CRA II

ICON; Bengaluru; Hybrid; INR 900,000 - 1,500,000; Full time

Job summary

ICON Strategic Solutions is recruiting a Clinical Research Associate II to join a sponsor-dedicated model, backed by a global CRO network. You will design and analyze clinical trials, interpret complex data, and contribute to advancing therapies that help patients worldwide.

You will conduct site visits, ensure protocol compliance, and collaborate with investigators while maintaining data integrity and patient safety across Phase II/III oncology trials.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• 4–5 years of experience as a Clinical Research Associate & On-Site Monitoring.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Has worked in Phase II & III Oncology Trials (Mandatory).
• Current or Prior experience in Therapeutic Areas like Immunology or Cardiology or Gastroenterology or Pulmonology.
• Strong organizational and communication skills, with attention to detail.
• Ability to travel at least 60% of the time (international and domestic) and should possess a valid driver’s license.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

CRA II

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.

Position: Clinical Research Associate II

Location: Mumbai (Hybrid Role)

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 4-5 years of experience as a Clinical Research Associate & On-Site Monitoring
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Has worked in Phase II & III Oncology Trials (Mandatory)
• CurrentorPriorexperienceinTherapeuticAreaslikeImmunologyor Cardiology orGastroenterologyorPulmonology
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What ICON can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here