Remote Clinical Project Specialist - Sponsor Support

Syneos Health/ inVentiv Health Commercial LLC

Arkansas

Remote

USD 41,000 - 80,000

Full time

2 days ago
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Benefits offered by this job

Company car/allowance
Health benefits
401k match
Stock Purchase Plan
Paid time off

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, and support study-related processes and documentation in a dynamic environment.

Entry-level professionals with knowledge of clinical trial processes, Excel, and tools like Veeva Vault and CTMS are encouraged to apply.

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
Excel
Independent Work
Organization

Tools

Veeva Vault
CTMS

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, and support study-related processes and documentation in a dynamic environment.

Entry-level professionals with knowledge of clinical trial processes, Excel, and tools like Veeva Vault and CTMS are encouraged to apply.

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