Job Description

Responsible for the coordination and administration of clinical trials. You will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. Responsibilities:

• Ensure the safety and welfare of study participants
• Conduct the study as per protocol, GCP, and SOPs
• Ensure all study activities are completed correctly
• Assist in local recruiting efforts for clinical trials
• Support to ensure operationally ready to achieve recruitment plans and objectives
• Lead regularly scheduled research meetings with focus on recruitment and retention, study and site updates, and ensuring engagement of CRP and Investigators
• Support site level physician engagement ensuring site recruitment and support
• Perform delegated research and administrative procedures to assist in conducting clinical studies under the direction of the Investigator
• Perform ECGs, vital signs, meal distribution, study participant monitoring, and other tasks as required by protocol/site
• Perform phlebotomy, point of care testing, sample collection, processing & shipping as required by protocol/site
• Timely and accurate completion of source, data, CRFs, queries and CTMS
• Verify input data and timely documentation regularly and accurately
• Support the review of source docs and other study documents, as required
• Support audit preparation for any site inspections
• Perform regular quality control (QC) checks and other QC tasks as deemed necessary
• Support quarterly recruitment targets and support efforts to achieve site/company KPIs

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