Joseph Mide, Msc. Email & Phone Number

United States

United States

* Manage all aspects of clinical trials, specifically, study vendor management, including CRO oversight, and other study providers involved in clinical trial.* Support cross-functional study execution team in support of study deliverables with a focus on Clinical Operations deliverables to the study team.* Support delivery of study milestones and ensure accurate tracking and reporting of study metrics and timelines to leadership.* Ensure clinical trials are manage and execute in accordance with ICH GPC, regulations, protocols, and company-specific SOPs.* Assist in preparation and review clinical trial documentation including, but not limited to, Protocol, Informed Consent, Clinical Monitoring Plan, Project Plan, Case Report Forms, Clinical study reports, and other study-level documents.* Triage CRO and clinical site questions.* Facilitate cross-functional study team meetings and delegated follow-ups to CRAs, as appropriate; liaised with other cross-functional areas for oversight of clinical study activities. Ensure that the Trial Master File (TMF) is set up and maintained appropriately throughout the trial, including periodic reviews of patient care, safety risk management, and facility maintenance.

United States

* Led Global Clinical team, accountable for the achievement of milestones and quality of the contracted scope.* Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.* Assessed records of each patient, reviewed databases, and checked referrals to locate potential research study participants.* Monitored subject enrolment and tracked dropout details.* Collected, processed, and delivered specimens from trial participants.

United States

* Performed pre-study, closeout, and interim visits to check on study activities.* Evaluated proof of eligibility and consent for participants.* Reviewed site regulatory binder to check collection procedures and completeness of paperwork.* Discussed prerequisites to maintain team productivity for project goals and objectives.

United States

* Performed monitoring visits and tracking of study progress, thereby contributing to the overall management of clinical trials in accordance with ICH-GCP and applicable local regulations and Standard Operating Procedures (SOP).* Managed clinical study start-up, maintenance, and closure activities including maintenance of study documents. * Interfaced with sponsor representatives and the study team to ensure the timely initiation and completion of clinical trials.* Assisted with the preparation, review, and submission of all relevant regulatory documents to the appropriate Regulatory Authorities and IRB/IEC

United States

* Achieved project-specific quality and performance standards and provided documentation and communication.* Attended investigator meetings to provide a framework for successful research studies by establishing responsibilities.* Supported quality control program by scheduling site assessment visits for the project and conducting monitoring visits. * Performed pre-study site evaluations, site initiations, interim monitoring and study close-out visits while collecting regulatory documentation.* Developed protocols and case report forms .

United States

* Kept patient care protocols and clinical trial operations in compliance.* Assessed records of each patient, reviewed databases, and checked referrals to locate potential research study participants.

Master Of Science - Ms, International Tourism Management.

Higher National Diploma, Tourism And Hospitality Management.