Remote Jobs at Syneos Health
Find your next remote opportunity · 90 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.
CRA, Oncology – Part Time, Fixed Term Contract
Part Time Clinical Research Associate in Oncology with flexible work hours at Syneos Health, supporting clinical trials and ensuring compliance with regulations.
Lead CRA – Sponsor Dedicated, Fluent in German and English
Lead CRA responsible for managing relationships with clinical trial sites and overseeing oncology clinical trials. Ensure study compliance and training across site personnel and CRA teams while fostering successful stakeholder collaborations.
Principal Biostatistician, Sr Biostatistician – R/Rshiny
Principal Biostatistician role supporting drug development projects at Syneos Health. Involved in clinical data analysis, training, and statistical planning across EMEA.
Senior Project Specialist – Sponsor Dedicated
Senior Project Specialist at Syneos Health managing clinical project files and communications for study information. Collaborating with diverse teams to support clinical solutions for drug development.
Principal Clinical Trial Regulatory Affairs, +4 Years Experience in Regulatory Submissions in LATAM
Principal Clinical Trial Regulatory Affairs role requiring expertise in LATAM regulatory submissions. Responsibilities include strategic development activities and line management for staff members.
TMF Specialist – Safety Processing, Min 2 Years Experience in Central File Management
TMF Specialist managing safety processing for clinical trials at Syneos Health. Requires 2+ years in central file management and relevant pharmaceutical experience.
Proposal Writer
Proposal Writer creating high-quality proposal documents for Syneos Health's drug development and commercialization efforts. Collaborating with internal stakeholders to deliver customer-focused solutions.
Regulatory Device CMC Manager
Device CMC Manager supporting regulatory strategies for marketed and development products. Collaborating with cross-functional teams to ensure compliance with regulatory requirements at Syneos Health.
Director, Epidemiology RWE – Onco or Immunology
Director of Epidemiology RWE at Syneos Health focusing on Onco or Immunology. Leading study protocol development and managing epidemiological projects to enhance healthcare outcomes.
Senior Project Specialist – Sponsor Dedicated
Planning and coordinating clinical trial activities according to ICH-GCP for Syneos Health. Collaborating with trial team and managing all trial-related tasks in a timely manner.
Medical Writer I – Clinical Trial Transparency Specialist
Manage and facilitate anonymization of datasets and documents while collaborating with cross-functional teams at Syneos Health. Ensuring compliance with global clinical trial disclosure and transparency guidelines.
Senior Project Specialist – Real World Evidence
Senior Project Specialist supporting innovative pharmaceutical research programs focused on real-world data at Syneos Health. Role involves project coordination and operational support within RWE environments.
Site Contracts Specialist, Clinical Trials Experience
Site Contracts Specialist managing contract management processes for clinical trials at Syneos Health. Collaborating with internal/external teams and providing quality support for contract negotiations.
Site Contracts Specialist – Clinical Trials
Site Contracts Specialist managing clinical trial contracts for Syneos Health. Collaborating with global teams to streamline clinical trial processes across multiple countries.
Senior Payment Specialist – Sponsor-dedicated
Senior Payment Specialist managing payments for clinical trials at Syneos Health. Ensuring compliance with agreements and collaborating with internal teams for process improvements.
Safety & PV Specialist I
Safety & PV Specialist I process ICSR at Syneos Health, ensuring compliance with regulatory requirements and managing safety tracking systems.
Clinical Trial Manager II – Project Management, CRA
Clinical Trial Manager overseeing site management oversight and clinical monitoring deliverables in Chile for drug development. Collaborating with teams to ensure regulatory compliance and data integrity.
Senior Site Contracts Lead – China Mainland/Taiwan/Malaysia
Senior Site Contracts Lead role focusing on negotiating and managing clinical study agreements at Syneos Health. Collaborating with global teams to ensure compliance and effective contract execution.
Senior Data Acquisition Specialist – Non-CRF
Lead Clinical Data Associates managing data acquisition activities during global clinical trials. Oversee data management, quality checks, and support for project data manager.
Senior Medical Director – Psychiatry
Medical Director providing oversight in clinical studies for Syneos Health, partnering with innovators across drug development continuum. Leading clinical projects and mentoring teams in a crucial therapeutic area.