Over 10 years we help companies reach their financial and branding goals. Maxbizz is a values-driven consulting agency dedicated.

Gallery

Contact

+1-800-456-478-23

411 University St, Seattle

maxbizz@mail.com

Organizational Structure

CEO

The Chief Executive Officer (CEO) is the highest-ranking executive at Gulapro Limited. The CEO is responsible for defining the strategic vision, making major corporate decisions, and acting as the main liaison between the board of directors and operations. Key roles include setting company culture, allocating resources, managing performance, and representing the firm to external stakeholders.

Director

Gulapro Directors are fiduciaries responsible for promoting the company's success, acting in good faith, and exercising independent judgment. The Directors ensure legal compliance, manage conflicts of interest, and exercise reasonable care, skill, and diligence. Key duties include filing financial accounts and maintaining solvency

Human Resource (Administration)

HR office at Gulapro handle hiring, training, and supporting staff. HR office help staff develop in their jobs and improve workplace life

Business Development Lead (Commercial Division)

Business Development Lead at Gulapro Limited drives company growth by identifying new markets, building strategic partnerships, and acquiring clients. Responsibilities include strategic planning, sales pipeline management, conducting market research, and negotiating contracts to meet revenue targets. They lead initiatives for long-term expansion and collaborate with marketing/sales teams.

Financial Officer/Accountant (Administration)

Financial Officer/Accountant at Gulapro Limited manages all financial transactions, ensures compliance, and prepares financial reports (balance sheets, P&L statements). Key roles include managing cash flow, overseeing ledgers, handling tax returns, and budgeting. The Finance Officer also provide financial analysis to management to support strategic decisions and ensure data confidentiality.

Pharmacist Lead (CRSS Division)

Pharmacist Lead at Gulapro Limited play a crucial role in healthcare by ensuring the safe and effective use of medications, providing patient education, and collaborating with healthcare teams.Key Responsibilities of Pharmacists include:Dispensing Medications,Patient Counseling,Medication Management,Health Screenings and Immunizations and Professional Collaboration: Pharmacists work closely with physicians, nurses, and other healthcare professionals to support patient care and improve treatment outcomes. They provide valuable insights regarding medication management and safety

Regulatory Specialist (CRSS Division)

Regulatory Specialist at Gulapro Limited manages the regulatory compliance, documentation, and submission processes for clinical trials, ensuring adherence to FDA, GCP, and IRB guidelines. The RS facilitate study start-up, maintain essential documents, submit amendments, and handle safety reporting. Key Responsibilities include Regulatory Submissions, Documentation Management, Compliance Monitoring, Safety Reporting, Study Oversight and Communication

Clinical Research Support Services Lead (CRSS Division)

Clinical Research Support Services Lead at Gulapro Limited manages the operational, logistical, and quality assurance aspects of clinical trials, providing leadership to support staff to ensure studies are conducted in compliance with regulatory standards

Health Systems Strengthening Lead (HSS Division)

Health Systems Strengthening (HSS) Lead at Gulapro Limited provides strategic, technical, and managerial leadership to improve health system components—such as governance, financing, workforce, and service delivery

Accreditation Lead ( Lab/QMS Division)

ISO Accreditation Lead at Gulapro Limited is responsible for driving the planning, execution, and reporting of audits to assess an organization's management system against international ISO standards

Clinical Research Associate(CRSS Division)

Clinical Research Associate (CRA) at Gulapro Limited monitors clinical trials to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements. They manage site initiation, monitoring, and close-out visits, verify data integrity, protect participant safety, and act as the primary liaison between sponsors and clinical sites

Laboratory Specialist (Lab/QMS Division)

Laboratory Specialists at Gulapro Limited performs, analyzes, and oversees complex laboratory tests, experiments, and diagnostics to support medical, industrial, or research objectives. Key duties include operating and calibrating equipment, maintaining rigorous quality control, managing inventory, adhering to safety protocols, and ensuring regulatory compliance

Quality Management Systems Specialists (Lab/QMS Division)

