Posted in Other 30+ days ago.
Type: Full Time
Location: Camden, New Jersey
SHORT DESCRIPTION
Assists the Principal Investigator and other members of the research team with preparation
of IRB protocols, consent forms, and development of study budget.
Completes and maintains all study documents as required.
Assists with the identification and recruitment of study participants.
Work as a team player with all involved in the studies.
SPECIAL REQUIREMENTS
MINIMUM QUALIFICATIONS
High School Diploma or Equivalent required.
0-2 years research experience.
Medical Assistant, LPN or Phlebotomist experience preferred.
Required License/Certifications/ Registration:
Other Qualifications: Basic understanding of Microsoft Excel, Outlook and Word.
Scheduled Days / Hours: M-F 8:30a-5:00p