Remote Clinical Project Coordinator

Syneos Health, Inc.; Missouri; Remote; USD 41,000 - 80,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits (Medical, Dental, and/

Company 401k match

Stock Purchase Plan eligibility

Commissions/Bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health is seeking a Project Specialist to provide project and operational support to the clinical team in a remote-capable role. You will assist with coordination and administrative activities, helping to manage study-related processes and documentation.

Ideal candidates have entry-level clinical research exposure, familiarity with CTMS and Veeva Vault, and strong Excel, organizational, and problem-solving skills in a dynamic environment.

Qualifications

• Entry-level experience in Clinical Research, with a solid understanding of clinical trial processes and study operations.
• Experience working with: Veeva Vault; CTMS (Clinical Trial Management Systems)
• Self-motivated with the ability to work independently and take ownership of tasks.
• Strong problem-solving and organizational skills.
• Experience coordinating meetings and managing follow-up activities.
• Adaptable and comfortable working in a dynamic environment.
• Strong Microsoft Excel skills.

Responsibilities

• Provide project and operational support to the clinical team.
• Assist with clinical project coordination and administrative activities.
• Support study-related processes and documentation.
• Work in a dynamic environment where priorities and processes may vary from study to study.
• Collaborate with cross-functional stakeholders.
• Demonstrate flexibility and adaptability as departmental needs evolve.
• Help identify and resolve operational issues proactively.

Skills

Clinical research basics

Independent work

Organizational skills

Meeting coordination

Adaptability

Microsoft Excel

Tools

Veeva Vault

CTMS

Job description

Syneos Health is seeking a Project Specialist to provide project and operational support to the clinical team in a remote-capable role. You will assist with coordination and administrative activities, helping to manage study-related processes and documentation.

Ideal candidates have entry-level clinical research exposure, familiarity with CTMS and Veeva Vault, and strong Excel, organizational, and problem-solving skills in a dynamic environment.