Welcome to IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are currently seeking a highly motivated and detail-oriented individual to join our team as a Clinical Research Associate I. In this role, you will play a critical role in facilitating and managing clinical trials, ensuring the safety and efficacy of new treatments and therapies. If you have a passion for making a difference in the healthcare industry and possess strong organizational and communication skills, we encourage you to apply for this exciting opportunity.
- Facilitate and manage clinical trials: Responsible for coordinating and overseeing the various aspects of clinical trials, including study start-up, patient recruitment, data collection, and study close-out.
- Ensure safety and efficacy of treatments: Monitor and track patient safety and data integrity throughout the duration of clinical trials, following all applicable regulatory guidelines and best practices.
- Maintain accurate records: Keep detailed and organized records of all study activities, including patient data, study documents, and correspondence with study sites and sponsors.
- Communicate effectively: Serve as a liaison between study sites, sponsors, and internal team members, providing timely and accurate updates on study progress and any issues or concerns that arise.
- Conduct site visits: Perform on-site monitoring visits to study sites, ensuring protocol compliance, data accuracy, and adherence to all regulatory requirements.
- Train and educate study personnel: Provide training and support to study site staff on proper study procedures, data collection, and regulatory compliance.
- Identify and resolve issues: Proactively identify and address any issues or challenges that may arise during the course of the study, working with team members to find solutions and ensure study timelines are met.
- Collaborate with cross-functional teams: Work closely with project managers, data managers, and other team members to ensure seamless coordination and execution of clinical trials.
- Stay current with industry trends: Keep up-to-date with industry developments, regulations, and best practices, and apply this knowledge to the execution of clinical trials.
- Demonstrate a commitment to quality: Follow all company policies and procedures, as well as applicable regulatory guidelines, to ensure high-quality and compliant clinical trials.
Strong Communication And Organizational Skills
Bachelor's Degree In A Relevant Field (E.g. Life Sciences, Pharmacy, Nursing)
Prior Experience In Clinical Research, Preferably As A Clinical Research Coordinator Or Assistant
Knowledge Of Ich-Gcp Guidelines And Fda Regulations
Ability To Travel Up To 50% For Site Visits And Meetings
Project Management
Data Analysis
Quality Control
Regulatory compliance
Site management
Patient Recruitment
Protocol Review
Adverse Event Reporting
Investigator Training
Good Clinical Practice (GCP)
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Associate I is $50,000-$70,000 per year. This can vary depending on factors such as location, company size, and years of experience. Senior Clinical Research Associates can earn an average salary of $80,000-$100,000 per year. Again, this can vary depending on individual factors.
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IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.

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