Ryan Ebersohl Email & Phone Number

Morrisville, Nc, Us

Durham, North Carolina, United States

• To liaise closely with the Data Manager to report trial progress and any issues outstanding.• To attend study update meetings or calls with the trial sponsor.• To assist the Data Manager with the preparation of trial documentation.• To assist the Data Manager to prepare and write the Data Management Plan.• To assist the Data Manager to prepare database and edit check specifications.• To perform post configuration peer review of Study Design document and database specification.• To assist the Data Manager with the creation and validation of Manual and SAS checks.• To assist the Data Manager with the reconciliation of data from external sources• To perform verification and User Acceptance Testing of configured databases.• To assist the Data Manager in all data cleaning activities.• To review SAS listings/SAS tables.• Responsible for the registration of users into the EDC/CTMS system, performing system demonstrations.• To create CRF and eCRF completion guidelines, EDC system manuals and access instructions.• To develop a detailed knowledge of assigned trials and to perform duties which are trial specific.• To assist with the maintenance of procedure logs, coding schemes, input notes and Data Entry Manuals.• To establish and/or maintain correspondence files with participating centers.• Archiving of trial documentation and (e)CRFs.

• Develop and maintain documents, tools, forms and related items in MS Word, Excel, Access and Publisher, including reformatting and troubleshooting issues with existing documents and macros• Assist Clinical Operations personnel with study initiations and special projects• Provide technical assistance to project team (Project Managers, Lead CRAs, CRAs, etc.) with forms, letters, reports, manuals and other documents• Manage document control functions, including maintaining Master List of paper and electronic documents and media generated and distributed• Audit and resolve issues of redundancy, currency and consistency of documents on shared drive and portals• Maintain and quality audit to assure most recent revisions of documents are on portals and server• Assist project team (CRAs, Lead CRAs and Project Managers, etc.) with collation of documentation required for submission to Regulatory Authorities and Ethics Committees administrative support to the preparation of contracts• Assist with maintenance of trial master file documents as appropriate and needed• In liaison with the CRAs, manage preparation of documents for grant payments• Regularly review the status of key documentation in the file for SOP compliance• Provide support to Clinical Operations Manager on an ad hoc basis.

• Perform feasibility studies/site identification activities for potential sites, as requested • Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study site • Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.) • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF) • Assure maintenance of the Investigator Site File in the TMF • Conduct pre-study, study initiation and interim monitoring visits under the guidance of the local CRA or LCRA/PM, as applicable and appropriate • Document site visit findings at site visits via written reports, under the guidance of the local CRA or LCRA/PM, as applicable and appropriate • Maintain regular communication with sites • Complete remote CRF review, using electronic data capture systems • Assist sites in query resolution • Assist with ensuring site compliance with IP receipt, accountability and return or destruction, as applicable and appropriate

• Develop and maintain documents, tools, forms and related items in MS Word, Excel, Access, PowerPoint and Publisher, including reformatting and troubleshooting issues with existing documents and VBA code• Manage document control functions, including maintaining Master List of paper/electronic documents and media generated and distributed for Clinical Operations• Assist Clinical Operations personnel with completion of study specific tasks (e.g. study initiation, and preparation of study file notebooks)• Maintain interdepartmental communication to ensure consistency and availability of new forms and revisions• Collect, review, and organize information for database entry (Site Visit Reporting)• Audit and resolve issues of redundancy, currency and consistency of Clinical Operations documents on shared drive, SharePoint and portals• Provide administrative support to Clinical Operations department• Assist in development of presentations and presentation materials• Develop and distribute periodic communication materials

Durham, Nc

• Lead Reader on multiple clinical studies in either phase 3 or 4• CRF generation, Study startup procedures, EDC experience• Assist in preparation of Reading Center publications• Grade OCT/FP/MAIA/Slit lamp for pathology/quality regarding study parameters• Assist with training and certification for study investigators, coordinators, and technicians for study data capture and submission to the Reading Center• Assisted in fellow OCT technicians certification and understanding of reading images

Cary, Nc

- Prepare and administer medications – Injections, intranasal, topical, oral, and subcutaneous are the most common.- Blood draws and testing – Assisted in drawing blood and then setting up lab work to be done locally or sent out to a testing facility- Work with clients directly by gathering histories and discussions on how to better care for patients

- Administer medications (topical, oral, subcutaneous, etc.)- Assist in Blood Draw - Assist in holding animals and preparation of syringes- Day-to-day care of animals - Including feeding, cleaning, and grooming/holding and maintenance of a clean and healthy habitat, monitoring for signs of distress