Project Associate

ICON plc · Healthcare & Pharma

India, Bangalore
Hybrid
Posted today
Operations & Supply Chain

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About the job

Project Associate (Bangalore - Hybrid Role)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Position: Project Associate

Location : Bangalore (Hybrid Role)

The Project Associate is responsible for preparing, reviewing, and finalizing bioanalytical study reports while ensuring compliance with study protocols, regulatory requirements, and internal quality standards.

The role requires collaboration with Project Management (PM), Quality Control (QC), Quality Assurance (QA), bioanalytical scientists, and study teams to address review comments, resolve discrepancies, and deliver accurate, compliant, and inspection-ready reports within defined timelines.

Key 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.

Good working knowledge of method development, method Validation, study sample analysis, ICH M10, and GLP/GCP requirements.

Hands-on experience with Watson LIMS, Electronic Laboratory Notebook (ELN) systems, and Microsoft Office applications (Word, Excel, etc.)

Experience working in a CRO or regulated bioanalytical laboratory environment is preferred.

Key Skills

Strong scientific writing and technical documentation skills for preparing clear and accurate reports.

Excellent attention to detail with a strong focus on data accuracy and report quality.

Good analytical and problem-solving skills to identify and resolve report-related discrepancies.

Effective communication and collaboration skills for working with cross-functional teams.

Ability to manage multiple projects efficiently and deliver reports within defined timelines.

Ability to independently address and resolve PM, QC, and QA review comments with minimal supervision.”

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

Are you a current ICON Employee? Please click here to apply

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