Remote Sponsor-Dedicated Clinical Project Specialist

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

Job summary

Syneos Health is seeking a Project Specialist (Sponsor Dedicated/Remote) to provide project and operational support to the clinical team. You will assist with clinical project coordination and administrative activities, ensuring study-related processes and documentation stay on track.

The role requires entry-level experience in Clinical Research and familiarity with Veeva Vault and CTMS. You should be self-motivated, organized, and comfortable working in a dynamic, cross-functional environment,

Qualifications

• Entry-level experience in Clinical Research, with a solid understanding of clinical trial processes and study operations.
• Experience working with Veeva Vault and 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

Veeva Vault

CTMS

Independence / self-motivated

Problem-solving

Meeting coordination

Adaptability

Excel

Job description

Syneos Health is seeking a Project Specialist (Sponsor Dedicated/Remote) to provide project and operational support to the clinical team. You will assist with clinical project coordination and administrative activities, ensuring study-related processes and documentation stay on track.

The role requires entry-level experience in Clinical Research and familiarity with Veeva Vault and CTMS. You should be self-motivated, organized, and comfortable working in a dynamic, cross-functional environment,