Clinical Services: Clinical Project Associate

Canfield Scientific; Köln; Vor Ort; EUR 40.000 - 70.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Clinical Project Associate to support clinical project teams in a dynamic environment. This role involves managing project documentation, ensuring quality and timelines are met, and maintaining databases. The ideal candidate will possess strong time management and communication skills, thrive in a fast-paced setting, and be detail-oriented. Join a leading company that supports global clinical trials and be part of a team that sets the gold standard in clinical imaging and data quality. If you are ready to make a significant impact in the healthcare industry, this opportunity is for you.

Qualifikationen

• Associate degree or 1 year work experience required.
• Proficiency in Microsoft Office is essential.

Aufgaben

• Provide project management support to clinical project teams.
• Manage study documentation and ensure accuracy.
• Perform quality control checks to maintain data integrity.

Kenntnisse

Time Management

Problem-Solving

Communication Skills

Organizational Skills

Detail Oriented

Ausbildung

Associate Degree

1 Year Work Experience

Tools

Microsoft Office

Jobbeschreibung

Clinical Services: Clinical Project Associate

An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong communication skills. The right individual will have strong time management skills and works well in a fast-paced environment.

Job Description:

• 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

Core Requirements:

• 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

Desired Requirements:

• Medical device/medical terminology and photography experience is advantageous
• HIPPA/GCP guidelines knowledge is a plus

Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Canfield has supported over 3,200 clinical studies, works worldwide with thousands of clinical study sites, and has been retained by many of the world's leading biotechnology and pharmaceutical companies. Canfield's imaging equipment leads the industry providing high-quality, registered, reproducible clinical images. This, together with proactive clinical image monitoring and a world class quality assurance regimen, sets the gold standard in image quality for clinical studies.

Apply Here

Please submit resumes with cover letter to [e-mail] or click below for immediate consideration. Please include the position title in the subject line.

We are proud to be an equal opportunity employer.