Clinical Research Coordinator - Entry Level, Flexible Hours

kozmetickesluzby.vecnakraska.sk - Jobboard

Philadelphia (Philadelphia County)

On-site

USD 43,888 - 44,947

Full time

14 days+
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Benefits offered by this job

Health, Life, and Flexible Spending Accounts
Tuition assistance
Retirement plans
Wellness resources

Job summary

The Perelman School of Medicine is seeking an entry-level Clinical Research Coordinator A to support faculty and clinical research staff in the Department of Medicine. This position primarily focuses on the rare disease Fibrodysplasia Ossificans Progressiva (FOP) and entails various research responsibilities.

The ideal candidate should hold a Bachelor of Science degree, demonstrate attention to detail, and possess effective data entry skills. Responsibilities include ensuring participant safety, assisting with clinical assessments, and managing regulatory submissions.

Qualifications

  • 1 to 2 years of experience or equivalent combination of education and experience is required.

Responsibilities

  • Complete onboarding and maintain necessary training for clinical research.
  • Collect and enter data accurately with low query rates.
  • Assist with clinical assessments and specimen handling.
  • Interact with patients and document adverse events appropriately.
  • Participate in monitoring visits and assist with regulatory submissions.

Skills

Attention to detail
Data entry accuracy
Patient interaction

Education

Bachelor of Science

Job description

The Perelman School of Medicine is seeking an entry-level Clinical Research Coordinator A to support faculty and clinical research staff in the Department of Medicine. This position primarily focuses on the rare disease Fibrodysplasia Ossificans Progressiva (FOP) and entails various research responsibilities.

The ideal candidate should hold a Bachelor of Science degree, demonstrate attention to detail, and possess effective data entry skills. Responsibilities include ensuring participant safety, assisting with clinical assessments, and managing regulatory submissions.

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