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Walk-In Interview @ Bharat Parenterals – Hiring for Production, QC, QA, IT & More (0-10 Yrs Exp) – June 28, 30 & July 1, 2025

ICON plc is Hiring a Clinical Data Risk Analyst (Hybrid Role)

Job ID: JR130919 | Locations: Bangalore, Chennai, or Trivandrum, India
Job Type: Full-Time (Hybrid) | Posted: June 27, 2025

About ICON plc

global leader in clinical research since 1990, ICON operates in 53 countries, delivering innovative drug development solutions while ensuring compliance with FDA, EMA, and ICH standards. Recognized as a Great Place to Work (4.2/5 rating), we offer a collaborative environment with flexible work options.

Why Join ICON?

Impact global healthcare through cutting-edge clinical trials
Hybrid work model (Office + Flex) for work-life balance
Competitive salary + comprehensive benefits (health insurance, retirement plans)
Inclusive culture with career growth opportunities

Role: Clinical Data Risk Analyst

Key Responsibilities

  • Conduct risk assessments on clinical trial data to identify and mitigate issues

  • Develop risk management plans with cross-functional teams

  • Monitor data quality/integrity and report findings to stakeholders

  • Use statistical tools (SAS, R, Python) for risk analysis and visualization

  • Support regulatory submissions and audit documentation

Qualifications & Skills

✔ Education: Degree in Statistics, Life Sciences, or related field
✔ Experience: Proven track record in clinical data analysis/risk management
✔ Technical Skills:

  • Proficiency in statistical software (e.g., SAS, Spotfire)

  • Knowledge of risk assessment methodologies (e.g., RBM)
    ✔ Soft Skills:

  • Strong analytical thinking and problem-solving

  • Excellent communication for cross-team collaboration

Benefits at ICON

  • Health Insurance: Tailored plans for you and family

  • Retirement Security: Long-term planning support

  • Wellbeing: TELUS 24/7 Employee Assistance Programme

  • Life Assurance + Optional Perks: Childcare vouchers, gym discounts

How to Apply

  1. Apply Online: Visit ICON Careers Portal (Job ID: JR130919)

  2. Submit: Resume + required details

  3. Interview Process:

    • HR screening → Virtual/In-person interviews → Offer

Need accommodations? Email careers@iconplc.com.

Commitment to Diversity

ICON is an equal opportunity employer. We welcome applicants regardless of race, gender, religion, disability, or veteran status.

Why This Role Matters

You’ll ensure data integrity and compliance in clinical trials, directly impacting patient safety and drug approvals worldwide.

🔗 Apply Now: ICON Careers Portal

(Don’t meet all criteria? ICON encourages applicants with transferable skills!)

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