ICON is hiring for the position of Project Associate in Bangalore, Karnataka. This is a full-time hybrid opportunity for candidates with 1–3 years of experience in bioanalytical laboratories, clinical research, or regulated scientific documentation.
The selected candidate will be responsible for preparing, reviewing, and finalizing bioanalytical study reports while ensuring compliance with study protocols, regulatory requirements, and internal quality standards.
ICON Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | ICON |
| Job Position | Project Associate |
| Job Location | Bangalore, India |
| Work Mode | Hybrid (Office With Flex) |
| Job Type | Full Time |
| Experience | 1–3 Years |
| Qualification | Bachelor’s / Master’s Degree |
| Requisition ID | JR163464 |
| Job Category | Bioanalytical / Clinical Research |
| Application Mode | Online |
Position
Project Associate
The role focuses on bioanalytical study report preparation, scientific documentation, quality review, and coordination with cross-functional teams to ensure accurate and inspection-ready reports.
Key Responsibilities
- Prepare, review, and finalize bioanalytical study reports.
- Ensure compliance with study protocols, regulatory requirements, and internal quality standards.
- Collaborate with Project Management (PM), Quality Control (QC), Quality Assurance (QA), bioanalytical scientists, and study teams.
- Address review comments and resolve discrepancies in study reports.
- Maintain report accuracy, quality, and regulatory compliance.
- Deliver finalized reports within defined timelines.
- Independently address PM, QC, and QA review comments with minimal supervision.
Eligibility Criteria and Qualifications
Candidates interested in applying for the ICON Project Associate position should meet the following requirements:
- Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Biochemistry, Microbiology, or a related scientific discipline.
- 1–3 years of relevant experience in bioanalytical laboratories, clinical research, or regulated scientific documentation.
- Working knowledge of method development and method validation.
- Understanding of study sample analysis.
- Knowledge of ICH M10 and GLP/GCP requirements.
- Experience working in a CRO or regulated bioanalytical laboratory environment is preferred.
Required Skills
- Strong scientific writing and technical documentation skills.
- Good understanding of data accuracy and report quality.
- Excellent attention to detail.
- Analytical and problem-solving abilities.
- Ability to identify and resolve report-related discrepancies.
- Effective communication and cross-functional collaboration.
- Ability to manage multiple projects and meet deadlines.
- Hands-on experience with Watson LIMS and Electronic Laboratory Notebook (ELN) systems.
- Working knowledge of Microsoft Office applications, including Word and Excel.
