Clinical Research Associate, Sponsor Dedicated

Welcome to IQVIA, a leading global provider of clinical research services and solutions. We are currently seeking a dedicated and driven Clinical Research Associate to join our team as a Sponsor Dedicated CRA. In this role, you will be responsible for supporting our sponsor clients in the successful execution of clinical trials. As a vital member of our team, you will play a crucial role in ensuring the safety and efficacy of novel treatments and therapies. If you have a passion for clinical research and a strong understanding of FDA regulations and ICH-GCP guidelines, we encourage you to apply. Join us in our mission to improve healthcare and make a positive impact on patients' lives.

1. Support Sponsor Clients: The primary responsibility of the Sponsor Dedicated CRA will be to provide support to our sponsor clients and ensure their satisfaction with our services. This includes building and maintaining strong relationships, addressing any issues or concerns, and providing frequent updates on trial progress.
2. Clinical Trial Execution: The CRA will be responsible for the successful execution of clinical trials on behalf of our sponsor clients. This will involve coordinating with various stakeholders, including investigators, study coordinators, and site staff, to ensure all trial activities are conducted in compliance with protocol, FDA regulations, and ICH-GCP guidelines.
3. Safety and Efficacy: As a vital member of our team, the CRA will play an essential role in ensuring the safety and efficacy of novel treatments and therapies. They will be responsible for monitoring and reporting adverse events, managing data collection and review, and ensuring all trial activities are conducted in compliance with safety regulations.
4. Compliance: The CRA will be responsible for maintaining compliance with all relevant regulations, including FDA regulations and ICH-GCP guidelines. This includes ensuring all trial activities are conducted in accordance with the approved protocol, and all necessary documentation is completed accurately and in a timely manner.
5. Data Management: The CRA will be responsible for managing and reviewing trial data to ensure accuracy and completeness. This includes verifying the accuracy of data entered, identifying and resolving any discrepancies, and ensuring data is collected in compliance with the protocol and regulatory requirements.
6. Communication and Collaboration: The CRA will be expected to communicate and collaborate effectively with internal and external stakeholders, including study teams, sponsor clients, and site staff. This will include providing regular updates, addressing any issues, and facilitating communication between all parties involved in the trial.
7. Training and Development: As a member of our team, the CRA will be responsible for staying up-to-date on industry trends, FDA regulations, and ICH-GCP guidelines. They will also be responsible for participating in training and development activities to enhance their skills and

According to JobzMall, the average salary range for a Clinical Research Associate, Sponsor Dedicated is $65,000-$95,000, with a median salary of $80,000. However, salaries can vary depending on factors such as location, experience, and employer. Some Clinical Research Associates may also receive bonuses and benefits in addition to their base salary.

IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.