Clinical Project Associate — Fast-Paced Study Ops

Imagingexcellencesymposium; Parsippany-Troy Hills (NJ); On-site; USD 32,000 - 39,000; Full time

Benefits offered by this job

Paid days off

Medical insurance

Dental insurance

Vision insurance

Discretionary bonus

401(k) with employer match

Job summary

Canfield Scientific, Inc. is seeking a Clinical Project Associate in Parsippany, New Jersey. The role involves coordinating clinical project activities, maintaining study documentation, and supporting data management to ensure timely, high-quality study deliverables.

The ideal candidate has an associate degree or at least one year of experience, strong Microsoft Office skills, and excellent time management. The position is on-site with competitive hourly pay and comprehensive benefits.

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

Team player

Attention to detail

Education

Associate degree

Tools

Microsoft Office

Job description

Canfield Scientific, Inc. is seeking a Clinical Project Associate in Parsippany, New Jersey. The role involves coordinating clinical project activities, maintaining study documentation, and supporting data management to ensure timely, high-quality study deliverables.

The ideal candidate has an associate degree or at least one year of experience, strong Microsoft Office skills, and excellent time management. The position is on-site with competitive hourly pay and comprehensive benefits.