Syneos Health is a leading biopharmaceutical solutions organization that accelerates customer success through integrated clinical, medical, and commercial insights to improve patient outcomes.
Morrisville, NC
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, commercial and real world insights into outcomes to address modern market realities. We bring together a talented team of professionals with a deep understanding of patient and physician behaviors and market dynamics. Together we share diverse insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health is powered by an authentic, inclusive and high-performance culture that cares for colleagues, customers, patients, communities and the environment.
On-site · Québec
The role involves processing, reviewing, and evaluating chromatographic data while ensuring the accuracy and consistency of electronic data transfers. The scientist will also communicate findings to study leads and provide technical support during regulatory inspections.
Remote · Canada
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety and regulatory compliance. Collaborates with functional leaders to coordinate study milestones and ensures the clinical project team adheres to contractual obligations and study protocols.
Remote · Canada
The Clinical Trial Manager is responsible for overseeing site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. They lead clinical teams, manage study tools like the Clinical Monitoring Plan, and collaborate with functional leaders to meet study milestones.
Remote · Canada
The Site Activation Specialist is responsible for managing site activation processes, including regulatory submissions and site selection support at the country level. They also handle contract and budget negotiations while ensuring compliance with project requirements and company SOPs.
Remote · Canada
The Site Activation Specialist manages the end-to-end site activation process, including regulatory and ethics committee submissions and investigator contract negotiations. They ensure all activities comply with project timelines, budgets, and quality standards while maintaining accurate documentation in the Trial Master File.
Remote · Canada
The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and maintaining the Investigator Site File.
Remote · Canada
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and oversee investigational product administration.
Remote · Canada
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.