Clinical Data Manager / Programmer

Syreon is an international health research corporation with headquarters in North America, Europe and other global locations, working with world experts in academia, industry and healthcare sectors across the fields of precision medicine and real-world research. Our research programs engage patients, providers, producers, payers and policy makers through large-scale research networks using adaptive decentralized research studies to evaluate innovative therapies designed to transform the care of these devastating and costly diseases.

Syreon's Clinical Data Management division is looking for an experienced Data Manager to join our multi-disciplinary unit in the ongoing support of cutting-edge research programs. This full-time role is an opportunity to collaborate with a dynamic team of researchers in maintaining the highest standards in the conduct of research activities. The primary activity of the Clinical Data Manager is to assist in the provision of data management services including but not limited to, leading studies independently from initial study set up, data processing and study close out activities. The Clinical Data Manager will be required to create data review guidelines/specifications and manage studies effectively with excellent project planning skills. This position is highly interactive and involves the application of advanced database functionality and standard operating procedures.

Syreon is a leading Clinical Research Organization conducting international clinical trials and health economics and outcomes research across a broad range of chronic and rare diseases.

In this role, you will:
• Design and validate clinical databases, including designing or testing logic checks
• Perform quality control audits to ensure accuracy, completeness, or proper usage of clinical systems and data
• Process clinical data, including receipt, entry, verification, or filing of information
• Generate data queries, based on validation checks or errors and omissions identified during data entry, to resolve identified problems
• Develop project-specific data management plans that address areas such as coding, reporting, or transfer of data, database locks, CRFs and work flow processes
• Monitor work productivity or quality to ensure compliance with standard operation procedures
• Prepare appropriate formatting to data sets as requested
• Design forms for receiving, processing, or tracking data
• Prepare data analysis listings and activity, performance, or progress reports
• Analyze clinical data using appropriate statistical tools
• Write work instruction manuals, data capture guidelines, or standard operation procedures
• Contribute to the compilation, organization, and production of protocols, clinical study reports, regulatory submissions, or other controlled documentation
• Track the flow of work forms, including in-house data flow or electronic forms transfer

To be successful in this role, you likely:
• Have a bachelor's degree in life sciences, including at least 3 years industry experience within the health sciences/CRO or pharmaceutical industry
• Are passionate about clinical research/clinical trials
• Have good knowledge in medical terminology and Electronic Data Capture (EDC) process
• Have excellent knowledge of ICH/GCP, FDA, and HPB regulations
• Programming skills or experience with SAS or R is an asset
• Possess strong attention to details and thorough in achieving quality work to meet company standards
• Have strong interpersonal and leadership skills, including adaptability, flexibility, and professional integrity