A Quality Management System (QMS) Specialist at Gulapro Limited develops, implements, and maintains organizational quality standards (e.g., ISO 9001, IATF 16949) to ensure compliance and continuous improvement. They conduct internal audits, manage corrective actions (CAPA), document procedures, and analyze performance data to enhance operational efficiency, safety, and product quality

Primary Healthcare Lead (CRSS Division)

Primary Healthcare (PHC) Lead at Gulapro Limited directs, manages, and provides technical oversight for primary care projects, aiming to improve service delivery, quality, and access to care. They develop strategies, mentor staff, monitor budgets, and foster partnerships with local stakeholders to achieve health targets

Community Healthcare Lead (CRSS Division)

Community Healthcare Lead at Gulapro Limited manages local health services, coordinating care and leading multidisciplinary teams to deliver patient-centered services. Key responsibilities include facilitating communication between patients and providers, leading service planning, implementing clinical initiatives, conducting risk assessments, and representing GP practices in community networks

Office Assistant Lead (Administration)

Office Assistant Lead at Gulapro Limited coordinates daily administrative operations, managing front-desk coverage, scheduling, and correspondence while supervising junior support staff. Key duties include maintaining office supplies/equipment, filing, and providing high-level clerical support to enhance office efficiency. This role requires strong communication, organizational skills, and proficiency in MS Office

Adhiambo Opondo-Asiyo

Health Information Advocate and Acting CEO

Tonie Konig

Co-Founder CTO PTC Gulapro Limited-Strategic Partner

Evans Odipo
Diploma in Clinical Medicine and Surgery; Bachelor of Science in Community Health and Development

Senior Regulatory
Specialist (CRSS Division)

Dr. Momanyi Ogeto

Dr. Momanyi Ogeto
Bachelor of Medicine and Bachelor of Surgery (MBChB

Clinical Research Support Services Lead (CRSS Division), Acting Director

Susan Musau
BSc, MSc, PhD-cont’d

Laboratory, Quality and Accreditation Lead
(Laboratory/Quality Management Systems Division)

Nondi Akombo Moses
Diploma and Bachelor’s Degree in Clinical Medicine and Surgery; MSc Clinical Research-cont’d

Senior Clinical Research Associate (Clinical Research Support Services Division)

Judith Adhiambo Owino
Bachelor of Science in Applied Statistics with IT). Statistician (Health Systems Strengthening Division

Senior Statistician (Health Systems Strengthening Division)

Andrew Yego
BSc, MSc, BPharm-cont’d

Pharmacology
(Health Systems Strengthening Division)

Damaris Juma Okiri
Diploma Community Health Nurse, Bachelor of Science in Nursing, Masters in Epidemiology and Biostatistics-cont’d

Senior Clinical Research Associate (Clinical Research Support Services Division)

Felix O. Adundo
Bachelor of Science in Applied Statistics and Computing, Master of Electronic Information

Senior Clinical Research Associate (Clinical Research Support Services Division)

Charles Kato

Charles Kato
Diploma in Clinical Medicine and Community Health; BSc in Medical Imaging Graduate Degree-cont’d

Senior Clinical Research Associate (CRSS Division) and Representative for Uganda

Dr. Busolo Nicholas
PhD, CHRP, MBA, PGD HRM, BED, MKIM.

Business Development Lead (Commercial Division)

Victor Omondi

Victor Omondi
BSc, MSc

Health Systems Strengthening Lead (HSS Division)

Brenda Misiko
Diploma, Clinical Medicine & Surgery; BSc. Public Health & IT - Maseno University; MSc. Epidemiology and Biostatistics-cont'd

Senior Clinical Research Associate (Clinical Research Support Services Division)

Adhiambo Opondo-Asiyo

Health Information Advocate and Acting CEO

Adhiambo Opondo is a passionate advocate who transforms personal commitment into practical action, empowering communities through education, counseling, and advocacy for people living with sickle cell disease.
As Founder of the Birthmark Foundation, she creates awareness of birth injury, birth trauma, and genetics.
Currently running a campaign, “Adopt a warrior,” to help purchase hydroxyurea for vulnerable children living with sickle Cell Disease.
She has authored children’s literature on sickle cell disease,” Little Brave Cells”. She is developing resources to support young people transitioning into adolescence and adulthood while living with the condition.

