Clinical Data Associate
📍 Location: India
🏢 Company: Novotech
Category: Clinical Data Management
Employment Type: Full-time
About the Role
The Clinical Data Associate (CDA) plays a key role in supporting the day-to-day operations of Clinical Data Management (CDM) projects.
This position provides data entry and administrative support to ensure accuracy, integrity, and timely delivery of clinical trial data, working closely with Clinical Data Managers (CDMs) and other stakeholders.
Key Responsibilities
Perform data entry of clinical trial data using Clinical Data Management software.
Assist in the review and resolution of data queries raised by sponsor companies or monitoring staff.
Track Case Report Form (CRF) pages received, entered, and data queries sent/received/entered.
Support database testing and edit check testing under the guidance of CDMs.
Assist in data cleaning, validation, and reconciliation of external data sources.
Maintain clear and effective communication with Lead CDMs and project teams.
Help create reports, listings, and data outputs as required throughout the project lifecycle.
Experience and Qualifications
Education: Graduate in Clinical, Life Sciences, or related field.
Relevant qualifications or experience in allied professions may also be considered.
Experience:
Preferably 6 months to 1 year of experience in Clinical Data Management, pharmaceutical research, or related industry roles.
Skills:
Strong attention to detail and accuracy.
Good communication and teamwork skills.
Familiarity with clinical data systems and standard data management procedures.
About Novotech
Novotech is a global full-service Clinical Research Organization (CRO) headquartered in Sydney, Australia, with 34 offices across Asia-Pacific, North America, and Europe.
Employs 3,000+ professionals and partners with 5,000+ clinical sites worldwide.
Offers full-spectrum clinical development services, including:
Feasibility assessments
Ethics and regulatory submissions
Data management and statistical analysis
Medical monitoring and safety solutions
Central lab services, report writing, project, and vendor management
Certified in ISO 27001 (Information Security) and ISO 9001 (Quality Management), reflecting commitment to world-class data security and quality standards.
Our Culture and Benefits
At Novotech, we are passionate about advancing healthcare and fostering a diverse, inclusive, and supportive workplace.
We offer:
Flexible working options and hybrid setups
Paid parental leave for both parents
Flexible leave entitlements and wellness programs
Continuous training and career development opportunities
A collaborative culture where every voice is heard and valued
We encourage applications from:
Candidates passionate about clinical research and biotech
Individuals who identify as LGBTIQ+, have a disability, or caring responsibilities
Novotech is a Circle Back Initiative Employer — we commit to responding to every application.
About the Team
Join a diverse, global team that combines strategic insight with hands-on execution to bring life-changing therapies to patients faster.
At Novotech, you’ll work alongside empowered teams driven by:
A strategic and proactive mindset
A culture of partnership, collaboration, and mutual respect
Ongoing support from senior leaders and global stakeholders
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