Senior Clinical Data Associate | Thermo Fisher Scientific (Remote, India)
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Work Environment & Flexibility
- Application Process
- Why Join Thermo Fisher Scientific?
- FAQs
- Call to Action
- Summary Table
Senior Clinical Data Associate | Thermo Fisher Scientific (Remote, India)
Apply for Senior Clinical Data Associate role at Thermo Fisher Scientific, India. 3+ years of data management experience required. Fully remote.
Be part of a global organization that drives healthcare innovation and data excellence. Thermo Fisher Scientific, through its Trialmed (PPD Clinical Research) division, is hiring for a Senior Clinical Data Associate (Sr CDA) position in India. This full-time remote opportunity offers the chance to collaborate with international teams in managing complex clinical data for global clinical trials.
This role is designed for skilled clinical data professionals who possess strong technical acumen, deep understanding of Good Clinical Practice (GCP), and the ability to lead data validation and management projects that contribute to the development of life-saving therapies.
Company Overview
Thermo Fisher Scientific Inc. is a world leader in science and innovation, operating with the mission: to make the world healthier, cleaner, and safer. Its Clinical Research business (PPD) delivers clinical trial solutions to major biopharma and biotech organizations worldwide, advancing the development of new treatments and improving patient outcomes.
Through Trialmed, Thermo Fisher’s early phase clinical research solution, professionals get the opportunity to contribute to cutting-edge clinical studies that push the boundaries of medical science.
Job Role & Responsibilities
The Senior Clinical Data Associate (Sr CDA) is responsible for overseeing the quality, accuracy, and integrity of clinical trial data. This includes database design, data cleaning, validation, and reporting in accordance with international regulatory and company standards.
Key Responsibilities:
- Support study setup activities, including database design, edit check programming, and Data Validation Manual (DVM) creation.
- Identify, resolve, and document data discrepancies and queries.
- Conduct in-depth data listing reviews for accuracy and consistency.
- Lead CRF design and data validation processes for assigned studies.
- Ensure compliance with Good Clinical Practice (GCP), SOPs, and project timelines.
- Perform SAE reconciliation, vendor data integration, and data listing review.
- Serve as a subject matter expert (SME) for specific study-level processes.
- Provide mentorship and training to junior data associates.
- Contribute to process improvement initiatives across the global data management team.
- Create periodic status reports for management and sponsors.
Leadership & Collaboration:
- Coordinate effectively with global cross-functional teams.
- Serve as data management point of contact for sponsors and internal stakeholders.
- Ensure that project deliverables meet quality, budget, and timeline requirements.
Eligibility / Qualifications
Educational Background:
- Bachelor’s degree (or equivalent) in Life Sciences, Pharmacy, Information Technology, or related field.
Experience Requirements:
- Minimum 3+ years of experience in Clinical Data Management (CDM) or related clinical research domains.
- Hands-on experience with Electronic Data Capture (EDC) systems such as Medidata Rave, Veeva Vault, or equivalent.
Core Competencies:
- Excellent attention to detail and strong analytical mindset.
- Good understanding of clinical trial protocols, CRFs, DVMs, and data flow processes.
- Familiarity with GCP, ICH, and global clinical data standards.
- Excellent communication skills in English (both written and verbal).
- Strong organizational and multitasking abilities with focus on meeting project deadlines.
- Proficiency in MS Office applications (Excel, Word, Outlook, PowerPoint).
Preferred:
- Knowledge of Good Documentation Practices (GDP), eTMF systems, and AI-based data automation tools.
- Prior experience with global CROs or biopharma organizations.
Location & Salary
- Work Type: Fully Remote (India)
- Work Schedule: Second Shift (Afternoons) – 1:00 PM to 10:00 PM IST
- Department: Clinical Research / Data Management
- Employment Type: Full-Time, Regular
- Compensation: Competitive salary with global exposure and flexible work options.
Work Environment & Flexibility
- Flexible hybrid or remote work setup.
- Adherence to all Good Manufacturing Practices (GMP) and Safety Standards.
- Opportunity to collaborate across global teams in the US, EU, and APAC regions.
Application Process
Interested candidates can apply directly through Thermo Fisher’s global careers portal. Ensure your resume reflects relevant clinical data experience and system proficiency.
👉 Apply Here – Thermo Fisher Careers Portal
Apply before positions close! Join a company where your expertise drives scientific breakthroughs that save lives.
Why Join Thermo Fisher Scientific?
- Work with a global leader in contract research and clinical data management.
- Gain exposure to diverse therapeutic areas and innovative technologies.
- Be part of a team that supports the world’s top biopharma organizations.
- Career growth through structured training and mentorship programs.
- Inclusive, diverse, and performance-driven work culture.
- Explore exciting Clinical Data Management Jobs in India, Remote Pharma Jobs, and Global CRO Careers with Thermo Fisher Scientific.
FAQs
Q1: Who can apply for the Senior Clinical Data Associate role at Thermo Fisher Scientific?
Candidates with a bachelor’s degree in Life Sciences, Pharmacy, or IT and a minimum of 3 years of experience in Clinical Data Management are eligible.
Q2: Is the position remote?
Yes. The role is fully remote for candidates based in India.
Q3: What are the shift timings?
The standard working hours are 1:00 PM to 10:00 PM IST (Second Shift).
Q4: What EDC tools are used?
Primarily Medidata Rave, Veeva Vault, and other global data systems.
Q5: What makes Thermo Fisher a great employer?
Thermo Fisher offers global exposure, world-class projects, career development, and a mission-driven culture.
Q6: What is the application deadline?
Applications are open until positions are filled — early applications are encouraged.
Call to Action
🚀 Take your clinical data management career to the next level with Thermo Fisher Scientific! Be part of a global organization advancing medical research and innovation.
👉 Click Here to Apply – Senior Clinical Data Associate, Remote India
Apply now and help make the world healthier, cleaner, and safer.
Summary Table
| Category | Details |
|---|---|
| Company | Thermo Fisher Scientific (Trialmed / PPD Clinical Research) |
| Vacancy | Senior Clinical Data Associate |
| Required Education | Life Sciences, Pharmacy, Information Technology |
| Experience | Minimum 3+ Years |
| Location | Remote, India |
| Work Schedule | 1:00 PM – 10:00 PM IST (Second Shift) |
| Department | Clinical Research / Data Management |
| Job Type | Full-Time, Regular |
| Apply Link | Apply Here |
To apply for this job please visit jobs.thermofisher.com.