Evans Odipo

Regulatory Specialist

Evans Odipo is a trained clinician by profession holding a Diploma in Clinical Medicine and surgery with a Bachelor’s degree in Public Health. He is currently a Regulatory Affairs Specialist and has over 20 years experience in different disciplines of clinical research including clinical monitoring, quality assurance, and regulatory compliance across multiple therapeutic areas of communicable diseases like HIV/AIDS, TB, Malaria and COVID-19

Dr. Momanyi Ogeto

Dr. Momanyi Ogeto

Clinical Research Support Services Lead (CRSS Division), Acting Director

A clinical research professional leading Clinical Research Support Services (CRSS) activities, overseeing the coordination and delivery of clinical trial support functions, and serving in an acting director capacity to ensure alignment with established protocols, applicable guidelines such as International Council for Harmonisation Good Clinical Practice (ICH-GCP), and organizational objectives

Susan Musau

Laboratory, Quality and Accreditation Lead

Susan Musau is currently a PhD student in the Department of Medical Microbiology and Immunology at the University of Nairobi, where her research focuses on the diversity and phylogeny of Mycobacterium tuberculosis complex (MTBC) strains in Kenya using whole genome sequencing. She previously served as the Laboratory Technical Advisor for the Kenya Population-based HIV Impact Assessment (KENPHIA) at CIHEB Kenya until September 2025 and also worked as a Regional Laboratory Advisor with University of Maryland Programs. She specializes in the implementation of Quality Management Systems (QMS) and has supported numerous laboratories across Africa toward accreditation based on ISO 15189 standards. Previously, she worked with the Kenya Medical Research Institute in collaboration with the Centers for Disease Control and Prevention (KEMRI/CDC) as the TB Laboratory Deputy Director and Laboratory Quality Assurance Head. During this period, she gained extensive experience in tuberculosis diagnostics and research, including sample reception and processing, microscopy, GeneXpert testing, mycobacterial culture, line probe assays (LPA), drug susceptibility testing (DST), immunological assays, and sequencing. She has participated in cohort studies, operational research, and clinical trials, including the Aeras vaccine trials, Tuberculosis Trials Consortium (TBTC), and AIDS Clinical Trials Group (ACTG) studies. Susan holds a Master of Health Science degree from the University of Maryland Baltimore, a Master of Arts in Project Planning and Management from the University of Nairobi, a Bachelor of Science in Medical Laboratory Science, and a Diploma in Medical Laboratory Technology. She is registered and licensed by the Kenya Medical Laboratory Technicians and Technologists Board (KMLTTB).

Nondi Akombo Moses

Senior Clinical Research Associate

Nondi Akombo Moses is a highly experienced Clinical Research professional with over 9 years of progressive expertise in oncology, hematology, infectious diseases, and multi-site clinical trial operations across East and West Africa. He holds a Diploma in Clinical Medicine and Surgery and a Bachelor of Science in Clinical Medicine, Surgery and Community Health, with additional professional training in clinical trial operations, project management, and leadership in health. He has extensive experience supporting Phase I–IV clinical trials, feasibility studies, cohort studies, and multi-arm multi-stage (MAMS) trials in compliance with ICH-GCP, IRB, and regulatory requirements. He has led site initiation, monitoring, regulatory coordination, SAE oversight, quality management, source data verification, and sponsor-facing study operations across multiple research sites. He is skilled in TMF/eTMF management, EDC systems, protocol compliance, audit readiness, pharmacovigilance, and site feasibility, with a strong track record of strengthening research systems, mentoring site teams, and ensuring high-quality clinical trial delivery in resource-limited settings.

