Apply for Clinical Research Associate I at Abbott 2026. Check eligibility, salary, experience, responsibilities, and application process details online now today.
Clinical Research Associate I at Abbott 2026 – Salary, Eligibility & Apply Online
Introduction
Clinical research is a rapidly expanding field in India, offering excellent career opportunities for life science graduates. The Clinical Research Associate I at Abbott is a great opportunity for candidates with clinical trial experience who want to work on global studies and site management activities. This role provides hands-on exposure to regulatory documentation, compliance, and clinical operations.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Research Associate I |
| Company Name | Abbott |
| Location | Gurgaon, India |
| Employment Type | Full-Time |
| Department | Research & Development / Clinical Operations |
| Experience Required | 2+ Years |
| Education | Bachelor’s Degree in Life Sciences / Nursing / Bioengineering |
| Salary | As per company norms |
Company Overview
Abbott is a globally recognized healthcare leader focused on developing innovative medical devices, diagnostics, nutrition products, and branded generic medicines. With a strong presence in India and worldwide, Abbott plays a key role in advancing clinical research and improving patient outcomes.
Job Location & Employment Type
The role is based in Gurgaon, India, and is a full-time position. It involves collaboration with global teams across the US and EMEA regions.
Open Positions / Department Details
This position is part of the Clinical Site Operations team, where the selected candidate will support site management activities, regulatory documentation, and clinical trial coordination.
Key Roles & Responsibilities
- Support site management activities and regulatory document collection
- Review and analyze regulatory documents for accuracy and completeness
- Ensure compliance with GCP (Good Clinical Practice) and GDP standards
- Maintain clinical trial documentation in internal systems
- Assist in creation and maintenance of patient and regulatory binders
- Support compliance with clinical protocols across study sites
- Collaborate with site teams to resolve audit findings and issues
- Manage clinical inventory and coordinate with warehouses and stakeholders
- Handle import/export processes as per regulatory guidelines
- Facilitate translation of study documents including informed consent forms
- Contribute to process improvements and operational efficiency
- Communicate effectively with cross-functional teams and stakeholders
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Nursing, Bioengineering, or related field
Experience
- Minimum 2 years of experience in clinical research or related field
- Experience in clinical trials or hospital settings preferred
Skills Required
- Strong understanding of clinical trial processes and regulations
- Knowledge of GCP and GDP guidelines
- Good analytical and documentation skills
- Proficiency in MS Office tools
- Strong communication and interpersonal skills
- Ability to manage multiple tasks and deadlines
- Attention to detail and organizational skills
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global healthcare leader
- Exposure to international clinical trials
- Career growth in clinical research and site management
- Learning and development opportunities
- Collaborative and professional work environment
Selection Process
The hiring process typically includes:
- Resume screening
- HR interview
- Technical/clinical interview
- Final selection
How to Apply
Interested candidates can apply through the official Abbott careers portal. Ensure your resume highlights your clinical research experience, regulatory knowledge, and site management skills.
Important Dates
- Last Date to Apply: Not specified (Apply early)
Why Apply for This Job?
The Clinical Research Associate I at Abbott offers a strong platform for professionals to grow in clinical research and site management. This role provides global exposure, hands-on experience with regulatory processes, and opportunities to work with international teams. It is ideal for candidates aiming to advance in clinical operations and research.
FAQs
1. What experience is required for this role?
Candidates need at least 2 years of experience in clinical research or related fields.
2. What qualifications are required?
A Bachelor’s degree in Life Sciences, Nursing, or Bioengineering is required.
3. Is certification required?
Not mandatory, but certifications like SoCRA or ACRP are preferred.
4. What are the main responsibilities?
Handling regulatory documents, site management support, and clinical trial coordination.
5. What is the job location?
The role is based in Gurgaon, India.
Conclusion
The Clinical Research Associate I role at Abbott is an excellent opportunity for professionals looking to build a career in clinical research. With global exposure, structured learning, and career advancement opportunities, this position is ideal for those aiming to grow in clinical operations and regulatory compliance. Apply early to maximize your chances.
Disclaimer
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