Clinical Research Associate (Park Ridge, NJ)

Primary Responsibilities:
-Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments
-Assist in the management of the Trial Master File (submit documents, reconciliation, QC, etc.)
-Participate in development of protocol, case report form, CRF guidelines and other study documents
-Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal
-Reviews and approves monitoring reports and ensures tracking of ongoing site issues

Qualifications:
-Bachelor's degree in relevant scientific discipline
-Minimum 3-5 years exp in a pharma company (large pharma preferred)
-Experience in phase 3 global study trials in multifunctional areas
-Must have experience in reviewing patient data and patient profiles
-Oncology experience is highly preferred

Type: Long-term Contract