Clinical Projects Associate — Data & Documentation

Canfieldsci

Parsippany-Troy Hills (NJ)

On-site

USD 32,000 - 39,000

Full time

14 days+

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Job summary

Canfield Scientific, Inc. is seeking a Clinical Project Associate to provide project management and operational support for designated clinical projects. The role involves ensuring quality, timelines, and project specifications are met, while aiding in documentation and supply shipments to study sites.

The ideal candidate has an associate degree or at least 1 year of experience, strong Microsoft Office skills, and excellent time management and teamwork abilities in a fast-paced environment.

Qualifications

  • Associate degree or at least 1 year work experience.
  • Proficiency in Microsoft Office.
  • Strong time management, problem-solving, and organizational skills.
  • Ability to adjust to shifting priorities and meet timelines.
  • 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
Problem-solving
Organizational skills
Communication skills
Detail-oriented
Team player

Education

Associate degree

Tools

Microsoft Office

Job description

Canfield Scientific, Inc. is seeking a Clinical Project Associate to provide project management and operational support for designated clinical projects. The role involves ensuring quality, timelines, and project specifications are met, while aiding in documentation and supply shipments to study sites.

The ideal candidate has an associate degree or at least 1 year of experience, strong Microsoft Office skills, and excellent time management and teamwork abilities in a fast-paced environment.

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