Judith Adhiambo Owino

Statistician

Judith Adhiambo Owino is a Statistician and data professional based in Nairobi, Kenya, with a BSc in Applied Statistics with IT from Masinde Muliro University of Science and Technology. She has experience across clinical, public health Education, Agriculture and large-scale survey research, including a pediatric health intervention study in Homa Bay, a World Bank–funded health systems survey, the USAID DREAMS programme, a farmer communication evaluation in Kenya and Tanzania and the 2024 Kenya National School Census. Her expertise covers study design, digital data collection (ODK, KoboCollect, REDCap, CSentry), statistical analysis using R, SAS, SPSS and Stata, and reproducible reporting with R Markdown. She has strong experience in field team supervision, data quality assurance, data analysis and ethical research practices, consistently maintaining high data accuracy and 100% informed-consent compliance.

Andrew Yego

Pharmacology

Andrew Yego is a Molecular Biomedical researcher skilled in proteomics, structural biology, computational modeling, and DNA/RNA analytical workflows, with experience in LC-MS/MS peptide profiling, enzymatic assays, and molecular pathway analysis. Driven to translate molecular insights into therapeutic innovations, drug development, and mechanism-based biomedical solutions through advanced research training

Damaris Juma Okiri

Clinical Research Associate

Damaris Juma Okiri is a highly resourceful, innovative, committed and Creative Clinical Research Professional with 15 years’ experience in clinical trials which included over 5 years Quality Management and Regulatory Affairs and over 4 years Clinical Monitoring of phase I-IV clinical trials. She has an educational background in Nursing, Epidemiology and Biostatistics. She possesses an in-depth knowledge and experience in ICH-GCP guidelines, Safety reporting, Site Management, Recruitment and Screening, GCP auditing, Vendor Qualifications, IP accountability and Reconciliation. She has a strong experience in setting up, implementing, and managing quality systems in clinical trials to support delivery of ethical studies and quality data.

Felix O. Adundo

Clinical Research Associate

Felix O. Adundo is a Senior Clinical Research Associate with 6+ years of progressive experience in clinical trial monitoring, study start-up, regulatory submissions, and multi-site project oversight across oncology, infectious disease, and HIV/AIDS trials. Experienced in full-cycle monitoring (selection through close-out), protocol and CRF review, ICF development, and risk-based monitoring strategies. Demonstrated leadership in site management, training of junior staff, and ensuring inspection-ready compliance with ICH-GCP, FDA, and local regulatory requirements. Proven ability to independently manage multiple projects while maintaining quality, timelines, and budget adherence.

Charles Kato

Charles Kato

Community Healthcare Lead

A clinical research professional supporting and coordinating clinical trial activities in Uganda, ensuring studies are conducted in line with established protocols, International Council for Harmonisation Good Clinical Practice (ICH-GCP), and relevant local regulatory requirements, while serving as the in-country representative for clinical research-related coordination

Dr. Busolo Nicholas

Business Development Lead (Commercial Division)

Dr.Busolo is a Senior Business and Management Lecturer at Management University of Africa and Managing Director Nuru Ya Masomo Link Consultancy ‘Transforming Lives through Education’

Victor Omondi

Victor Omondi

Health Systems Strengthening Lead

This is Victor Omondi, Health Systems Strengthening Lead, with over 7 years of experience in biomedical research, forensic science, and medical biochemistry

Brenda Misiko

Senior Clinical Research Associate (CRSS Division)

Senior Clinical Research Professional with 10+ years of progressive experience
from Registered Clinical Officer, Study Clinician, Regulatory Affairs, Internal
Monitor and Study Coordinator to Clinical Research Associate II. Proven
success in project management, planning and tracking of study progress, site
feasibility, site selection, onsite/remote monitoring, drafting clinical and
regulatory documents, regulatory submissions, study protocol development,
drafting and negotiation of budgets, management of finance and clinical
operations for 13+ studies. Track record of mentoring junior CRAs, managing
multi-site clinical trials, driving site audit readiness and quality and ensuring
ICH-GCP compliance across Phase I–IV studies, developing and evaluating AI
models. Seeking to leverage strategic, clinical, regulatory, medical writing,
monitoring and clinical research expertise in the Clinical Research
Associate/Clinical Trial Management position.

Have a Question?

Send A Message