Martinsixtus Ezejimofor , Mem, Mph, Phd. Email & Phone Number

London, United Kingdom

• Coordinating guideline development group (GDG) meetings for clinical conditions • Coordinating pre- and post- meetings preparations relating to protocols, evidence presentation, recommendations, guideline drafting and manuscript approvals • Designing and planning for systematic review element of guideline development• Performing literature search in different databases and critical appraisal for research• Conducting study screening, data abstraction and extraction with respect to PICO• Carrying out data cleaning, synthesis and meta-analysis using appropriate statistical software • Preparation of GRADE evidence profile using GRADEpro• Presenting review evidence in meetings and workshops• Taking minutes and drafting live recommendation during GDG approval meetings• Assisting in drafting guidelines by linking evidence to recommendation (LETR)• Contributing to guideline manuscript preparation, publication, scoping and update• Training and mentoring associate systematic reviewers, analyst and other scientists • Carrying out quality control checks on BAD products including guidelines, PILS and manuals• Contributing to relevant pages of the BAD website

Coventry, United Kingdom

· Conducting systematic review and meta-analysis (Pairwise/Proportion/IPD)· Conducting network meta-analysis using STATA· Contributing to the appraisal of HTA (Single and Multiple technology appraisals) submissions · Providing specialist assistant in case-based learning (CBL)· Supporting learning activities by working alongside other lectures· Conducting a systematic review of diagnostic assessments (DAs) and other review processes· Contributing to methodological research and quality control processes for reviews· Preparation of grant proposals· Performing literature search and critical appraisal using Cochrane risk of bias tool· Performing of data cleaning and analysis as appropriate· Preparation of manuscript and review report· Helping in lecture planning and preparation of teaching materials· Contributing to student’s personal development, examination invigilation and mentoring

London, United Kingdom

· Coordinating routine staff/client meetings and presentations as appropriate· Conducting literature review to identify important advances in drugs and medical devices· Providing advice to prospective companies on regulatory product registration and licensing· Initiating relevant partnership arrangements for project implementation and franchising· Designing training needs in areas of food and drug safety, and regulation· Providing specialist advice on health intelligence issues including an analysis of specific datasets· Grant and business proposal writing and advise· Writing reports and specific proposals

Lagos, Nigeria

· Appraising critically and reviewing scientific data for drug quality and efficacy· Responding to regulatory requirement queries and specific request clearly and accurately· Issuing of import and export authorization for medicine, cosmetics and other FMCGs· Documenting adverse drug reactions (ADRs) and food allergen complaints by consumers· Issuing of compliance directives to prospective clients on product registration· Inspecting of regulatory product manufacturing establishments to ensure GMP compliance· Contributing to the agency’s regulatory information database available to the public· Reviewing/approving of clinical trial research documents for product registration and licensing· Establishing collaboration with institutions for drug and medical devices registration and licensing· Training and supervision of community survey workers· Writing report, briefing papers and record keeping

Port Harcourt, Nigeria

· Developing, updating and reviewing SOPs and analytical manuals· Validating of analytical procedures and processes for quality assurance· Liaising with relevant stakeholders on tracking of fake and adulterated regulatory products· Designing of analytical protocol for samples (water/soil) undergoing forensic investigation· Reviewing “out-of-specification” results and conducting a statistical evaluation· Auditing of laboratory equipment· Carrying out of various surveys and surveillance activities· Writing report, briefing papers and record keeping· Monitoring and evaluation of relevant data· Training of volunteers, interns and new staff on regulatory affairs and product testing

Doctor Of Philosophy (Ph.D.), Health Sciences

Master Of Philosophy (Mphil), Toxicology And Pharmacology

Master In Public Health (Mph)

Masters In Environmental Management (Mem)

Bachelor’S Degree, 2.1