Senior Clinical Data Associate (Sr. CDA)
Location: Remote, India
Job ID: R-01331314
Employment Type: Full-Time
Category: Clinical Research
Work Model: Fully Remote | Second Shift (Afternoons)
About the Role
Trialmed, the global site network and early-phase clinical solutions partner for PPD, part of Thermo Fisher Scientific, is seeking an experienced Senior Clinical Data Associate (Sr. CDA) to support and lead clinical data management activities across global research programs. This role offers the opportunity to work on high-impact clinical studies while ensuring exceptional data quality, compliance, and process excellence.
The Sr. CDA will function as a key contributor and supporting data manager for one or more projects, focusing on accurate data handling, collaboration across global teams, and adherence to Good Clinical Practice (GCP) standards.
Key Responsibilities
Support study setup activities including database design, data entry screen testing, and Data Validation Manual (DVM) creation.
Identify, resolve, and update data discrepancies within data management platforms.
Generate and track data clarifications and queries; support CRF design in relevant software when required.
Conduct comprehensive reviews of data listings for accuracy, consistency, and protocol alignment.
Serve as the subject-matter expert for study-specific data processes.
Provide training and work direction to junior data management staff.
Contribute to the enhancement of global data management processes and operational efficiencies.
Prepare and deliver project-specific status reports for management and client teams.
Perform Serious Adverse Event (SAE) and vendor data reconciliations, along with advanced data cleaning activities.
Apply strong analytical judgment to resolve complex data management challenges and recommend improvements.
Collaborate with external partners and internal stakeholders requiring strong communication and negotiation skills.
Ensure adherence to GCP, SOPs, WPDs, and regulatory requirements across all deliverables.
Required Education and Experience
Bachelor’s degree in life sciences, health sciences, or related field (or equivalent qualification).
Minimum 3+ years of experience in clinical data management or a related discipline.
Experience with EDC systems such as Medidata Rave and Veeva Vault is strongly preferred.
Knowledge of good documentation practices, eTMF, and clinical data workflows.
Equivalent combinations of education, training, and relevant experience may be considered.
Skills and Competencies
Strong understanding of clinical data management principles, GCP guidelines, and global SOP compliance.
High attention to detail with strong numerical, analytical, and problem-solving capabilities.
Excellent verbal and written communication skills with strong command of English.
Proficiency in Microsoft Office and ability to quickly learn new data systems and Generative AI tools.
Strong interpersonal, cultural awareness, and customer-focused approach when working with global teams.
Ability to work independently with moderate supervision while managing multiple deadlines.
Ability to maintain strict confidentiality of all clinical and proprietary data.
Strong organizational and time-management skills with flexibility to adapt to evolving project needs.
Working Conditions
Standard shift timing: 1:00 PM to 10:00 PM IST.
Work model options: Office-based, Hybrid, or Fully Remote depending on candidate preference.
All activities must comply with Good Manufacturing Practices (GMP) safety standards.
Why Join Us?
At Trialmed, part of the global PPD clinical research business of Thermo Fisher Scientific, you will contribute to clinical programs that advance global health. This role provides the opportunity to influence data quality in early-phase studies, collaborate with international teams, and support life-changing scientific innovation.
Apply today and become part of a team dedicated to making the world healthier, cleaner, and safer through excellence in clinical data management.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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Delhi | India | New Delhi | PAN-India |Assam :
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Nedlands |Queensland :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Netanya | Tel Aviv | Yavne | Kfar Saba | Be'Er Sheva |Remote :
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Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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