Overview
Join us as a Clinical Research Associate at the world’s largest and most comprehensive clinical research organization, empowered by healthcare intelligence.
Responsibilities
What You Will Be Doing :
- Manage all facets of site evaluation, initiation, monitoring, and close-out for multiple studies across various sites.
- Ensure that all trial conduct aligns with ICH GCP, FDA regulations, SOPs, and protocol requirements.
- Train site personnel on study protocols, systems, and operational procedures, ensuring clarity and compliance.
- Monitor and accurately document adverse event and serious adverse event reporting to prioritize patient safety.
- Work collaboratively with sites to devise and implement recruitment strategies that meet or exceed enrollment targets.
- Guarantee data integrity with comprehensive EDC oversight, prompt query resolution, and supportive database lock procedures.
- Maintain organized, audit-ready documentation in alignment with the Trial Master File.
- Oversee investigational product and non-clinical supply management effectively.
- Identify and resolve site performance, quality, or compliance issues with proactive intervention plans.
- Act as the primary liaison between site personnel and sponsor study teams, ensuring smooth communication and oversight.
Qualifications
You Are :
A holder of a Bachelor’s degree in Life Sciences or a Registered Nurse (RN).A Clinical Research Associate with at least 2 years of on-site monitoring experience in Oncology, specifically within solid tumor trials for a pharmaceutical company or CRO.Experienced with Graft-Versus-Host Disease (GVHD) studies.Located on the West Coast (PST) with the ability to travel regionally for 8-10 days each month.Possessing a valid driver's license and the capability for regular travel.Comfortable working within a dedicated Functional Service Provider model supporting one sponsor.Proficient in EDC, CTMS, IVRS, and Microsoft Office Suite.Knowledgeable of ICH GCP, HIPAA, FDA CFR, and other relevant guidelines.A strong communicator with excellent time management, attention to detail, and problem-solving capabilities.Able to work independently while also thriving in a collaborative matrix team environment.Pay Range ($91,336 / yr USD - $114,170 / yr USD)
Compensation will reflect factors such as geographic location, work experience, education / training, and skill set.What We Offer :
Our success is rooted in the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, we provide a robust array of benefits focused on well-being and work-life balance opportunities for you and your family :
Various annual leave benefits.A range of health insurance options tailored to meet you and your family’s needs.Competitive retirement planning options to maximize savings for your future.Access to a Global Employee Assistance Programme offering 24 / 7 support for you and your family.Life assurance.Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, and discounted gym memberships.At our organization, inclusion and belonging are integral to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. 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 you need reasonable accommodation during the application process or to perform essential job functions due to a medical condition or disability, please inform us.
Interested but unsure if you meet all of the qualifications? We encourage you to apply; you may be just what we’re looking for.