Eugene Akahoho Email & Phone Number

New York, Ny, Us

New York, Ny, Us

Raritan, New Jersey, Us

Eugene currently holds the position of Senior Clinical Monitor performing Site Management Services for PRAHS Global Clinical Operations and providing services for Janssen Research & Development in Clinical Pharmacology and Early Phase Development. As a Site Manager, he serves as the primary contact with sites, performs sites visits from initiation to close-out, and evaluates and ensures patient safety, data quality and integrity, adherence to the protocol and agreed SOPs. He also serves as a mentor for junior level CRAs and serves as a resource for new employees.

The SUNY At Albany Alumni Association is the umbrella organization for all University alumni. Its purpose is to build and sustain a lifelong relationship between the University and its alumni through the following activities:- Fostering leadership among alumni from all schools, regions and constituencies- Engaging students as future alumni- Providing opportunities for lifelong learning for alumni- Recognizing alumni for accomplishments and service- Providing social and career networking for alumni- Supporting alumni organizations, regional groups, constituency groups and students- Encouraging participation of schools in UA Alumni Association activities- Facilitating the sharing of ideas between school associations- Providing an avenue for feedback to the administration - Supporting the Fund for the University (annual giving)

Durham, North Carolina, Us

Eugene holds the position of Sr. Clinical Research Associate in Oncology and Acute Care at IQVIA Biopharmaceuticals Health Partnerships in collaboration with Lilly Integrated Clinical. As a Sr. CRA, he serves in several mentoring capacities for incoming CRAs. He also serves as the primary contact with sites, performs sites visits from initiation to close-out, and evaluates and ensures patient safety, data quality and integrity, adherence to the protocol and agreed SOPs to maintain compliance and inspection readiness.

New York, Ny, Us

Coordinating, leading and performing clinical data management activities for Institute Initiated studies in accordance with office SOPs and policies, Working with research team to implement standards for research protocol management, policies and procedures in the Macrobead group, Preparing study detailed documents for monitoring visits, Conducting QA and QC internal audits for phases I and II trials, Preparing documents for IRB submission and renewals and terminal reports, Preparing documents such 1571, 1572 and Type C meeting package for the FDA, Working with research team to prepare Clinical Study Report (CSR), Investigator’s Brochure (IB) and FDA Annual Reports

As a CRA, he serves as the primary contact with sites, performs sites visits from initiation to close-out, and evaluates and ensures patient safety, data quality and integrity, adherence to the protocol and agreed SOPs.

- Ensuring that programs are being efficiently run and that the staff is fulfilling their responsibilities- Motivating employees by being inspiring and remaining optimistic even when challenges are being faced. - Encouraging good performance and values - Allocating resources and supplies to the staff in order to make sure they have the correct equipment to complete their responsibilities to the highest potential. - Making sure that programs and activities are being laid out efficiently and as effectively as possible. Ensure that the activities implemented are of good quality and relevant to the mission and vision of the organization. - Advocating and embracing development- Being a leader by setting high standards and living by these standards, mentoring and instilling hope in coworkers and followers, and making hard decisions and critical choices.- Hiring and managing the organization and staff

A fellowship of Pastors:- Strategic Consulting, including business plan- Generating new development- Comprehensive database management and communication

Performed clinical data management activities for assigned studies in accordance with office’s SOP and policies, Oversee the Clinical Trial Management System (CTMS) of Phase 1 through Phase 3 Melanoma industry sponsored and investigator initiated trials such as Inform, Medidata, and Infoed databases, Worked with a team of 3 research coordinators to implement standards for research protocol management, policies and procedures in the Melanoma group, Assisting with study protocol development, maintenance and implementation, Prepared study detailed documents including consent forms and case record forms, Managed about 10 active and long-term follow up trials, Prepared documents for IRB submission and renewals and terminal reports, Conducted Internal study audits, Coordinate specimen collection, processing, storage, and shipment for clinical research trials

Ongoing management of Phase 1 through Phase 3 lung, ovarian, colorectal, pancreatic and neuroendocrine studies according to site/sponsor/IRB guidelines, Responsible for patient screening, recruitment, consent process and enrolment for ongoing clinical research projects, including all follow up management visits, Coordinated, lead and performed clinical data management activities for about 15 assigned studies in accordance with office’s SOP and policies and practices, Maintained source documentation and drug/device accountability, Conducted specimen collection, processing, storage, and quality control for clinical research studies, Worked with Industry sponsored, Investigator Initiated, CALGB and ECOG studies

Master Of Public Health - Mph, Health Policy And Manageme

Executive Leadership Certificate, Clinical Research

International Business

Post-Baccalaureate, Pre-Medicine/Pre-Medical Studies

Bachelor’S Degree, Human Biology

Master’S Degree, Health Policy And Management