ICON is inviting applications for the position of Clinical Trial Associate (Clinical Trial Administrator) at its Bangalore, India office. This opportunity is ideal for B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Nursing, Biotechnology, and other healthcare graduates who are interested in building a career in Clinical Research, Clinical Trial Management, and Clinical Operations.

As a global Clinical Research Organization (CRO), ICON offers professionals the opportunity to work on international clinical studies while gaining exposure to regulatory documentation, study coordination, and trial administration.

If you’re searching for Clinical Trial Associate Jobs in Bangalore, Clinical Research Jobs for Life Sciences Graduates, or ICON Careers India, this opportunity deserves your attention.

Job Overview

Key Responsibilities

As a Clinical Trial Associate at ICON, you will:

• Coordinate and support clinical trial activities.
• Maintain Trial Master Files (TMF) and essential study documentation.
• Organize regulatory documents and study records.
• Assist in preparing informed consent forms (ICFs).
• Support Case Report Form (CRF) documentation activities.
• Ensure compliance with ICH-GCP guidelines and study protocols.
• Coordinate with Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs), investigators, and cross-functional teams.
• Track clinical study milestones and project timelines.
• Support regulatory submission documentation.
• Maintain accurate clinical trial records throughout the study lifecycle.

Eligibility Criteria

Applicants should possess:

• Bachelor’s degree in a scientific or healthcare-related discipline.
• Educational backgrounds such as:
  • B.Pharm
  • Pharm.D
  • M.Pharm
  • B.Sc
  • M.Sc
  • Biotechnology
  • Microbiology
  • Biochemistry
  • Life Sciences
  • Nursing
  • Allied Health Sciences
• Strong interest in Clinical Research.
• Understanding of Clinical Trial processes.
• Basic knowledge of:
  • ICH-GCP
  • Clinical Research
  • Regulatory Guidelines
  • Clinical Documentation
• Excellent communication and organizational skills.
• Ability to work in collaborative project teams.

Preferred Skills

Candidates with knowledge of the following will have an advantage:

• Clinical Trial Management
• Trial Master File (TMF)
• Clinical Trial Documentation
• Case Report Forms (CRFs)
• Informed Consent Process
• Regulatory Compliance
• Clinical Operations
• Good Documentation Practices (GDP)
• Microsoft Office
• Attention to Detail

Salary (Expected)

Based on similar Clinical Trial Associate positions in India, the expected salary is approximately:

₹4.8 LPA – ₹8.5 LPA

Actual compensation depends on qualifications, skills, and relevant experience.

Employee Benefits

ICON offers an attractive employee benefits package including:

• Competitive salary
• Annual performance incentives
• Health insurance
• Medical, dental, and vision benefits (where applicable)
• Retirement and pension plans
• Life insurance
• Disability coverage
• Employee Assistance Program (EAP)
• Learning and Development programs
• Global career growth opportunities
• Flexible working environment

Why Join ICON?

ICON is one of the world’s leading Clinical Research Organizations (CROs), supporting pharmaceutical, biotechnology, and medical device companies in bringing innovative medicines to patients faster.

Employees benefit from:

• Global clinical research exposure
• International projects
• Career development programs
• Inclusive work culture
• Strong learning environment
• Opportunities for long-term career growth

How to Apply

Application Link