Clinical Research Associate Job in Gurgaon at Abbott apply online for CRA roles in clinical trials and site management opportunities.
Company Overview
Abbott is a globally recognized healthcare organization with expertise in medical devices, pharmaceuticals, diagnostics, and nutrition. The company is known for its innovation-driven approach and strong involvement in clinical research and patient care. Abbott provides excellent career opportunities for professionals in clinical operations and site management.
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 Requisition ID | 31146020 |
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 operations and regulatory documentation management. This position involves working closely with global teams (US & EMEA) to ensure compliance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP).
It is a strong opportunity for candidates with clinical research experience to advance in site management and clinical operations.
Key Roles & Responsibilities
Clinical Trial & Site Management
- Support collection and review of essential regulatory documents
- Ensure accuracy and completeness as per GCP and GDP guidelines
- Maintain clinical trial documentation systems and databases
- Assist in preparation of patient and regulatory binders
Regulatory & Compliance
- Ensure compliance with clinical protocols and regulatory standards
- Support resolution of audit findings and monitoring follow-ups
- Maintain and upload regulatory documents in study systems
Collaboration & Communication
- Work with global site operations teams (US and EMEA)
- Communicate with investigators, vendors, and internal stakeholders
- Support site-level issue resolution and escalation
Clinical Inventory & Logistics
- Manage clinical inventory and device accountability
- Coordinate with warehouse, project teams, and customer service
- Handle import/export processes as per regulatory requirements
Documentation & Process Support
- Initiate translation of study documents including informed consent forms
- Update internal clinical systems and trackers
- 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, GDP, and clinical trial processes
- Strong communication and interpersonal skills
- Organizational and analytical abilities
- Proficiency in Microsoft Office tools
- Ability to work independently and manage deadlines
- Attention to detail and 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
- Work on global clinical trials and medical device studies
- Exposure to regulatory and compliance processes
- Career growth in CRA and clinical operations roles
- Learning and development opportunities
Selection Process
The hiring process typically 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 provides strong exposure to clinical trial management, regulatory documentation, and global collaboration. It is ideal for professionals aiming to build a long-term career as a Clinical Research Associate. Working at Abbott enhances your experience in medical device trials and offers a pathway to advanced roles in clinical operations and project management.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Abbott or any recruiter. Candidates should verify details before applying.
Final Call-to-Action
Candidates with clinical research experience should apply immediately to take the next step in their CRA career with Abbott.
