
Clinical Research Associate Sponsor Dedicated
Welcome to IQVIA! We are a leading global provider of clinical research and healthcare solutions, dedicated to improving patient outcomes. We are currently seeking a highly motivated and experienced Clinical Research Associate Sponsor Dedicated to join our team. As a vital member of our organization, you will play a critical role in the success of our trials by ensuring compliance with protocols, regulations, and timelines while maintaining the highest ethical standards. We are looking for individuals with a strong background in clinical research and a passion for making a difference in the lives of patients. If you are a driven and detail-oriented professional with exceptional communication and organizational skills, we encourage you to apply for this exciting opportunity.
- Conduct thorough and accurate review of study protocols to ensure compliance with regulations and timelines.
- Manage relationships with study sponsors and provide regular updates on trial progress and any potential issues.
- Develop and maintain strong knowledge of current regulations and guidelines related to clinical research.
- Participate in site initiation, monitoring, and close-out visits to ensure proper data collection and adherence to protocols.
- Collaborate with cross-functional teams to resolve any issues that may arise during the course of the trial.
- Ensure timely and accurate submission of study documents, including informed consent forms, regulatory documents, and study progress reports.
- Conduct site qualification visits to assess potential sites for study participation.
- Train and educate study site staff on study protocols, procedures, and regulations.
- Monitor site activities and data to identify potential risks and take appropriate action to mitigate them.
- Maintain accurate and complete documentation of all study-related activities and ensure data integrity.
- Communicate effectively and professionally with study sponsors, investigators, and study site staff.
- Adhere to all ethical standards and guidelines set forth by IQVIA and the industry.
- Assist with data management and analysis as needed.
- Continuously evaluate and improve processes to ensure efficiency and quality.
- Represent IQVIA in a professional and positive manner at all times.
Strong Understanding Of Good Clinical Practice (Gcp) Guidelines And Regulatory Requirements For Conducting Clinical Trials.
Bachelor's Degree In A Scientific Or Healthcare-Related Field, Such As Biology, Pharmacy, Or Nursing.
Minimum Of 3 Years Of Experience As A Clinical Research Associate (Cra) Or In A Similar Role In The Pharmaceutical Or Biotech Industry.
Excellent Project Management Skills, Including The Ability To Manage Multiple Studies Simultaneously And Meet Tight Deadlines.
Strong Communication And Interpersonal Skills, With The Ability To Effectively Collaborate With Cross-Functional Teams And Build Relationships With Study Sites And Investigators.
Data Management
Risk assessment
Project coordination
safety
Clinical trial management
Regulatory Knowledge
Study Monitoring
Subject Recruitment
Protocol Compliance
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 Sponsor Dedicated is $60,000-$120,000 per year. This can vary depending on factors such as location, experience, and company size. Some companies may also offer additional benefits 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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