# Senior Clinical Trial Associate

**Company**: ICON Strategic Solutions
**Location**: Mumbai
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/Clinical-Trial-Assistant_JR155460?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e81f88cc-ce7

## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

**Job Role:** We are hiring a Clinical Trial Associate (CTA) in Mumbai, India to support global clinical trial operations for key oncology, cardiology, pulmonology, and immunology studies. The role is office-based in Mumbai, India with responsibility for critical documentation, system management, and cross-functional trial coordination.

**Responsibilities:**

- Support global study teams with trial documentation, TMF maintenance, and compliance.

- Manage and update Veeva Vault, CTMS, and EDC systems.

- Assist in study start-up, site document collection, and tracking.

- Coordinate meetings, minutes, training documentation, and trial communications.

- Track essential documents, milestones, and key study metrics.

- Liaise with internal teams, vendors, and site staff for timely deliverables.

- Maintain inspection-ready documentation and support audits.

**Your Profile:**

- Min. 3-5 years of experience working as a Clinical Trial Associate(CTA) in global clinical trials.

- Hands-on experience in core CTA activities including Ethics Committee (EC) submissions, Health Authority (HA) submissions, site payments, and essential clinical trial documentation and tracking.

- Strong understanding of clinical operations processes, ICH-GCP guidelines, and regulatory requirements.

- Proficiency in clinical systems such as Veeva Vault, CTMS, and EDC platforms.

- Excellent communication, documentation, and organisational skills with strong attention to detail.

- Ability to work effectively in a fast-paced, structured, and cross-functional global environment.

**Rewards & Benefits:** ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

- Competitive base salary and performance-related incentives

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programmes and wellbeing resources

- Learning and development opportunities through structured training and career pathways

## Skills

### Required
- Veeva Vault
- CTMS
- EDC
- ICH-GCP guidelines
- regulatory requirements

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/Clinical-Trial-Assistant_JR155460?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)