Clinical Trial Associate Consultant - Onsite in NJ

A global pharmaceutical company is seeking a Clinical Trial Associate Consultant to coordinate trial activities and manage study materials. This contract role requires a Bachelor's degree and 5+ years of relevant experience. Responsibilities include scheduling meetings, reviewing study documents, and monitoring study progress. Ideal candidates will have strong attention to detail, good communication skills, and familiarity with trial management systems. This position requires onsite attendance 3 days a week in New Jersey. #J-18808-Ljbffr