CRA 2/Sr. CRA 1, Early Clinical Development, U.S., IQVIA Biotech
Are you passionate about driving the advancement of new medicines and therapies in the early stages of clinical development? Do you thrive in a fast-paced and dynamic environment? If so, IQVIA Biotech has an exciting opportunity for you as a CRA 2/Sr. CRA 1 in our Early Clinical Development team. In this role, you will play a vital role in supporting the development of cutting-edge treatments and therapies for patients in the U.S. As a member of our team, you will have the opportunity to collaborate with top industry professionals and gain valuable experience in the biotech field. To excel in this role, you will need to be detail-oriented, highly organized, and possess excellent communication and problem-solving skills. Join us in making a difference in the lives of patients and contribute to the future of healthcare.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in accordance with study protocols, ICH-GCP guidelines, and applicable regulations
Ensuring the accurate and timely collection, review, and submission of clinical trial data and documentation
Communicating effectively with study sites, study team members, and other stakeholders to ensure successful execution of clinical trials
Proactively identifying and addressing issues or risks that may impact study timelines, data quality, or patient safety
Maintaining and updating study documents, including study plans, study-specific training materials, and site visit reports
Participating in study team meetings and providing updates on site activities and overall study progress
Assisting with the development and implementation of study-specific training for investigative site staff
Contributing to the development and review of study-related documents, including protocols, informed consent forms, and case report forms
Collaborating with cross-functional teams, including data management and medical monitoring, to ensure high-quality and timely study deliverables
Staying current with industry trends, regulations, and best practices in clinical research and contributing to the continuous improvement of study processes and procedures
Upholding ethical and professional standards and adhering to company policies and procedures at all times
IQVIA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials in accordance with study protocols, ICH-GCP guidelines, and applicable regulations
Ensuring the accurate and timely collection, review, and submission of clinical trial data and documentation
Communicating effectively with study sites, study team members, and other stakeholders to ensure successful execution of clinical trials
Proactively identifying and addressing issues or risks that may impact study timelines, data quality, or patient safety
Maintaining and updating study documents, including study plans, study-specific training materials, and site visit reports
Participating in study team meetings and providing updates on site activities and overall study progress
Assisting with the development and implementation of study-specific training for investigative site staff
Contributing to the development and review of study-related documents, including protocols, informed consent forms, and case report forms
Collaborating with cross-functional teams, including data management and medical monitoring, to ensure high-quality and timely study deliverables
Staying current with industry trends, regulations, and best practices in clinical research and contributing to the continuous improvement of study processes and procedures
Upholding ethical and professional standards and adhering to company policies and procedures at all times
IQVIA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply tot his job
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