Remote Clinical Trials Project Specialist

Syneos Health/ inVentiv Health Commercial LLC

Michigan

Remote

USD 41,000 - 80,000

Full time

2 days ago
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Benefits offered by this job

Health benefits
401k
Employee stock purchase plan
Paid time off
Sick time
Car allowance/Company car

Job summary

Syneos Health is seeking a Project Specialist (Sponsor Dedicated/Remote) to provide project and operational support to the clinical team and assist with coordination and study activities in a dynamic environment.

The role requires entry-level experience in Clinical Research, familiarity with Veeva Vault and CTMS, strong Excel skills, and the ability to work independently while collaborating with cross-functional teams.

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

Self-motivated
Microsoft Excel
Organizational skills
Independent worker
Meeting coordination

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 and assist with coordination and study activities in a dynamic environment.

The role requires entry-level experience in Clinical Research, familiarity with Veeva Vault and CTMS, strong Excel skills, and the ability to work independently while collaborating with cross-functional teams.

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