Clinical Project Associate: Fast-Paced PM & Data Ops

Imagingexcellence; New Jersey; Híbrido; USD 32 000 - 39 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Paid days off

Medical insurance

Dental insurance

Vision insurance

Discretionary bonus

401(k) with employer match (50%)

Resumo da oferta

Canfield Scientific, Inc. in New Jersey seeks a Clinical Project Associate to provide project management and operational support for designated clinical project teams, ensuring quality, timelines, and project specifications are met.

The role involves database setup, maintenance, data query resolution, QC checks, and proactive communication with study sites. It requires multitasking, strong time management, and teamwork in a fast-paced environment.

Qualificações

• 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.

Responsabilidades

• 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

Conhecimentos

Time management

Communication skills

Multitasking

Organizational skills

Detail oriented

Formação académica

Associate degree or equivalent experience

Ferramentas

Microsoft Office

Descrição da oferta de emprego

Canfield Scientific, Inc. in New Jersey seeks a Clinical Project Associate to provide project management and operational support for designated clinical project teams, ensuring quality, timelines, and project specifications are met.

The role involves database setup, maintenance, data query resolution, QC checks, and proactive communication with study sites. It requires multitasking, strong time management, and teamwork in a fast-paced environment.