Abbott Hiring Clinical Research Associate
- Abbott Hiring Clinical Research Associate I | Gurgaon Opportunity for Life Sciences Professionals
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience:
- Required Skills
- Preferred Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Who can apply for this role?
- Is clinical research experience mandatory?
- What does a Clinical Research Associate do?
- What certifications are preferred?
- What is the job location?
Abbott Hiring Clinical Research Associate I | Gurgaon Opportunity for Life Sciences Professionals
Abbott is hiring for the role of Clinical Research Associate I (CRA I) in the Research & Development department at its Gurgaon location in India. This opportunity is ideal for candidates with a background in clinical research, life sciences, or healthcare who have at least 2 years of experience and are looking to grow in clinical trial operations and site management.
This role focuses on site management, regulatory document handling, and clinical trial support, making it a strong career opportunity for professionals aiming to build expertise in clinical monitoring, GCP compliance, and global clinical trials.
Company Overview
Abbott is a global healthcare leader known for developing innovative medical devices, diagnostics, nutrition products, and branded generic pharmaceuticals. With a strong presence in clinical research and medical technology, Abbott plays a critical role in advancing patient care and improving health outcomes worldwide.
The company operates across more than 160 countries and is recognized for its commitment to quality, regulatory compliance, and cutting-edge healthcare solutions. Working at Abbott provides exposure to global clinical trials, advanced technologies, and a strong learning environment in the pharmaceutical and medical device industry.
Job Role & Responsibilities
As a Clinical Research Associate I, you will support clinical trial site management activities, ensuring compliance with global regulatory standards and smooth execution of clinical studies.
Key Responsibilities:
Site Management & Regulatory Support
- Collect and review essential regulatory documents from clinical trial sites
- Ensure compliance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP)
- Maintain and update clinical trial documentation systems and study records
- Support creation and management of regulatory and patient binders
Clinical Trial Operations
- Assist in ensuring protocol compliance at assigned clinical sites
- Support follow-up and resolution of audit findings and monitoring visit issues
- Collaborate with site management teams and global clinical operations
- Maintain accurate trial data in systems like Study Organizer (SO)
Documentation & Data Management
- Manage electronic and paper-based regulatory documents
- Upload and maintain clinical trial data in internal systems
- Initiate translations for informed consent forms and study documents
Inventory & Logistics Management
- Coordinate clinical inventory management with site and warehouse teams
- Manage import/export processes as per regulatory requirements
- Liaise with project management teams and device accountability specialists
Eligibility / Qualifications
Educational Qualification:
Bachelor’s degree in Life Sciences, Nursing, Bioengineering, Pre-Medicine, or related fields
Relevant Courses:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc Nursing, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Biomedical Engineering, Clinical Research
Experience:
- Minimum 2 years of experience in clinical research or healthcare environment
- Familiarity with clinical trial processes and regulatory standards preferred
Required Skills
- Strong understanding of GCP and clinical research guidelines
- Excellent communication and interpersonal skills
- Analytical thinking and problem-solving abilities
- Proficiency in Microsoft Office tools
- Strong organizational and multitasking capabilities
Preferred Qualifications
- Certification from SoCRA or ACRP (Clinical Research Certification)
- Experience in clinical trial site management or hospital-based research
Location & Salary
- Job Location: Gurgaon, India
- Salary: Competitive salary package as per industry standards in clinical research and pharmaceutical sector
Application Process
Interested candidates can apply directly through the official Abbott careers portal:
Apply Here: https://www.jobs.abbott/us/en/job/ABLAUS31146021ENUSEXTERNAL/Clinical-Research-Associate-I
Frequently Asked Questions (FAQs)
Who can apply for this role?
Candidates with Life Sciences, Nursing, or Biomedical degrees and at least 2 years of experience can apply.
Is clinical research experience mandatory?
Yes, relevant experience in clinical research or healthcare settings is required.
What does a Clinical Research Associate do?
A CRA manages clinical trial sites, ensures regulatory compliance, and supports study execution.
What certifications are preferred?
Certifications like SoCRA or ACRP are beneficial but not mandatory.
What is the job location?
The role is based in Gurgaon, India.
| Category | Details |
|---|---|
| Company | Abbott |
| Vacancies | Clinical Research Associate I |
| Required Education | Life Sciences / Nursing / Biomedical Sciences |
| Experience | Minimum 2 Years |
To apply for this job please visit www.jobs.abbott.
