ICON Hiring Study Start-Up Specialist – Business Operations Associate Roles Clinical Research (Remote)
- ICON Hiring Study Start-Up Specialist – Business Operations Associate Roles in Clinical Research (Remote India)
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What is study start-up in clinical research?
- What career growth can I expect?
- Is this a remote job?
- Summary
ICON Hiring Study Start-Up Specialist – Business Operations Associate Roles in Clinical Research (Remote India)
ICON plc is hiring Business Operations Associate – Site and Study Start-Up Specialists across Bangalore, Chennai, and Trivandrum with a remote work model. This is a full-time clinical research role for professionals with experience in regulatory submissions, site activation, and study start-up operations.
Multiple openings are expected for experienced candidates looking to advance in clinical trial start-up, regulatory affairs, and CRO operations. This role is ideal for professionals aiming to work on global clinical trials and regulatory approvals.
Company Overview
ICON plc is a global leader in clinical research and healthcare intelligence, supporting pharmaceutical, biotechnology, and medical device companies across the entire drug development lifecycle.
With strong expertise in clinical trials, regulatory consulting, and data-driven healthcare solutions, ICON is known for delivering high-quality research outcomes and accelerating drug approvals worldwide.
Job Role & Responsibilities
As a Study Start-Up Specialist, you will manage site activation and regulatory processes to ensure smooth initiation of clinical trials.
Core Responsibilities
- Prepare and submit regulatory documents including clinical trial applications and ethics committee submissions
- Coordinate with regulatory authorities, investigators, and internal teams for approvals
- Manage study start-up timelines and ensure compliance with ICH-GCP and local regulations
- Maintain accurate documentation of submissions, approvals, and communications
- Provide guidance to study teams on regulatory requirements and best practices
- Support process improvements to enhance efficiency in study start-up activities
Eligibility / Qualifications
- Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research)
- Experience: Minimum 2 years in clinical research, regulatory affairs, or study start-up roles
- Strong understanding of ICH-GCP guidelines and regulatory requirements
- Experience in clinical trial submissions and site activation processes
- Excellent project management, communication, and coordination skills
Location & Salary
- Job Location: Bangalore, Chennai, Trivandrum (Remote / Hybrid flexibility)
- Work Mode: Remote
- Salary Range: ₹6 LPA – ₹12 LPA (approximate based on CRO and study start-up roles)
Application Process
Apply directly through the official ICON careers page:
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires at least 2 years of experience in clinical research or regulatory functions.
What is study start-up in clinical research?
Study start-up involves regulatory submissions, site activation, and approvals required before a clinical trial begins.
What career growth can I expect?
You can grow into Study Start-Up Manager, Clinical Project Manager, or Regulatory Affairs Specialist roles.
Is this a remote job?
Yes, this role offers remote or hybrid flexibility across multiple locations in India.
Summary
| Category | Details |
|---|---|
| Company | ICON plc |
| Vacancies | Business Operations Associate – Study Start-Up Specialist |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research) |
| Experience | Minimum 2 years in clinical research / regulatory / study start-up |
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