Abbott Hiring for Clinical Research Associate Job in Gurgaon for experienced candidates with clinical trials, regulatory documentation, and compliance experience opportunities available
Introduction
Candidates looking to grow in the field of clinical research and regulatory operations have a valuable opportunity with Abbott in Gurgaon. The company is hiring for the role of Clinical Research Associate I, offering hands-on exposure to global clinical trial processes and site management activities. This position is suitable for professionals with a background in life sciences or healthcare who want to strengthen their expertise in clinical documentation and compliance. It provides a structured environment to learn, collaborate, and contribute to international clinical projects.
Company Overview
Abbott Laboratories is a globally recognized healthcare organization known for innovation in pharmaceuticals, medical devices, diagnostics, and nutrition products. The company operates across multiple countries and focuses on delivering advanced healthcare solutions that improve patient outcomes. Abbott maintains strong compliance standards in clinical research and offers professionals an opportunity to work in a highly regulated and growth-oriented environment.
Job Overview
| Job Title | Clinical Research Associate I |
|---|---|
| Company Name | Abbott |
| Location | Gurgaon, Haryana |
| Employment Type | Full-Time |
| Qualification | Bachelor’s Degree (Life Sciences / Healthcare preferred) |
| Experience | Minimum 2 Years |
| Salary | As per company norms |
| Application Mode | Online |
Job Location & Employment Type
The role is based at BPTP Park Centra, Gurgaon, Haryana. This is a full-time, on-site position requiring coordination with internal teams and global clinical operations across regions such as the US and EMEA. The role follows a standard work schedule and involves regular interaction with clinical sites and stakeholders.
Open Positions / Department Details
- Department: Clinical Site Operations
- Division: Medical Devices
- Role Level: Entry to Mid-Level
- Work Area: Clinical Research and Regulatory Documentation
This role focuses on supporting clinical trial execution through documentation, compliance, and coordination activities.
Key Roles & Responsibilities
- Assist in collecting and managing essential regulatory documents required for clinical trial sites
- Carefully review documentation to ensure accuracy, completeness, and compliance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP) standards
- Maintain and update clinical trial records in internal systems and databases
- Ensure timely uploading and tracking of regulatory documents in study management platforms
- Support the preparation and maintenance of investigator site files and patient documentation throughout the study lifecycle
- Work closely with site teams and internal stakeholders to ensure smooth execution of clinical projects
- Assist in monitoring site compliance and escalate issues when necessary
- Contribute to resolving findings from monitoring visits, inspections, or audits
- Coordinate with cross-functional teams including site management, operations, and project teams
- Handle clinical inventory tracking and coordination with local warehouses and logistics teams
- Support import and export processes related to clinical trial materials in accordance with regulatory requirements
- Facilitate translation of study-related documents including patient consent forms when required
- Participate in improving internal processes and maintaining operational efficiency
- Ensure effective communication with vendors, customers, and internal teams
Eligibility Criteria
Education:
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Bioengineering, or related healthcare disciplines
- Academic exposure to clinical research or medical sciences is preferred
Experience:
- Minimum 2 years of relevant experience in clinical research, site coordination, or hospital-based clinical roles
- Candidates with prior experience in regulatory documentation or clinical trial support will be preferred
Skills Required:
Technical Skills:
- Basic understanding of clinical trials and regulatory frameworks
- Knowledge of GCP and GDP guidelines
- Experience in handling clinical documentation and compliance processes
- Familiarity with document management systems and clinical databases
- Proficiency in Microsoft Office tools
Soft Skills:
- Strong communication and interpersonal abilities
- Analytical thinking and attention to detail
- Effective time management and organizational skills
- Ability to multitask and meet deadlines
- Capability to work independently and within a team
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a leading global healthcare company
- Exposure to international clinical research standards
- Learning and development opportunities in clinical operations
- Collaborative and professional work environment
Selection Process
The hiring process typically involves:
- Initial screening of applications
- Technical or functional interview focusing on clinical research knowledge
- HR interview to assess communication and cultural fit
- Final selection and offer
Candidates should be prepared with knowledge of clinical trial processes, documentation standards, and regulatory compliance.
How to Apply
Interested candidates should apply through the official online application system provided by the company. Ensure that your resume highlights relevant experience in clinical research, documentation, and compliance.
Why Apply for This Pharma Job?
This role provides an excellent platform for professionals aiming to build a strong career in clinical research. Working with Abbott allows candidates to gain practical exposure to clinical trial management, regulatory documentation, and global collaboration. The position helps develop critical skills such as compliance handling, data management, and cross-functional coordination. It is particularly beneficial for those seeking long-term growth in pharmaceutical, CRO, or medical device industries. The experience gained in this role can open doors to advanced positions in clinical operations and regulatory affairs.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
If you meet the eligibility criteria and are interested in advancing your career in clinical research, do not miss this opportunity. Apply as soon as possible to increase your chances of being considered for this role.
