Remote Jobs at Syneos Health
Find your next remote opportunity · 121 Open Positions
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.
Site Activation Specialist
Site Activation Specialist supporting Canadian clinical-trial submissions, regulatory approvals, contracts, and end-to-end site activation for Syneos Health.
Medical Writer I / Medical Writer II, CSR Narratives
Medical writer creating clinical narratives, study reports, and regulatory documents for Syneos Health’s life sciences services. Reviewing clinical data and ensuring compliance with FDA, ICH-E3, and client standards.
Principal Statistician – Ophthalmology
Principal Statistician leading biostatistical analyses for ophthalmology clinical trials at Syneos Health. Mentoring statisticians, overseeing SAPs, programming specifications, quality control, and regulatory support.
Site Contracts Specialist II/Sr – Sponsor Dedicated
Site Contracts Specialist managing contracts, budgets, and negotiations for Syneos Health’s sponsored clinical trials. Coordinating site start-up, legal, finance, and clinical operations stakeholders.
Site Contracts Specialist II – Sponsor Dedicated
Site Contracts Specialist managing clinical trial agreements, budgets, and start-up documentation for Syneos Health. Supporting multi-country pharmaceutical and clinical research projects.
Senior Statistical Programmer, R, RShiny
Lead statistical programming for Syneos Health’s clinical drug development services using R/RShiny. Developing CDISC-compliant clinical trial outputs and mentoring programming teams.
Principal Medical Writer – Publications
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.
Global Site Identification and Feasibility Specialist – Sponsor-Dedicated
Global Site Identification and Feasibility Specialist supporting Syneos Health’s sponsor-dedicated clinical trials. Identifying high-performing sites and providing data-driven enrollment and study-planning insights.
Global Trials Optimization Specialist – Project Manager I
Global Trials Optimization Specialist supporting feasibility, recruitment, retention, and enrollment strategy for Syneos Health’s clinical research programs. Using data and cross-functional coordination to optimize global trial execution.
Principal Clinical Trial Regulatory Affairs
Principal Regulatory Affairs specialist leading complex clinical-trial submissions for Syneos Health, a global biopharmaceutical services organization. Managing regulatory strategy, dossiers, compliance, budgets, and client relationships across study lifecycles.
Project Manager – Clinical Trial Lead
Clinical Trial Lead managing global clinical studies for Syneos Health, a life sciences services organization. Leading project delivery, compliance, budgets, timelines, and client coordination.
Country Operations Associate
Country Operations Associate supporting clinical trial operations for Syneos Health, a life sciences services organization. Managing site activation, regulatory submissions, study documentation, contracting, tracking, and compliance.
Principal/Senior Medical Editor – Publications Documents
Principal/Senior Medical Editor quality-checking and leading medical writing deliverables for Syneos Health’s life-sciences services. Ensuring regulatory compliance, editorial accuracy, and on-time project delivery.
Site Contracts Specialist I – Contract Manager I, Sponsor Dedicated
Clinical contracts specialist managing trial agreements, amendments, CDAs, and site budgets for Syneos Health’s biopharmaceutical clients. Supporting study start-up and site activation across Argentina, Brazil, and Mexico.
Senior Statistical Programmer
Lead SAS statistical programmer developing and validating clinical-trial outputs for Syneos Health, a global life sciences services organization. Guiding programming teams and supporting drug development projects.
Senior CDA, Client Facing – Min 5+ Years Data Management Experience
Senior Clinical Data Associate leading data management, testing, reconciliation, and QC for Syneos Health’s global clinical trials. Home-based in Argentina, mentoring CDAs and supporting Project Data Managers.
Sponsor Dedicated Medical Writer II/Sr
Medical writer leading clinical, regulatory, and scientific documents for Syneos Health, a life sciences services organization. Collaborating with biopharmaceutical clients and cross-functional clinical teams.
Research Nurse – Per Diem
Per diem Registered Nurse conducting mobile clinical trials for pharmaceutical and healthcare companies. Coordinating patient visits, administering trial medication, collecting samples, and maintaining GCP-compliant data.
Research Nurse – Per Diem
Per-diem registered nurse conducting mobile clinical trials for biopharmaceutical and healthcare companies in Oahu. Managing patient visits, trial medication, samples, recruitment, and safety reporting.
Clinical Trial Manager – Project Management
Clinical Trial Manager overseeing sponsor-dedicated clinical monitoring and site management for Syneos Health, a global life sciences services organization. Ensuring compliance, data integrity, risk mitigation and study milestone delivery in Argentina.