Clinical Research Associate Job in Gurgaon at Abbott for experienced candidates with clinical trials, regulatory documentation, and site management experience roles available
Introduction
A promising opportunity is now available for candidates looking to build a career in clinical research and site management. Abbott is hiring for the position of Clinical Research Associate I in Gurgaon, offering exposure to global clinical operations and regulatory processes. This role is ideal for candidates with a science or healthcare background who want to work in a structured and compliance-driven environment. If you are detail-oriented and interested in clinical trials, this position can provide valuable industry experience.
Company Overview
Abbott Laboratories is a well-established multinational healthcare company known for its contributions in pharmaceuticals, medical devices, diagnostics, and nutrition. With a strong global presence, Abbott focuses on improving lives through innovative healthcare solutions. The company operates across multiple therapeutic areas and is recognized for maintaining high standards in research, compliance, and patient safety. Working with Abbott provides professionals the opportunity to engage in cutting-edge clinical research and collaborate with international teams.
Job Overview
| Job Title | Clinical Research Associate I |
|---|---|
| Company Name | Abbott |
| Location | Gurgaon, India |
| 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
This position is based in Gurgaon, Haryana, at BPTP Park Centra. It is a full-time, on-site role requiring regular collaboration with internal and global clinical teams. The role follows a standard work schedule and involves coordination with both domestic and international stakeholders.
Open Positions / Department Details
- Department: Clinical Research and Site Operations
- Division: Medical Devices
- Role Category: Entry to Mid-Level Clinical Research
- Reporting Structure: Works under supervision of Site Operations and Study Management teams
This position primarily supports clinical trial site management activities and regulatory documentation processes within the medical devices division.
Key Roles & Responsibilities
- Assist in collecting and organizing essential regulatory documents required for clinical trial sites
- Review and evaluate site documentation to ensure compliance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP) guidelines
- Maintain and update clinical trial data within internal document management systems
- Support preparation and maintenance of regulatory binders and patient documentation throughout the study lifecycle
- Coordinate with site teams and internal departments to ensure timely submission and tracking of regulatory documents
- Monitor site compliance activities under supervision and escalate any issues to appropriate management teams
- Collaborate with global clinical operations teams across regions including the US and EMEA
- Support audit readiness by ensuring documentation accuracy and completeness
- Assist in resolving findings from monitoring visits and regulatory audits
- Manage clinical inventory activities including coordination with warehouses and tracking of medical devices
- Act as a liaison between study sites, project teams, and logistics partners
- Handle documentation related to import and export of clinical trial materials as per local regulatory requirements
- Initiate and coordinate translation of study-related documents including informed consent forms
- Participate in process improvement initiatives and contribute to operational efficiency
- Maintain clear communication with stakeholders including vendors, contractors, and internal teams
Eligibility Criteria
Education:
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Bioengineering, or related fields
- Candidates with academic exposure to clinical research or healthcare disciplines will be preferred
Experience:
- Minimum of 2 years of relevant experience in clinical research, site management, or hospital-based clinical roles
- Candidates with prior exposure to clinical trials or regulatory documentation will have an advantage
Skills Required:
Technical Skills:
- Understanding of clinical trial processes and regulatory guidelines
- Familiarity with GCP and GDP standards
- Ability to review and manage clinical documentation
- Knowledge of clinical data systems and document management tools
- Proficiency in Microsoft Office applications
Soft Skills:
- Strong written and verbal communication skills
- Good analytical and problem-solving abilities
- Excellent organizational and time management skills
- Attention to detail and accuracy in documentation
- Ability to work independently and within a team environment
- Capability to coordinate multiple tasks efficiently
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a globally recognized healthcare organization
- Exposure to international clinical trial processes and systems
- Professional growth through continuous learning and development
- Collaborative work environment with global teams
Selection Process
The selection process for this role may include the following stages:
- Initial application screening
- Technical or functional interview (clinical research knowledge assessment)
- HR discussion focusing on communication skills and cultural fit
- Final selection and offer release
Candidates are advised to prepare thoroughly on clinical research fundamentals, regulatory guidelines, and documentation practices.
How to Apply
Interested and eligible candidates can apply through the official online application portal provided by the company. Ensure that your resume is updated with relevant clinical research experience and skills before applying.
Why Apply for This Pharma Job?
This opportunity at Abbott is ideal for candidates aiming to establish a strong foundation in clinical research and regulatory operations. The role offers hands-on experience in managing clinical trial documentation, interacting with global teams, and understanding compliance frameworks. Professionals working in this position gain exposure to real-world clinical trial environments, which can significantly enhance career prospects in CROs, pharmaceutical companies, and medical device organizations. Additionally, working with a reputed global brand adds credibility to your professional profile and opens doors to advanced roles in the future.
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
Candidates who meet the eligibility criteria and are interested in building a career in clinical research are encouraged to apply at the earliest. Early applications may increase the chances of selection, as hiring processes are often conducted on a rolling basis.
