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Clinical Research Coordinator



Posting ID: JP-002018795

Full Time
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Clinical Research Recruiter

Philadelphia, PA


  • Recruit, screen, and enroll subjects to clinical trials
  • Explain Informed Consent process
  • Document adverse events
  • Collect study documents, protocols, regulatory documents, informed consents, and case report forms
  • Prepare the IRB/IRB applications


  • BA/BS
  • 1-3 + years experience
  • Experience in adverse event reporting
  • Experience with patient recruitment/consenting
  • Effective communication and writing skills
  • Knowledge of IRB

About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at

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.

Contact Information

Recruiter: Stephanie Curran

Phone: (610) 232-5803


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