Senior Clinical Research Coordinator - 119425

Senior Clinical Research Coordinator

Overview

• Full-time / Direct-hire
• On-site

Essential Duties and Responsibilities

• Partner with Regional Site Director to ensure compliance and productivity of all clinical site staff and operations.
• Manage, train and support clinical site staff.
• Review, comprehend and communicate study protocols.
• Oversee Site Initiation Visit (SIV), Pre-Study Validation Visit (PSV) and Interim Monitoring Visit (IMV).
• Assist CRC team as requested to facilitate research and business needs.
• Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOP’s.
• Ensure all data is entered into sponsor’s data portal and all queries are resolved in a timely manner.
• Work closely with CRO/CRA and IRB.
• Perform administrative tasks such as ordering supplies and equipment for the study.
• Manage all required study start up documentation, training and timelines on assigned study protocols.

Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• Associate’s degree and/or completion of accredited healthcare certification program, required.
• Comfortable stepping into a leadership role.
• 2+ years’ experience in clinical research, required.
• 2+ years’ experience working as a Clinical Research Coordinator, preferred.
• Comprehensive knowledge of FDA, GCP & confidentiality.
• Exceptional attention to detail and organization.
• Excellent written and communication skills.
• A proven ability to multi-task in a rapidly changing environment.

Benefits

• 401(k) Retirement Plan
• Medical, Dental, and Vision Insurance
• Paid Time Off (PTO)
• Floating Holidays
• And more!