ICON plc Hiring for Clinical Trial Associate: Pharma Jobs
ICON plc is currently recruiting for the position of Clinical Trial Associate (CTA) in Bangalore. This opportunity is ideal for candidates from Life Sciences, Pharmacy, Nursing, or Healthcare backgrounds who are looking to begin or advance their careers in clinical research and clinical trial management.
As one of the world’s leading Contract Research Organizations (CROs), ICON partners with global pharmaceutical and biotechnology companies to support innovative drug development across multiple therapeutic areas. The CTA role offers hands‑on exposure to global clinical trials, regulatory documentation, essential study start‑up activities, and cross‑functional coordination within clinical operations.
For candidates aiming to build a strong foundation in clinical trial documentation, site support, and operational excellence, this Clinical Trial Associate job in Bangalore provides a credible platform to grow in the clinical research industry.
Job Overview
- Position: Clinical Trial Associate
- Department: Clinical research
- Location: Banglore
- Experience: 0.6 to 2 Years
- Qualification: B.Pharm, M.Pharm, BSc, MSc or equivalent
- Job Type: Full-Time
- Last date to apply: 01 March 2026
Key Responsibilities
- Trial Coordination & Compliance: Assist in the day‑to‑day coordination and administration of clinical trials, ensuring all activities adhere to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
- Document Management: Maintain, update, and organize essential clinical trial documentation, including study files, regulatory binders, essential documents, and submission packages.
- Study Material Preparation: Support the development and preparation of study‑related materials such as Informed Consent Forms (ICFs), Case Report Forms (CRFs), and other trial documents required during study start‑up and execution.
- Cross‑Functional Collaboration: Work closely with project managers, clinical research associates (CRAs), regulatory teams, and other cross‑functional groups to ensure effective communication and smooth operational execution.
- Tracking & Reporting: Contribute to the tracking and reporting of key clinical trial metrics, timelines, and milestones, helping the study team monitor overall trial progress and compliance.
Required Skills & Qualifications
- Educational Background: A Bachelor’s degree in a scientific, life sciences, pharmacy, or healthcare‑related field.
- Clinical Research Interest or Experience: Prior experience in clinical research is an advantage, but strong interest and willingness to learn clinical trial operations is equally valued.
- Knowledge of Clinical Trial Standards: Basic understanding of clinical trial processes, regulatory guidelines, and Good Clinical Practice (GCP) requirements.
- Organizational & Communication Skills: Excellent organizational abilities and strong written and verbal communication skills, essential for managing trial documentation and collaborating with study teams.
- Attention to Detail & Teamwork: Ability to work collaboratively in a fast‑paced environment while maintaining high attention to detail and consistently delivering quality work.
Preferred Skills & Experience (Good to Have)
Candidates with the following additional skills and experience will have an advantage:
- Regulatory & SOP Compliance: Applies clinical data management knowledge in a highly organized manner while strictly following regulatory guidelines, global SOPs, and specific client expectations.
- Strong Attention to Detail: Demonstrates exceptional accuracy, numerical aptitude, and the ability to work confidently with interactive computer systems and EDC platforms.
- Effective Communication: Possesses strong written and verbal English communication skills, with a solid command of grammar for clear documentation and professional interaction.
- Analytical & Problem‑Solving Ability: Shows strong organizational skills and the ability to identify, analyze, and resolve data‑related issues effectively.
- Independent & Guided Work Capability: Can work productively with moderate supervision while managing day‑to‑day tasks efficiently.
- Confidentiality & Data Integrity: Maintains a high level of confidentiality when handling clinical trial data and client‑proprietary information, ensuring data protection and compliance.
- Customer‑Focused & Collaborative: Exhibits excellent interpersonal skills, a strong customer service mindset, and the flexibility to work both independently and as part of a collaborative team.
- Sound Decision‑Making: Demonstrates good judgment and the ability to make informed decisions during routine and complex data management activities.
- Clinical Knowledge: Familiar with medical terminology, clinical trial processes, and essential CDM concepts.
- Protocol & DVM Understanding: Understands the study protocol and the Data Validation Manual (DVM), ensuring accurate and compliant data review and query handling.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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