IQVIA
CRA 2 – IQVIA Biotech
IQVIA Biotech is a full‑service CRO built to serve biotech sponsors. With more than 25 years of experience, we deliver agile, therapeutically‑aligned solutions to accelerate breakthrough treatments to patients worldwide.
Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.
Key Responsibilities
Conduct all types of site visits—selection, initiation, monitoring, and close‑out—in alignment with the contracted scope, 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.
Depending on the project, support site‑level recruitment planning and financial management, including invoice collection and budget tracking.
Qualifications
Bachelor’s degree in life sciences or health‑related field (or equivalent experience).
At least one year of on‑site monitoring experience.
Strong understanding of GCP, ICH guidelines, and regulatory requirements.
Ability to travel as required by the project.
Salary and Benefits Potential base pay range (annualized): $87,200.00 – $145,300.00. The actual base pay may vary based on qualifications, location, and schedule. Incentive plans, bonuses, and other compensation may also be offered.
Equal Employment Opportunity IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
Location Houston, TX – Full‑time
Application Portable to apply and view details: https://jobs.iqvia.com
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Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.
Key Responsibilities
Conduct all types of site visits—selection, initiation, monitoring, and close‑out—in alignment with the contracted scope, 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.
Depending on the project, support site‑level recruitment planning and financial management, including invoice collection and budget tracking.
Qualifications
Bachelor’s degree in life sciences or health‑related field (or equivalent experience).
At least one year of on‑site monitoring experience.
Strong understanding of GCP, ICH guidelines, and regulatory requirements.
Ability to travel as required by the project.
Salary and Benefits Potential base pay range (annualized): $87,200.00 – $145,300.00. The actual base pay may vary based on qualifications, location, and schedule. Incentive plans, bonuses, and other compensation may also be offered.
Equal Employment Opportunity IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
Location Houston, TX – Full‑time
Application Portable to apply and view details: https://jobs.iqvia.com
#J-18808-Ljbffr