At ClinFlex Partners, our people are at the heart of everything we do.
We collaborate with a global network of seasoned life sciences professionals who bring deep expertise, operational excellence, and a shared commitment to delivering results that matter.
From clinical development leaders and regulatory strategists to safety experts, medical writers, and program managers—our people have been there, done it, and know how to get it done.
They don’t just consult—they embed, lead, and deliver as trusted extensions of your team.
Whether you're launching a first-in-human trial or preparing for global commercialisation, our professionals integrate seamlessly into your team, ensuring speed, continuity, and precision from day one.
Brian is an accomplished leader in global project management for clinical Development and Process Improvement with over thirty five years of experience within global pharma and ‘top 5’ CRO’s.
With a background in analytical biochemistry and a Lean Six Sigma Black Belt he has strong analytical and leadership skills combined with a broad experience of monitoring, project and line management across all key clinical services. Additionally he has focussed on measuring and improving key operational metrics and process improvement to define and achieve strategic goals for a number of CRO and pharma clients.
Clinical research professional with over 16 years of progressive experience in leading and managing global clinical trials in phase I, II, II and IV. Experience of leading and managing cross functional, cross cultural global teams. Liaise and maintain professional and scientifically aligned relationship with internal and external stakeholders e.g. KOL’s. Experienced in various therapeutic areas such as ophthalmology, Immuno- Oncology and Hepato-oncology, CNS - Psychiatry, Epilepsy and Major Depressive Disorder, Infectious diseases – Influenza vaccine, Paediatric vaccine, HIV and COVID-19 clinical trials. Experienced in setting up clinical trials in USA, EMEA, APAC, Middle East, Russia, Ukraine and Africa region.
13+ years of regulatory affairs experience in supporting European and Global markets, having worked for both Pharma companies and CROs / consultancy companies. Successfully supported a number of projects in various therapeutic areas such as virology, cardiovascular, metabolic, neuroscience and oncology. Helped launch a service in the UK and US for a health care provider start-up based in the USA. Supported data compliance activities and overall marketing and adverting activities. Project managed large scale regulatory affairs projects. Master in Pharmaceuticals Sciences, with a post-graduation in Integrated Management Systems (ISO 9001; ISO14001; OHSAS 18001) and Certification in Management Consulting and Project management (PRINCE 2 certification). Fluent in both English and Spanish.
15 years of experience working for Pharma / Biotech companies and Clinical Research Organizations (CROs). Worked in various roles encompassing Pharmacovigilance, Medical Information, Clinical Trials and Clinical Data Management. Good understanding of FDA guidelines, Good Clinical Practice (GCP), International Conference of Harmonization (ICH) and local regulatory guidelines. Experience in various therapeutic areas including oncology, rare diseases, vaccines, nutritional supplements, CVRM and Respiratory. Lead GVP Audits independently and contributed in QMS Audit and Health Authorities inspections (GMP/GDP and GCP).
Pro-active and multitasking Clinical Research Associate (CRA), with 10 years’ experience. Educated in clinical research and business; experienced in Monitoring Phase I trials as the project lead. Phase II- III as part of multi-country programs. Ricardo has excellent communications skills. A good leader, good change manager, and team players is Proactive and results oriented. Spanish and English proficiency.
An experienced field based clinical professional (CRA/CTM/site liaison), with over 25 years’ experience in both IMPs and medical devices. Experience of all phases and aspects of the trial process, including UK IRAS/EC/HRA/CRN submissions and site set up. Interpersonal and site management skills of the highest standard, effective time management, organisational and IT/technology skills, enable autonomous working and proven results. I specialise in taking on challenging sites and working with them to resolve their issues and get them back on track.
Executive quality leader with over 20 years extensive experience in strategic direction and oversight of global teams in cGMP environments. Proven track record in regulatory compliance and commercial manufacturing of oral dosage drugs, biologics, cell, tissue therapies and medical devices. Expertise in global quality assurance, regulatory affairs and quality control fostering high-performing operational teams in pharma and medical device sectors. During my tenure I have submitted over a dozen IND's, three BLAs and EU IMPD and successfully accomplished pre-approval inspections for several clients.
Pharmalancers, our proprietary global platform has over 350 vetted experts across every major function in drug development and in key geographies.
This gives us the ability to match the right person to the right project—at exactly the right time—offering our clients unmatched agility and confidence.
Pre-vetted, senior-level talent
Rapid deployment and onboarding
Global reach with local insight
Embedded team members with accountability
Fractional, flexible, and full-service models
Cost-Effective – You only pay for the expertise you need, when you need it—no unnecessary overhead
