Remote Clinical Project Specialist

Syneos Health, Inc.

Oklahoma

Remote

USD 41,000 - 80,000

Full time

2 days ago
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Benefits offered by this job

Health benefits
Company car/allowance
401k match
Employee Stock Purchase Plan
Commissions/bonus
PTO & sick time

Job summary

Syneos Health in the United States is seeking a Project Specialist (Sponsor Dedicated/Remote) to provide project and operational support to the clinical team, assist with clinical project coordination and administrative activities, and support study-related processes. This role requires entry-level clinical research experience, proficiency with Veeva Vault and CTMS, and strong Excel skills.

You'll collaborate with cross-functional stakeholders in a dynamic environment and adapt to changing study

Qualifications

  • Entry-level experience in Clinical Research and understanding of trial processes.
  • Experience with Veeva Vault and CTMS.
  • Independent worker with strong time management and organizational skills.
  • Proficient in Microsoft Excel.
  • Able to coordinate meetings and follow-up activities.

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

Entry-level clinical research
Self-motivated
Strong problem-solving
Organizational skills
Meeting coordination
Adaptable
Excel skills

Tools

Veeva Vault
CTMS

Job description

Syneos Health in the United States is seeking a Project Specialist (Sponsor Dedicated/Remote) to provide project and operational support to the clinical team, assist with clinical project coordination and administrative activities, and support study-related processes. This role requires entry-level clinical research experience, proficiency with Veeva Vault and CTMS, and strong Excel skills.

You'll collaborate with cross-functional stakeholders in a dynamic environment and adapt to changing study

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