Apply for Informed Consent Specialist job at ICON plc India. Check eligibility, salary, responsibilities, and application process details today.
Introduction
If you are planning to build a strong career in clinical research and regulatory documentation, this opportunity can be a valuable step forward. The Informed Consent Specialist Job at ICON plc offers professionals a chance to work on global clinical trials while ensuring ethical and regulatory compliance. This role is especially suitable for candidates with experience in ICF development and site start-up activities.
Job Overview
| Field | Details |
|---|---|
| Job Title | Informed Consent Specialist |
| Company Name | ICON plc |
| Location | Bangalore / Chennai / Trivandrum |
| Employment Type | Full-Time (Office with Flex) |
| Department | Clinical Research / Site Activation |
| Experience Required | 4 – 8 Years |
| Education | Life Sciences / Pharmacy / Related Field |
| Salary | As per company standards |
Company Overview
ICON plc is a leading global clinical research organization (CRO) that provides healthcare intelligence and clinical development services. The company collaborates with pharmaceutical, biotechnology, and medical device organizations to accelerate drug development and improve patient outcomes.
ICON is known for maintaining high standards in clinical trials, ensuring compliance with international regulations, and promoting innovation in healthcare research.
Job Location & Employment Type
- Locations: Bangalore, Chennai, Trivandrum (India)
- Work Mode: Office with flexible working options
- Employment Type: Full-time
Open Positions / Department Details
- Department: Clinical Trial Start-Up / Site Activation
- Role Focus: Informed Consent Form (ICF) development and compliance
- Interaction with global teams, sponsors, and regulatory authorities
Key Roles & Responsibilities
- Develop, review, and approve Informed Consent Forms (ICFs) and Subject Information Sheets (SIS)
- Create global templates and adapt them for country-specific and site-specific requirements
- Ensure compliance with ICH-GCP guidelines and applicable regulatory requirements
- Collaborate with sponsors, clinical teams, and project managers
- Manage and respond to queries from Ethics Committees, IRBs, and regulatory bodies
- Track timelines and ensure timely approval of ICF documents
- Maintain accurate documentation for Trial Master File (TMF)
- Act as a subject matter expert and provide training when required
- Support audits, inspections, and internal reviews
- Mentor and guide new team members
Eligibility Criteria
Education
- Degree in Life Sciences, Pharmacy, Biotechnology, or related discipline
Experience
- 4 to 8 years of experience in clinical research
- Experience in feasibility, site start-up, or site activation
- Minimum 2 years of hands-on experience in ICF writing or development
Skills Required
- Strong knowledge of ICH-GCP guidelines
- Excellent written and verbal communication skills in English
- Understanding of regulatory requirements for clinical trials
- Strong analytical and problem-solving abilities
- Attention to detail and accuracy in documentation
- Ability to work in a collaborative environment
Salary & Benefits
Salary: As per company standards
Additional benefits include:
- Annual leave and work-life balance initiatives
- Health insurance for employees and dependents
- Retirement and financial planning support
- Employee Assistance Program for well-being
- Life insurance coverage
- Flexible benefits such as gym memberships and travel support
Selection Process
The selection process may include the following stages:
- Application screening
- HR interview
- Technical or functional interview
- Final discussion with hiring manager
- Offer and onboarding
How to Apply
Candidates who meet the eligibility criteria can apply through the official online careers portal of the company.
Important Dates
- Application deadline not specified
Why Apply for This Job?
The Informed Consent Specialist Job at ICON plc provides an excellent platform for professionals looking to advance in clinical research and regulatory documentation. This role offers exposure to international clinical trials, opportunities to work with global teams, and the chance to build expertise in regulatory compliance.
It is a suitable opportunity for candidates aiming to grow in the CRO industry, develop specialized skills in ICF writing, and contribute to ethically conducted clinical research.
FAQs
Who can apply for this job?
Candidates with a background in life sciences, pharmacy, or biotechnology and relevant clinical research experience can apply.
What is the salary for this role?
The salary is offered as per company standards along with additional benefits.
Is experience required for this role?
Yes, candidates must have 4 to 8 years of experience, including at least 2 years in ICF writing.
How can I apply for this job?
You can apply through the official careers portal of ICON plc.
What skills are important for this position?
Strong regulatory knowledge, communication skills, attention to detail, and teamwork are essential.
Conclusion
The Informed Consent Specialist Job at ICON plc is a strong opportunity for experienced professionals in clinical research. With global exposure, structured career growth, and a supportive work environment, this role can help you advance your career in regulatory and clinical operations.
Disclaimer
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