Remote Clinical Project Coordinator

Syneos Health, Inc.; Oklahoma; Hybrid; USD 41,000 - 80,000; Full time

Benefits offered by this job

Company car

Health benefits

401k match

Stock Purchase Plan

Bonus eligibility

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking a Project Specialist for Sponsor Dedicated/Remote work. You will provide project and operational support to the clinical team, assist with study coordination, documentation, and cross-functional collaboration in a dynamic environment.

The role requires entry-level clinical research exposure, familiarity with Veeva Vault and CTMS, strong Excel skills, and the ability to work independently while maintaining organizational rigor.

Qualifications

• Entry-level experience in Clinical Research and understanding of trial processes.
• Experience with Veeva Vault and CTMS.
• Self-motivated with ability to work independently.
• Strong problem-solving and organizational skills.
• Experience coordinating meetings and follow-up activities.
• Adaptable to 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

Problem-solving

Organizational skills

Meeting coordination

Adaptability

Excel skills

Tools

Veeva Vault

CTMS

Job description

Syneos Health, Inc. is seeking a Project Specialist for Sponsor Dedicated/Remote work. You will provide project and operational support to the clinical team, assist with study coordination, documentation, and cross-functional collaboration in a dynamic environment.

The role requires entry-level clinical research exposure, familiarity with Veeva Vault and CTMS, strong Excel skills, and the ability to work independently while maintaining organizational rigor.