Benjamin Reitz Email & Phone Number

Millcreek, Utah, United States

• Organize and prepare clinic specific meetings, site initiation visits and monitoring visits in cooperation with the data entry staff.• Manage the closing of the clinical conduct of the study by coordinating restitution and/or storage of study materials, equipment and documents and study evaluation.• Manage the clinic floor by answering questions, helping with setup, modifying schedules, etc.• Provide support in reviewing and assessing protocol, clinic budget, case report forms… Show more • Organize and prepare clinic specific meetings, site initiation visits and monitoring visits in cooperation with the data entry staff.• Manage the closing of the clinical conduct of the study by coordinating restitution and/or storage of study materials, equipment and documents and study evaluation.• Manage the clinic floor by answering questions, helping with setup, modifying schedules, etc.• Provide support in reviewing and assessing protocol, clinic budget, case report forms, informed consent forms and volunteer information. • Coordinate availability of study materials and equipment, creation of corresponding instructions, validation and verification of testing new equipment and approval of invoices. • Prepare and maintain clinical documents. Monitor submission of documents to the Institutional Review Board (IRB). Show less

Millcreek, Utah, United States

• Support the recruitment and enrollment of qualified volunteers for clinical drug trials through the review and analysis of relevant data and protocol requirements.• Maintain the feasibility of a study from a recruitment point of view during the proposal phase and communicates findings as appropriate.• Implement changes in protocol inclusion and exclusion to optimize recruitment. • Support the project team by consolidating training materials for the recruiting and screening… Show more • Support the recruitment and enrollment of qualified volunteers for clinical drug trials through the review and analysis of relevant data and protocol requirements.• Maintain the feasibility of a study from a recruitment point of view during the proposal phase and communicates findings as appropriate.• Implement changes in protocol inclusion and exclusion to optimize recruitment. • Support the project team by consolidating training materials for the recruiting and screening departments .• Reviewing the recruitment and screening outcome throughout the study to ensure that full groups are dosed according to the timelines. Show less

Millcreek, Utah, United States

• Conduct research assessments, blood draws, IV Placement, Vitals and ECG capture, urine collection and dose witness• Remain up to date with protocols, amendments, records of training and delegation logs• Document data and adverse events & QC all recordings• Screen potential subjects to determine eligibility. Explain informed consent form, and record medical history• Lead studies which include supervising assessments on the floor, resolving queries, catching deviations, managing… Show more • Conduct research assessments, blood draws, IV Placement, Vitals and ECG capture, urine collection and dose witness• Remain up to date with protocols, amendments, records of training and delegation logs• Document data and adverse events & QC all recordings• Screen potential subjects to determine eligibility. Explain informed consent form, and record medical history• Lead studies which include supervising assessments on the floor, resolving queries, catching deviations, managing follow up visits, updating subject stipends Show less