IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. We are seeking a Remote Clinical Research Associate (CRA) to join our dynamic team. In this role, you will play a pivotal part in ensuring the quality, safety, and integrity of clinical trials by monitoring clinical sites, supporting study execution, and maintaining regulatory compliance—all from the comfort of your remote workspace. This position is ideal for proactive professionals who thrive in a flexible, virtual environment while contributing to innovative clinical research that impacts patient lives worldwide.
Key Responsibilities
Conduct remote monitoring of clinical trial sites, ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Review and verify clinical trial data, ensuring accuracy, completeness, and compliance with regulatory standards.
Collaborate with cross-functional teams including project managers, data managers, and investigators to resolve study-related issues.
Maintain effective communication with clinical sites via phone, email, and virtual meetings to support site performance and compliance.
Prepare monitoring visit reports and document follow-up actions in a timely manner.
Participate in training and professional development activities to stay updated on industry standards and regulations.
Support audits and inspections by regulatory authorities, providing necessary documentation and data as required.
Required Skills and Qualifications
Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field (Master’s degree preferred).
Strong understanding of clinical trial processes, ICH-GCP guidelines, and FDA/EMA regulations.
Excellent attention to detail, analytical thinking, and problem-solving skills.
Proficient in electronic data capture (EDC) systems, Microsoft Office Suite, and remote collaboration tools.
Exceptional verbal and written communication skills for effective stakeholder interaction.
Self-motivated with the ability to work independently and manage multiple priorities in a remote environment.
Experience
Minimum of 1–3 years of experience as a Clinical Research Associate or in clinical monitoring roles.
Prior experience in remote or decentralized trial monitoring is highly desirable.
Experience with oncology, cardiology, or other therapeutic areas is a plus.
Working Hours
Flexible remote work schedule with availability for virtual meetings across time zones.
Full-time role; occasional weekend or after-hours coordination may be required depending on study demands.
Knowledge, Skills, and Abilities
Strong organizational and time-management skills to meet project deadlines.
Ability to interpret clinical protocols and assess site compliance.
Competence in risk-based monitoring approaches and data-driven decision making.
High level of integrity, professionalism, and commitment to patient safety.
Tech-savvy and comfortable navigating virtual monitoring platforms.
Benefits
Competitive salary with performance-based incentives.
Comprehensive health, dental, and vision insurance.
Flexible remote work environment promoting work-life balance.
Professional development programs, training, and career advancement opportunities.
401(k) retirement plan with company matching.
Employee wellness programs and mental health resources.
Why Join IQVIA
Joining IQVIA means becoming part of a global organization that is transforming healthcare through innovation and data-driven solutions. You will work alongside experts who are passionate about improving patient outcomes, contributing to cutting-edge clinical research, and shaping the future of healthcare. Remote work flexibility, continuous learning, and meaningful work make IQVIA an ideal place to grow your career while making a global impact.
How to Apply
Interested candidates should submit their resume/CV along with a cover letter highlighting relevant clinical research experience via the IQVIA careers portal: https://www.iqvia.com/careers Ensure your application clearly demonstrates your qualifications, remote work readiness, and commitment to clinical research excellence.