Clinical Research Specialist

As a Clinical Research Associate, you will be joining a world-leading clinical research organization, driven by healthcare intelligence. You will be part of a dynamic team that is dedicated to delivering high-quality research solutions.

Our client is seeking an Oncology CRA in the Northeast Region who can manage all aspects of site evaluation, initiation, monitoring, and close-out for multiple studies across various sites. This role requires strong communication and problem-solving skills, as well as the ability to work independently and collaboratively within a matrix team environment.

• Manage all aspects of site evaluation, initiation, monitoring, and close-out for multiple studies across various sites.
• Ensure trial conduct adheres to ICH GCP, FDA regulations, SOPs, and protocol requirements.
• Train and retrain site personnel on study protocols, systems, and operational procedures.
• Monitor and document adverse event and serious adverse event reporting to ensure patient safety.
• Collaborate with sites to develop and execute recruitment strategies to meet enrollment targets.
• Ensure data integrity through EDC oversight, timely query resolution, and support of database lock.
• Maintain audit-ready documentation and reconcile with the Trial Master File.
• Monitor investigational product and non-clinical supply management.
• Identify and resolve site performance, quality, or compliance issues with effective intervention plans.

• Hold a Bachelor's degree in Life Sciences or be a Registered Nurse (RN).
• A Clinical Research Associate with a minimum of 2 years of on-site monitoring experience in Oncology, specifically solid tumor trials for a pharmaceutical company or CRO.
• Experienced with Graft-Versus-Host Disease (GVHD) studies.
• Based on the West Coast (PST), able to conduct regional travel up to 8–10 days per month.
• Must have a valid driver's license and the ability to travel regularly.
• Comfortable working in a dedicated FSP model supporting one sponsor.
• Proficient in EDC, CTMS, IVRS, and Microsoft Office Suite.
• Knowledgeable in ICH GCP, HIPAA, FDA CFR, and other applicable guidelines.
• A strong communicator with excellent time management, attention to detail, and problem-solving skills.
• Able to work independently and collaboratively within a matrix team environment.

• A competitive salary package.
• A range of health insurance offerings to suit your needs.
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

We are committed to providing an inclusive and accessible environment for all candidates. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, please let us know through our website.

Interested in the role? We encourage you to apply regardless – we would love to hear from you