Sarah Noah Email & Phone Number

United States

Acts as lead contact for regional and or/project matters. Responsible for owning and achieving interim and final contractual deliverables according to the time, quality/scope and cost constraints.

Acts as lead contact for regional and or/project matters. Understands/manages/satisfies client contractual, organizational and relationship needs/expectations.

Primary liaison with client, vendors, and other PRA functional areas. Owner of all contract deliverables; Ensures that all project tasks meet client and PRA expectations, and are delivered in accordance with the contract, trial protocol, ICH-GCP, applicable SOPs and applicable regulatory requirements.

Noblesville, In

Manager of Clinical Operations team acting as Lead CTM, Globally within the project level and execution of all clinical deliverables per the project contract and specifications.

Indianapolis, Indiana Area

Manager of Clinical Operations team acting as Lead CTM, Globally within the project level and execution of all clinical deliverables per the project contract and specifications.

Indianapolis, Indiana Area

Manager of Clinical Operations team at the project level and execution of all clinical deliverables per the project contract and specifications.

Indianapolis, Indiana Area

Indianapolis, Indiana Area

• Maintain, prepare and submit regulatory documents.• Responsible for recruitment, screening, and clinical assessment of patients including vitals, phlebotomy, study assessments and lab processing.• Ensure compliance with Good Clinical Practice guidelines.• Accountable for completion of source documents, CRF entries, and SAE reporting.• Responsible for identifying protocol deviations and ensuring protocol compliance to sponsor and IRB.• Manage patient/subject scheduling, appointments, and data.• Maintain drug accountability logs, dispense/collect medication, and asses patient compliance.

• Coordinate Research and grant initiatives.• Prepare and submit regulatory documents.• Responsible for recruitment, screening, and clinical assessment of patients including vitals, ECG’s, phlebotomy, study assessments and lab processing.• Ensure compliance with Good Clinical Practice guidelines.• Accountable for completion of source documents, CRF entries, and SAE reporting.• Responsible for identifying protocol deviations and ensuring protocol compliance to sponsor and IRB.• Manage patient/subject scheduling, appointments, and data.• Negotiate budgets, maintain invoicing and regulatory documentation.• Maintain drug accountability logs, dispense/collect medication, and asses patient compliance.