Clinical Project Associate — Imaging Trials and Data Fidelity

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

Job summary

Canfield Scientific, Inc. is seeking a Clinical Services: Clinical Project Associate to provide project management and operational support to designated clinical project teams, ensuring quality, timelines, and specifications are met.

The role involves document management, ensuring accuracy of study records, and assisting with data queries, database setup, updates, and coordination with study sites. A strong Microsoft Office proficiency and time management are essential.

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 deadlines.
• Detail oriented, flexible, and team-oriented.
• Medical device terminology and photography experience is advantageous.
• HIPAA/GCP guidelines knowledge is a plus.

Responsibilities

• Provide project management and operational support to the 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

Prioritization

Teamwork

Attention to detail

Education

Associate degree

Tools

Microsoft Office

Job description

Canfield Scientific, Inc. is seeking a Clinical Services: Clinical Project Associate to provide project management and operational support to designated clinical project teams, ensuring quality, timelines, and specifications are met.

The role involves document management, ensuring accuracy of study records, and assisting with data queries, database setup, updates, and coordination with study sites. A strong Microsoft Office proficiency and time management are essential.