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Clinical Research Coordinator

Actalent

Posted Monday, June 30, 2025

Posting ID: JP-005382176

King of Prussia, PA
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Job Title: Clinical Research Coordinator


Job Description

We are seeking a Clinical Research Coordinator to perform ultrasound imaging for research participants during scheduled onsite visits. The role involves collaboration with clinical and research teams to gather, document, and manage imaging and clinical data. The coordinator will ensure accurate and timely entry of results into study databases, support patient recruitment efforts, and maintain compliance with study protocols and regulatory requirements.


Responsibilities

  • Perform ultrasound imaging for research participants during scheduled onsite visits.
  • Collaborate with clinical and research teams to gather, document, and manage imaging and clinical data.
  • Ensure accurate and timely entry of results into study databases.
  • Support patient recruitment efforts, including outreach, screening, and scheduling.
  • Maintain compliance with study protocols and regulatory requirements.

Essential Skills

  • Ultrasound certification - MUST HAVE
  • At least 1-2 years of experience in clinical research coordination
  • Strong data management skills
  • Good people skills
  • Highly organized
  • Proficient in paperwork and data entry

Additional Skills & Qualifications

  • Oncology background preferred, not required
  • BS preferred, not required (years of experience can make up for it)
  • Effective communication and organization skills

Work Environment

The position is fully onsite, requiring work five days per week in King of Prussia, PA. The coordinator will work closely with multiple teams and one Principal Investigator (PI) on the trial. The clinic focuses on a breast cancer device trial, providing an opportunity to support a high enrollment trial. Benefits include 1 week of PTO and 6 Actalent holidays.

Compensation:$35

Contact Information

Email: azajac@actalentservices.com

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
On-Site
Clinical Research
Research
Effective Communication
Data Management
Medical Ultrasonography
Clinical Research Coordination

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