Clinical Data Associate I (CDA I)
Location: Remote, India
Job ID: R-01338259
Employment Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Standard (Monday to Friday)
About the Role
A leading global Contract Research Organization (CRO), supporting the PPD® clinical research portfolio, is seeking a Clinical Data Associate I (CDA I) to join its growing Clinical Data Management team in India. This entry-level role is ideal for professionals looking to build a strong foundation in clinical data management while contributing to global clinical trials that bring innovative therapies to patients worldwide.
The organization has supported over 2,700 clinical trials across 100+ countries and partners with the world’s top pharmaceutical and biotechnology companies to accelerate drug development and ensure data integrity.
Role Overview
The Clinical Data Associate I is responsible for performing entry-level clinical data cleaning and reconciliation activities with a high degree of accuracy and compliance. The role supports inspection-ready clinical data by adhering to GCP guidelines, global SOPs/WPDs, and study protocols, while working closely with cross-functional study teams throughout the clinical trial lifecycle.
Key Responsibilities
Identify, analyze, and resolve data discrepancies in clinical databases
Generate, track, and resolve data queries and data clarification forms (DCFs)
Perform updates and corrections in the data management database as required
Support clinical data cleaning and reconciliation activities in line with study timelines
Assist with CRF design and implementation using approved graphic design or EDC tools, as applicable
Ensure compliance with regulatory guidelines, SOPs, and client-specific requirements
Maintain confidentiality of clinical trial data and proprietary client information
Support inspection-readiness through accurate documentation and audit-compliant processes
Education Requirements
Bachelor’s degree or equivalent formal academic qualification in a relevant discipline
Experience Requirements
Minimum 1 to 1.6 years of experience in Clinical Data Management or a related clinical research role
Hands-on experience with RAVE (Medidata) and/or Veeva EDC is required
Required Skills and Competencies
Strong attention to detail with good numerical accuracy
Working knowledge of clinical trial protocols and Data Validation Manuals
Ability to work with interactive computer-based clinical systems
Good analytical and problem-solving skills
Strong written and verbal communication skills with a solid command of English
Ability to work effectively under direct supervision
Proven ability to work both independently and within a team environment
High standards of data confidentiality and ethical conduct
Demonstrated flexibility, adaptability, and sound judgment in decision-making
Working Conditions
Work is primarily performed in a remote office environment
Occasional travel to site locations may be required, depending on study needs
Career Growth and Development
This role supports a Functional Service Provider (FSP) model for a globally recognized biopharmaceutical sponsor known for innovation in specialty medicines, vaccines, and scientific research. As a client-dedicated FSP professional, you will collaborate with global data science and clinical teams on high-visibility studies within a mature, quality-driven delivery model.
The organization offers structured career development through:
Tailored learning pathways and role-based training
Mentorship and stretch assignments
Multiple career progression options, including Senior Clinical Data Management, Clinical Data Team Lead (CDTL), CDM Project Management, or transitions into Data Standards or Clinical Programming, based on performance and business needs
Why Join This Opportunity
Gain hands-on experience with modern Clinical Data Management systems and processes
Work on global clinical trials across multiple therapeutic areas and phases
Build expertise in EDC, data quality, reconciliation, and AI-enabled clinical trial workflows
Develop analytical, project management, and risk management capabilities in a global delivery environment
Contribute directly to bringing life-changing medicines to patients worldwide
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. The company’s mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, improving diagnostics, and delivering innovative pharmaceutical services through globally recognized brands.
Equal Employment Opportunity
The organization is an Equal Opportunity Employer and is committed to fostering a diverse, inclusive, and accessible workplace.
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