Clinical Project Coordinator

Canfield; New Jersey; On-site; USD 32,000 - 39,000; Full time

Benefits offered by this job

Paid days off

Medical, dental, and vision insurance

Discretionary bonus

401(k) plan with employer match (50%)

Job summary

Canfield Scientific, Inc. is seeking a Clinical Project Associate to provide project management and operational support for designated clinical project teams in New Jersey.

You will help ensure quality, timelines, and project specifications are met, assist with study documentation, and manage supply shipments to study sites. The ideal candidate has an associate degree or 1 year of experience, strong Microsoft Office skills, and solid time management, problem-solving, and organizational

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

Teamwork

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 project teams in New Jersey.

You will help ensure quality, timelines, and project specifications are met, assist with study documentation, and manage supply shipments to study sites. The ideal candidate has an associate degree or 1 year of experience, strong Microsoft Office skills, and solid time management, problem-solving, and organizational