Clinical Research Associate I Job in Gurgaon at Abbott apply online for CRA roles in clinical trials and site management positions.
Company Overview
Abbott is a leading global healthcare organization with a strong presence in pharmaceuticals, medical devices, diagnostics, and nutrition. Abbott’s Medical Devices division plays a key role in advancing clinical research and patient care through innovative technologies. The company offers excellent career opportunities for professionals in clinical operations and research.
Job Overview (Job Details)
| Category | Details |
|---|---|
| Company Name | Abbott |
| Job Role | Clinical Research Associate I |
| Qualification | Bachelor’s in Life Sciences / Nursing / Bioengineering |
| Experience | Minimum 2 Years |
| Job Location | Gurgaon, India |
| Employment Type | Full-Time |
| Salary | Not Disclosed |
| Selection Process | Online Application + Interview |
| Application Mode | Online |
Job Location & Employment Type
- Location: Gurgaon (BPTP Park Centra), India
- Employment Type: Full-Time
- Department: Clinical Research / Site Operations
Role Overview
The Clinical Research Associate I (CRA I) role at Abbott focuses on supporting clinical trial site management and regulatory documentation. This position involves working closely with global clinical operations teams to ensure compliance with GCP and GDP standards.
It is an excellent opportunity for candidates with clinical research experience who want to grow in site management and clinical operations.
Key Roles & Responsibilities
Clinical Trial & Site Management
- Support site management activities including collection of regulatory documents
- Review and analyze documents for accuracy and compliance with GCP/GDP
- Maintain clinical trial documentation systems and databases
- Assist in creating patient and regulatory binders
Regulatory & Compliance Support
- Ensure compliance with clinical protocols and regulatory requirements
- Support audit findings resolution and monitoring follow-ups
- Maintain regulatory documentation and ensure timely uploads
Collaboration & Coordination
- Work with global teams including US and EMEA site operations
- Communicate with site staff, vendors, and internal stakeholders
- Liaise between site, warehouse, and project management teams
Clinical Inventory & Logistics
- Manage clinical inventory and device accountability
- Handle import/export processes as per regulatory guidelines
- Coordinate with local warehouse and customer service teams
Documentation & Process Support
- Initiate translations of study-related documents
- Update internal systems with clinical trial data
- Contribute to process improvements and best practices
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Nursing, Bioengineering, or related field
Experience
- Minimum 2 years of relevant experience in clinical research or site operations
Skills Required
- Knowledge of GCP and clinical trial processes
- Strong communication and interpersonal skills
- Analytical and organizational abilities
- Proficiency in Microsoft Office tools
- Ability to work independently and manage multiple tasks
- Attention to detail and documentation accuracy
Preferred Qualifications
- Certification from SoCRA or ACRP (or equivalent)
- Experience in clinical or hospital research settings
Salary & Benefits
- Salary: Not disclosed (as per company norms)
Benefits
- Opportunity to work in global clinical trials
- Exposure to medical device research and operations
- Career growth in CRA and clinical operations roles
- Learning and development opportunities
Selection Process
The hiring process generally includes:
- Online application submission
- HR screening
- Technical/clinical interview
- Final selection
How to Apply
Interested candidates should apply through the official Abbott careers portal.
Important Dates
- Application Status: Open (Apply as soon as possible)
Why Apply for This Pharma Job?
This role offers strong exposure to global clinical trial operations and site management. Candidates will gain hands-on experience in regulatory documentation, clinical compliance, and inventory management. It is a valuable opportunity for professionals aiming to advance their careers as Clinical Research Associates in a globally recognized organization.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Abbott or any recruiter. Candidates should verify all details before applying.
Final Call-to-Action
Candidates with clinical research experience should apply immediately to secure this opportunity and grow their career in CRA roles.
