CRA Jobs at IQVIA, USA | Life Sciences | Apply Now
Explore exciting CRA jobs at IQVIA Biotech in San Francisco, a hub for clinical research associate opportunities. With a focus on life sciences jobs in the USA, IQVIA Biotech offers rewarding positions for professionals looking to advance their careers in clinical research.
- Job Title: CRA 2, Early Clinical Development
- Location: San Francisco, Carlsbad, Sacramento, United States of America
- Reference Number: R1554995
About The Company
IQVIA Biotech is a full-service Contract Research Organization (CRO) focused on serving biotech sponsors. With over 25 years of experience in the life sciences sector, IQVIA Biotech provides agile and therapeutically aligned solutions that help accelerate the development of breakthrough treatments for patients. Headquartered in the United States, the organization is dedicated to enhancing patient outcomes through innovative clinical research.
Job Description
The Clinical Research Associate (CRA) at IQVIA Biotech will play a crucial role in the execution of clinical trials. Responsibilities include monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. This position is essential for maintaining the integrity and quality of clinical research data in San Francisco.
CRA Jobs – Key Responsibilities
- Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
- Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
- Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
- Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
- Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
- Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
- Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
- Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
Eligibility Criteria Required For CRA Jobs
- Bachelor’s degree in life sciences or health-related field (or equivalent experience).
- Requires at least 1.5 years of on-site monitoring experience.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Ability to travel as required by the project.
Why Join IQVIA Biotech?
IQVIA Biotech is recognized as a leading global provider of clinical research services. The organization fosters an environment that promotes innovation and collaboration, making it an excellent place for professionals in the life sciences field. By joining IQVIA Biotech, employees contribute to meaningful advancements in healthcare, enhancing patient outcomes and population health worldwide.
In conclusion, CRA jobs at IQVIA Biotech in San Francisco offer a unique opportunity for professionals passionate about clinical research. As part of the life sciences jobs sector in the USA, these roles are pivotal in advancing healthcare innovations and improving patient outcomes.
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