Clinical Project Coordinator: Fast-Paced Data & Study Ops

Canfield Medical Imaging; Parsippany-Troy Hills (NJ); On-site; USD 31,684 - 38,572; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with employer match (50%)

Paid time off

Job summary

Canfield Medical Imaging in Parsippany, NJ, seeks a Clinical Project Associate who can prioritize, multitask, and communicate effectively in a fast-paced environment. You will provide project management and operational support to the designated clinical project team, manage study documentation, assist with data queries, QC checks, and communications with study sites.

Required: associate degree or 1 year experience; proficient in Microsoft Office; strong time management, problem‑solving, and

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

Communication

Multitasking

Teamwork

Education

Associate degree or 1 year work experience

Tools

Microsoft Office

Job description

Canfield Medical Imaging in Parsippany, NJ, seeks a Clinical Project Associate who can prioritize, multitask, and communicate effectively in a fast-paced environment. You will provide project management and operational support to the designated clinical project team, manage study documentation, assist with data queries, QC checks, and communications with study sites.

Required: associate degree or 1 year experience; proficient in Microsoft Office; strong time management, problem‑solving, and