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.
Remote · Canada, United States
Design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. Collaborate cross-functionally to translate complex analytical results into actionable insights for decision-making.
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, Poland
The Clinical Data Reviewer performs specialized clinical data reviews ahead of significant project milestones to ensure data readiness and validity. They work as an extension of the clinical scientist to identify inconsistencies, highlight errors, and manage queries across large, multi-faceted data sets.
Remote · Canada, United States
Design and execute real-world evidence studies using EMR and claims data to inform clinical development, HEOR, and regulatory strategy. Collaborate cross-functionally to translate complex analytical results into actionable insights for decision-making.
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
Manage and track regulatory submission plans for products in development and on the market across US, EU, and global markets. Coordinate content plans within Veeva Vault RIM and support submission managers with project management activities.
Remote · Canada
The Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also coordinate submission activities and translate project timelines into actionable plans using Smartsheet and Microsoft Project.
Remote · Canada, Poland
Perform clinical review and interpretive analysis of oncology study data to ensure readiness for major project milestones. Identify data inconsistencies, generate queries, and collaborate with study teams to resolve discrepancies.
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 · Vernon, British Columbia, Canada
The Research Nurse will manage day-to-day trial activities, including protocol compliance, data documentation, and patient assessments. They are also responsible for administering trial medication, processing samples, and reporting adverse events to the project team.
Remote · Colombia
Lead pre-award strategy and commercial leadership for Real World Late Phase (RWLP) accounts, including RFP strategy and budget structures. Serve as the strategic account leader post-award to maintain portfolio performance and sustain senior-level sponsor relationships.
Remote · Canada
The role involves conducting longitudinal cohort studies and performing statistical analyses using SAS or R to create tables, listings, and graphs. Responsibilities include reviewing protocols and SAPs, assessing data quality, and utilizing real-world data from EHR and claims databases.
Remote · Canada
Leads the creation and review of complex medical writing deliverables, including clinical study reports and regulatory submissions, ensuring scientific accuracy and compliance. Manages document strategies and coordinates activities across departments while mentoring junior medical writers.
Remote · Canada, United States
The biostatistician will design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. They will apply robust statistical methodologies and collaborate cross-functionally to translate complex analytical results into actionable insights.
Hybrid · Toronto
The Senior Global Project Manager provides strategic leadership for Phase II and III clinical trials, ensuring global alignment and operational excellence across Immunology, Metabolic, and Oncology therapeutic areas. They are responsible for managing global trial preparation, conduct, and closeout while fostering cross-functional collaboration and ensuring regulatory compliance.
Remote · Canada
The Principal Medical Writer leads the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and maintain strong relationships with clients and internal departments.
Remote · Canada
The Senior/Principal Medical Editor manages complex medical writing projects while ensuring documents meet regulatory standards and internal quality requirements. They also provide technical expertise, mentor staff, and contribute to process improvement initiatives.
Remote · Canada
The Project Manager is responsible for managing the Trial Master File, coordinating study deliverables across internal departments and vendors, and overseeing financial performance. They also handle risk mitigation strategies, resource management, and client communication to ensure project success.
Remote · Serbia
The Regulatory Device CMC Manager supports strategies for marketed and development products by preparing and submitting regulatory CMC documentation for combination devices. The role provides guidance to cross-functional teams to ensure global regulatory requirements are integrated into development and commercial programs.
