• A seasoned Global Oncology Clinical Data Manager with over 10 years of experience in managing data for Phase I-III clinical trials. Expert in database migration, EDC setup, data cleaning, vendor and regulatory documents and ensuring compliance with ALCOA principles.

• Led multiple projects involving database design, case report form (CRF) creation, data review, and reconciliation using tools like Medidata Rave, Veeva Vault, and SAS programming.

• Proven track record in vendor management, including working with vendor for clinical for database migrations and patient stratification. Adept at creating detailed project timelines, test scripts, and managing cross-functional teams to ensure data accuracy and regulatory compliance.

At Serious Data, we are supported by a team of trusted industry advisors who enhance the capabilities of our data management experts. These advisors bring extensive experience and deep expertise in clinical trial monitoring, biostatistics, and advanced data analytics. Their strategic guidance, from developing innovative data management frameworks to applying machine learning and predictive analytics, empowers our team to maintain the highest standards of data integrity and compliance. With their support, we ensure that our clients receive tailored, high-quality solutions, fostering efficiency, reducing risks, and delivering actionable insights that drive success in complex clinical trials.

Plans are in place to onboard 8 Clinical Data Managers with extensive experience in data management, data entry, data cleaning, and reporting. They will be strategically located in key markets to meet the needs of major clinical research hospitals.