In-House Clinical Research Associate II, Sponsor-Dedicated (Contract)

What you'll be doing

• Partners with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams.
• Carry out remote monitoring of clinical trials
• Serves as the secondary contact for sites supporting CRAs
• Responsible for the proper reporting and follow up of SAEs and ensures all reportable events are identified, clearly documented and reported per protocol as well as applicable requirements and regulations
• Ensures any identified non-compliance issues are addressed, clearly communicated, documented and escalated as required through monitoring visits, analyzing study metrics, and general study data overview
• Assists with audit/inspection readiness, study start-up activities, data listing reviews, monitoring visit support and issue resolution

What we are searching for

• Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
• Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience
• 3 to 5 years of practical experience in clinical trials. Alternately, a proven experience in all primary job functions
• Participate in study-specific meetings, teleconferences and training as needed
• Demonstrates excellent English verbal and written communication skills
• Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverable, and task ownership
• Preferred Location: East Coast / Central

This is a 1099 12-month contract position with the potential to extend and renew after 1 year.