Clinical Research Associate Jobs at IQVIA Biotech | Apply Now
A rare chance has emerged for aspiring professionals in clinical research associate jobs at IQVIA Biotech in New York, United States. This opportunity is ideal for candidates with experience in clinical trials, particularly in oncology,.
Job Details
- Position: Clinical Research Associate (CRA)
- Location: New York, United States of America
- Reference Number: R1520467
About IQVIA Biotech
IQVIA Biotech is a full-service Contract Research Organization (CRO) dedicated to serving biotech sponsors. With over 25 years of experience, the organization specializes in providing agile, therapeutically aligned solutions that facilitate the rapid delivery of breakthrough treatments to patients. The firm is headquartered in the United States and operates globally, making significant contributions to the life sciences sector, including life sciences associate jobs.
Clinical Research Associate Jobs Overview
IQVIA Biotech is seeking a dedicated Clinical Research Associate (CRA) to join their team. The successful candidate will play a key role in ensuring the successful execution of clinical trials. Responsibilities include monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. This role directly contributes to the integrity and quality of clinical research data.
Eligibility Criteria for Clinical Research Associate Jobs
- Bachelor’s degree in life sciences or health-related field (or equivalent experience).
- Requires at least 1 year of on-site monitoring experience.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Ability to travel as required by the project.
CRA Job 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.
Why Join IQVIA Biotech?
Joining IQVIA Biotech offers professionals a chance to work at the forefront of clinical research in life sciences jobs in New York. The organization prides itself on its commitment to integrity and professionalism, providing a supportive environment for career growth and development. Employees have the opportunity to contribute to meaningful projects that impact patient outcomes worldwide.
The clinical research associate vacancy at IQVIA Biotech presents an excellent opportunity for qualified candidates in New York to advance their careers in clinical research. With a focus on oncology and a commitment to quality, this role is crucial for the successful execution of clinical trials. Interested candidates should apply at the earliest to seize this opportunity in clinical research associate jobs.
