Clinical Research Associate II - Oncology/Hematology

4w4 weeks ago

ICON plc

Blue Bell, US · Full-time · $91,336 – $114,170

About this role

As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data to contribute to the advancement of innovative treatments and therapies. This is a sponsor-dedicated position seeking a CRA with oncology/hematology experience.

Your day-to-day involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety while performing data review and resolving queries to maintain high-quality clinical data.

You will collaborate closely with investigators and site staff to facilitate smooth study conduct, working within a values-driven organization that prioritizes integrity, collaboration, agility, and inclusion. This role requires approximately 60% travel and the ability to work independently in a fast-paced environment.

ICON offers a competitive total rewards package designed to support your health, wellbeing, and career development, including structured training and career pathways. As a global healthcare intelligence and clinical research organization, ICON is united by a mission to bring new medicines and treatments to patients faster.

Requirements

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 1 year of experience as a Clinical Research Associate.
Monitoring experience with hem/onc studies.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational skills with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (approximately 60%).
Must be located in PA, NY, NJ, MA, ME, VT, NH, CT, or RI.

Responsibilities

Design and analyze clinical trials, interpreting complex medical data to advance innovative treatments and therapies.
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborate with investigators and site staff to facilitate smooth study conduct.
Perform data review and resolution of queries to maintain high-quality clinical data.
Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Take responsibility for your deliverables and work collaboratively within a sponsor-dedicated team.

Benefits

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.