Clinical Data Science Manager leading data scientists, client accounts, and global clinical - trial projects. Ensuring data quality, regulatory compliance, staffing, budgets, and operational delivery at Syneos Health.
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Syneos Health
Currently Hiring
About the company
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial 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 insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.
Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.
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33 jobs found
Medical Writer developing clinical protocols and regulatory documents for Syneos Health’s life sciences clients. Partnering with Clinical Scientists across oncology, hematology, and cell therapy studies.
Regulatory CMC Consultant guiding small - molecule submissions and Veeva RIM activities. Supporting Syneos Health’s integrated life - sciences and drug - development services.
Site Activation Specialist supporting clinical trial start - up, regulatory submissions, and site activation for Syneos Health. Coordinating country - level quality, compliance, feasibility, and investigator contract activities.
Regulatory CMC consultant guiding small - molecule submissions and global compliance strategies. Supporting life - sciences customers through regulatory agency interactions and cross - functional programs.
Clinical Trial Manager overseeing clinical monitoring, site management, risk mitigation and compliance. Supporting Syneos Health’s drug development and commercialization services for life sciences customers.
Medical Writer II developing clinical protocols and regulatory documents for Syneos Health, a life sciences services organization. Leading medical writing deliverables across clinical studies and regulatory submissions.
Biostatistician designing real - world evidence studies from EMR and claims data for Syneos Health. Applying causal inference, trial emulation, and statistical programming across healthcare projects.
Site Activation Specialist supporting clinical - trial site activation, regulatory submissions, contracts, and payments at Syneos Health. Remote role serving Canadian operations.
Senior medical writer leading regulatory documents for Syneos Health’s integrated life sciences services. Preparing submissions, clinical reports, and safety materials for Phase 2 and 3 studies.
Senior Medical Editor supporting regulated medical publications at Syneos Health, a life sciences services organization. Ensuring editorial quality, compliance, and on - time delivery of complex writing projects.
Regulatory Strategist guiding Latin American drug submissions and lifecycle management for Syneos Health’s life sciences services. Providing regional expertise, coordinating authorities, and leading cross - functional submission teams.
Regulatory Consultant using Veeva Vault RIM to coordinate drug regulatory submissions for Syneos Health. Supporting Vertex submission managers with publishing, project tracking, and content planning.
Clinical Data Reviewer supporting Syneos Health’s life sciences and drug - development services. Reviewing clinical data and collaborating on solutions that accelerate patient progress.
Clinical Data Reviewer evaluating oncology clinical trial data for Syneos Health, a life sciences services organization. Collaborating with Clinical Solutions teams to accelerate drug development and commercialization.
Clinical Data Reviewer evaluating oncology clinical trial data for Syneos Health, a life sciences services organization. Supporting drug development solutions for pharmaceutical and healthcare customers.
Site Activation Specialist supporting Canadian clinical - trial submissions, regulatory approvals, contracts, and end - to - end site activation for Syneos Health.
Spécialiste recrutant et accompagnant des volontaires pour les études cliniques de Syneos Health à Québec. Gestion des dossiers, rendez - vous et communications avec les participants.
Principal Medical Writer developing clinical and regulatory publications for Syneos Health’s life - sciences services. Leading complex documents, reviews, client coordination, and regulatory - compliant medical writing.
Clinical Trial Manager overseeing site, clinical and central monitoring for Syneos Health’s integrated life - sciences services. Managing risks, compliance, study systems and delivery milestones across clinical trials.