Alliance Clinical Network · 4 months ago
Senior Clinical Research Coordinator
Alliance Clinical Network is seeking a Senior Clinical Research Coordinator to partner with the Regional Site Director and ensure compliance and productivity of clinical site staff. The role involves managing clinical trials, training staff, and overseeing various site visits while ensuring adherence to study protocols.
Hospital & Health Care
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
Qualification
Required
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
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
Preferred
2+ years' experience working as a Clinical Research Coordinator, preferred
Benefits
401 (k) Retirement Plan
Medical, Dental, and Vision Insurance
Paid Time Off (PTO)
Floating Holidays
And more!
Company
Alliance Clinical Network
For more than a decade, Alliance Clinical Network's fully integrated, wholly owned and operated clinical research sites have helped advance human health by delivering exceptional clinical trial data gathered from a proprietary, ready-to-tap, group of >250,000 diverse participants.