic/vocational qualification
- 3-7 years of comparable relevant experience
- Knowledge of medical and clinical terminology
- Understanding of study protocols and DVM
- Ability to meet applicable DM technical competencies
PREFERRED QUALIFICATIONS
- •Clinical data management experience in CRO or pharmaceutical environments
- •Experience with clinical database setup and data validation
- •Experience with GCP and global SOPs
- •Experience providing training or work direction to junior staff
REQUIRED VERIFIED SKILLS
Clinical data management
clinical data cleaning
database design
data validation
DVM
data review
query management
GCP
SOP compliance
clinical terminology
analytical problem-solving
project reporting
stakeholder communication
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Collaboration and professional development opportunities; exposure to global clinical research projects; opportunities to contribute to process improvement and scientific excellence
The posting does not disclose a salary range or bonus/equity amount; compensation should therefore be treated as undisclosed.
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global scientific and healthcare company whose PPD clinical research services organization supports pharmaceutical and biotechnology companies in clinical development.
TEAM SIZE: 120,000+ employees
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
Culture: Culture emphasizes scientific excellence, innovation, collaboration, development, customer focus and meaningful contributions to healthcare breakthroughs.
EXPECTED CAREER ROADMAP
Potential progression into Clinical Data Manager, Lead Clinical Data Associate, Clinical Data Management Project Lead or broader clinical research operations roles.
APPLICATION ADVISORY
Emphasize 3-7 years of clinical data management experience; highlight GCP/SOP compliance and clinical data cleaning; demonstrate database setup, DVM and query-management experience; mention clinical terminology and protocol knowledge; showcase process-improvement contributions and experience mentoring junior staff.
RECOMMENDED TRAINING
1/5
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