Central Monitor II

📋 Description

• • Syneos Health is a leading integrated biopharmaceutical solutions organization dedicated to accelerating customer success by translating unique clinical, medical affairs, and commercial insights into tangible outcomes that address the complexities of modern market realities.
• • Our Clinical Development model places the customer and patient at the core of every initiative, driving continuous improvement and streamlining operations to enhance both external and internal collaboration.
• • Join a global team of over 29,000 passionate problem solvers across 110 countries, united by a shared mission to innovate and accelerate the delivery of life-changing therapies.
• • As a Central Monitor II, you will play a pivotal role in ensuring the integrity and quality of clinical trial data through advanced analytical techniques and proactive risk management.
• • You will be instrumental in supporting the Central Monitoring Lead by managing the study-specific setup and ongoing maintenance of the data analytical tool essential for centralized monitoring activities.
• • This role demands expertise in Risk-Based Quality Management (RBQM) data analytical tools, enabling you to conduct thorough data risk reviews and effectively manage identified risks and issues.
• • A key responsibility involves contributing to the training and education of central and local study teams, imparting knowledge on RBQM principles and central monitoring processes to foster a culture of quality and compliance.
• • You will actively perform centralized monitoring of study data, meticulously maintaining oversight of study, country, and site risk parameters in strict accordance with the study monitoring plan.
• • Your analytical skills will be crucial in identifying data quality trends that may indicate systematic errors or potential performance issues at the study, country, or site level.
• • You will be responsible for clearly communicating identified trends, their implications, and recommended actions to relevant study team members, utilizing the data analytical tool and providing regular, comprehensive status reports.
• • Ensuring the proper documentation and archiving of all instream data reviews, risk assessments, and issue management activities is a critical aspect of this role, maintaining a robust audit trail.
• • You will share the responsibility for upholding data quality standards at the study, country, and site levels, contributing directly to the overall success and reliability of clinical trials.
• • This position offers the opportunity to work remotely, providing flexibility while contributing to groundbreaking pharmaceutical solutions.
• • Syneos Health is committed to fostering a culture of development, offering career progression, supportive management, comprehensive training, and recognition programs.
• • Embrace our 'Total Self' culture, where authenticity and diversity are celebrated, creating an inclusive environment where everyone feels they belong.
• • Contribute to a company that has partnered with 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products over the past five years, impacting thousands of studies, sites, and patients globally.
• • Take initiative and challenge the status quo in a dynamic, competitive, and ever-evolving industry.
• • Learn and grow within an organization that values innovation, collaboration, and a commitment to improving patient lives worldwide.
• • This role is integral to our mission of accelerating the delivery of therapies and making a significant impact on global health.