
Clinical Research Associate, Sponsor Dedicated
Welcome to IQVIA, the world's leading provider of clinical research services. We are seeking a highly motivated and experienced individual to join our team as a Clinical Research Associate, Sponsor Dedicated. In this role, you will have the opportunity to work closely with our sponsors to ensure the success of clinical trials. As a key member of our team, you will play a critical role in advancing medical research and improving patient outcomes. We are looking for someone with a strong background in clinical research and a passion for making a difference in the healthcare industry. If you have a keen attention to detail, excellent communication skills, and a drive for excellence, we invite you to apply for this exciting and rewarding position.
- Conduct clinical trial activities in accordance with company policies, SOPs, FDA regulations, and ICH/GCP guidelines.
- Serve as the primary point of contact for sponsors, providing regular updates and addressing any concerns or issues.
- Monitor the progress of clinical trials, ensuring they are conducted according to protocol and within timelines.
- Verify accuracy and completeness of all clinical trial documentation, including study protocols, informed consent forms, and case report forms.
- Collaborate with cross-functional teams to ensure timely resolution of any study-related issues.
- Conduct site initiation, interim, and close-out visits, ensuring compliance with all regulatory requirements.
- Assist with the development and review of study protocols, informed consent forms, and other study-related documents.
- Perform source data verification and ensure timely and accurate data entry into electronic data capture systems.
- Maintain study files and records in an organized and compliant manner.
- Participate in study team meetings and provide regular updates on study progress.
- Identify and escalate any potential risks or issues that may impact study timelines or data integrity.
- Stay current with industry trends and regulations related to clinical research.
- Train and mentor new team members as needed.
- Foster positive relationships with sponsors, investigators, and study site staff.
- Continuously strive for excellence and contribute to the overall success of clinical trials and the company's mission.
Proficiency In Data Management And Experience With Electronic Data Capture (Edc) Systems.
Bachelor's Degree In A Relevant Scientific Field Such As Biology, Chemistry, Or Pharmaceuticals.
Minimum Of 2 Years Of Clinical Research Experience, Preferably In A Monitoring Role.
Strong Knowledge Of Good Clinical Practice (Gcp) Guidelines And Fda Regulations.
Excellent Communication And Interpersonal Skills, With The Ability To Collaborate Effectively With Cross-Functional Teams.
Quality Assurance
Data Management
Risk assessment
Regulatory Submission
Site Monitoring
Adverse Event Reporting
Protocol Compliance
Study Start-Up
Gcp Knowledge
Site Training
Investigator Engagement
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Associate, Sponsor Dedicated in Chicago, IL, USA is $70,000-$100,000 per year. This range may vary depending on factors such as experience level, qualifications, and the specific company or organization the individual is working for. Salaries may also be affected by the cost of living in a particular area. It is important to note that salaries can also vary significantly within this range based on individual performance and bonuses.
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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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