Clinical Research Microsoft Office

SAMUEL O. OJO, DVM, MVPH

***** ********* **, ******* **. 30228

PHONE: 678-***-****, EMAIL: *********@*****.***

Highlights:

Over 3 years of Clinical Research Monitoring Experience

Experienced in phases I, II, III, IV.

Experienced in implementation of regulatory guidelines of ICH-GCP, study Protocols, FDA and IRB.

Experienced in handling and shipping of infectious specimens & performing EKG, CPR & Phlebotomy. Therapeutic Experience:

Infectious Disease: HIV, Influenza, Tuberculosis

Endocrinology: Type 2 Diabetes, Obesity.

Musculo-skeletal: Rheumatoid Arthritis, Aging/ Senescence, Osteoarthritis, Bone fracture.

Cardiovascular: Hypertension, Heart failure.

Experience:

Qatar Biomedical Research/ Hamad Medical Cooperation, Qatar CRA I July 2013-Present

Conducted feasibility/ pre-study, initiation, routine monitoring, and closeout visits at investigator sites.

Ensured completeness, submissions and regular updates of regulatory and ethical documents.

Coordinated study material shipment and receipt at study sites.

Routinely performed SDV, IP accountability and regularly reviewed ICF, CRFs and Regulatory binder.

Assisted study coordinator to prepare and process SAEs reports and timely resolved site queries.

Performed site monitoring visits to ensure total adherence to ICH-GCP guidelines, study protocol and conducted training and re-training as required to site staffs.

Conducted final close-out visit and archiving of all study documents and wrote reports. Canadian Veterinary Hospital, Doha Qatar Veterinary Nurse/Tech January 2011- June 2013

Perform routine lab procedures and analyses in hematology, microbiology, urinalysis and serology.

Perform catheterization- urinary//venous and analyzed skin and ear cytology and other radiographic and diagnostic procedures..Induce and monitor patients under anesthesia and assisted in surgical procedures.

Take and record vital signs and ensured appropriate infection prevention and control measures. National Tuberculosis Research Center, University of Ibadan, Nigeria, (CRA1) Sept. 2009 – Dec. 2010

Participated in the recruitment and screening of potential study subjects and obtaining Inform Consent.

Ensured that clinical study activities were conducted according to study protocol and SOPs,in compliance with all applicable laws and regulatory guidelines of ICH-GCP and HIPPA.

Maintained database information of all subjects, organize CRFs, Regulatory binder and receipt of IP and shipment of biological specimens.

Resolved queries on CRF data with study personnel and ensured safety reporting.

Reviewed TMF and maintained correspondence with IRB on AEs, renewals and protocol amendments .

Developed budget for the clinical trial and ensured all materials were available to subjects.

Attended investigators meetings and Performed Close-out visit and wrote reports. National FADAMA Agric Development Project, Nigeria Facilitator/field officer Jan. 2006-May 2009

Managed the accurate data entry and queries, data integrity, security and confidentiality

Facilitated and trained cohorts of existing and potential FADAMA User Groups (FUG).

Disseminated information on best practices for FUG to improve farm productivity.

Liaised between FUG & government to ensure improved production, storage, handling & transportation.

Prepared local development plans and implementation strategies.

Provided classroom lectures and training on scientific advances in agriculture and animal breeding.

Provided supportive supervision and technical assistance to FUG on how to prepare local developments. Education/Certifications:

University of Ibadan, Nigeria Master of Veterinary Public Health (MVPH) September, 2008

University of Ibadan, Nigeria Doctor of Veterinary Medicine (DVM) April, 1994

Knowers Training Institution Foundations in Trial Monitoring/ ICH-GCP July, 2012.

Occupational Safety and Health Professional (OSHA) September, 2011

EU funded workshop for Field surveillance officers on Surveillance & monitoring trial. Nov. 2007.

World bank funded workshop for FADAMA Project Facilitators & Field officers. Jan.2006 SKILLS.

Proficient in Microsoft Office/Servers, Apple work: Word, page, Excel, Numbers, PowerPoint/Keynote.

Electronic Data Capture: OCRDC, Data labs and inform and CTMS Impact.

Initiative and problem solving skill, Strong Interpersonal and Communication skills.

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