Senior Clinical Research Coordinator

Job Description

Job Description

60% Travel is Required for this Position

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.

QUALIFICATION REQUIREMENTS :

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.

EDUCATION AND EXPREIENCE :

WORK LOCATION : Irving, Texas

TRAVEL INVOLVED : 60%

BENEFITS :