Clinical Trials Project Coordinator — Data & Documentation

Canfieldpublishing

Parsippany-Troy Hills (NJ)

On-site

USD 32,000 - 39,000

Full time

14 days+

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Benefits offered by this job

Benefits package including health/dent
401(k) plan with employer match
Discretionary bonus
Paid time off

Job summary

Canfield Scientific, Inc. is seeking a Clinical Project Associate to join our Clinical Services team in Parsippany, NJ. This role supports designated clinical project teams with project management, documentation, and data activities in a fast-paced environment.

The ideal candidate has an associate degree or 1 year of experience, strong Microsoft Office skills, and excellent time management, communication, and team collaboration abilities. Competitive hourly pay and comprehensive benefits offered.

Qualifications

  • Associate degree or at least 1 year work experience.
  • Proficiency in Microsoft Office.
  • Strong time management and organizational skills.
  • Ability to adjust to shifting priorities and meet deadlines.
  • Detail-oriented, flexible, and works well within a team environment.

Responsibilities

  • Provide project management and operational support to designated clinical project team ensuring that quality, timelines, and project specifications are met
  • Manage study documentation ensuring accuracy within the documentation while aiding in the preparation of supply shipments to study sites
  • Setup, maintain, and update databases and assist with data query resolution
  • Perform quality control checks to ensure the integrity of data and may support initiation phase of project
  • Communicate with study sites by fielding, answering, and directing questions to obtain information and direct to corresponding personnel

Skills

Time management
Communication skills
Multitasking
Problem-solving

Education

Associate degree

Tools

Microsoft Office

Job description

Canfield Scientific, Inc. is seeking a Clinical Project Associate to join our Clinical Services team in Parsippany, NJ. This role supports designated clinical project teams with project management, documentation, and data activities in a fast-paced environment.

The ideal candidate has an associate degree or 1 year of experience, strong Microsoft Office skills, and excellent time management, communication, and team collaboration abilities. Competitive hourly pay and comprehensive benefits offered.

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