Educated in Business Studies and Marketing, Rob has spent over 25 years’ profitably building multinational and early stage businesses within Pharmaceutical, Medical Devices, Diagnostic and Consumer Healthcare market sector and in 2004 he founded Roboleo & Co with a specific focus on innovation, market entry and customer engagement. Read More »
Rob started his career in marketing research at Boots before moving into marketing and general management positions with RPR, Pharmacia, Unipath (Unilever) and Bayer. In addition, he has held executive and non-executive directorships of SMEs within the pharmaceutical and healthcare industry.
As a strategist Rob brings a detailed understanding of how devise innovative, differentiated and compelling market entry strategies. However, he passionately believes that success (or failure) is primarily driven by how well strategies are implemented and ensures that these principles are integrated into every assignment.
Iain is an experienced Medical Communications professional with extensive experience gained over the last two decades. Prior to this, he spent the early part of his career in the Pharmaceutical industry in a variety of commercial roles including senior sales and marketing positions. Iain has also worked in Diagnostic markets in both the UK and internationally. Read More »
His Med Comms experience spans both big pharma, having managed projects for many leading pharmaceutical companies as well as many pharma/biotech SME’s. More recent experience has involved working on ATMP’s for rare disease, including Stem Cell and Gene Therapies.
Iain has worked with senior payers, clinicians, patient groups and institutions throughout Europe and the US over a number of years and has a deep understanding of the many key issues facing the pharmaceutical healthcare industry in today's ever-changing landscape. He is a highly experienced communications project manager and has extensive experience working with and managing cross functional teams.
Chris is Chair in Health Economics (specialising in HTA) at the University of Leeds. He is an empirical health economist specialising in the analysis of observational datasets and their role in HTA. He combines a technical expertise with an ability to understand the bigger picture, specifically where and how new technologies can demonstrate their economic argument, early identification of the challenges of demonstrating that argument and knowing which elements of an argument to enhance and those which should be avoided within an economic evaluation framework. Read More »
Previous positions include Senior Research Fellow at the Centre of Health Economics (CHE) at the University of York and a director of a leading international health economic consultancy.
He joined Roboleo & Co in 2009.
Laura has a BA in Business Economics, an MSc in health economics and a PhD in Economics from the University of York. Her PhD looked at structural uncertainty within decision analytic models and the use of expert elicitation. She joined the economic evaluation team at the Centre for Health Economics (CHE), University of York, in 1999. Read More »
Laura has worked on a wide range of applied and methodological projects and has gained extensive experience of modelling the cost-effectiveness of arthritis and musculoskeletal diseases, especially psoriatic arthritis. Her research interests include:
Laura has been working with Roboleo & Co since 2011, bringing her considerable experience in technology assessment, both trial-based and modelling projects to clients. She has worked in a wide range of disease areas and has contributed towards assessments undertaken for the technology appraisals process at NICE.
In addition to her work at Roboleo Louise has over eight years’ experience as an academic researcher at the University of Exeter Medical School specialising in health technology assessment and health economics, as well as experience of using evidence synthesis and budget impact modelling in local decision making in a clinical commissioning group (CCG). Read More »
The majority of my academic experience has been as a health technology assessment analyst for the Peninsula Technology Assessment Group (PenTAG), one of 10 teams conducting research to support the work of the UK National Institute for Health and Care Excellence (NICE) HTA programme. This included systematic reviews of diagnostic test accuracy, systematic reviews of clinical and cost effectiveness, and the critique and development of de novo health economic models.
In addition, she has experience of using evidence synthesis in the local decision-making process through her role as Clinical Evidence Scientist at the North East and West (NEW) Devon CCG, conducting rapid reviews of both interventions (without NICE guidance), surgical procedures to summarise available clinical and cost-effectiveness evidence as well as conducting budget impact analyses.
Louise’s consultancy experience includes:
Louise holds an MSc in Health Economics and Health Policy from the University of Birmingham (2014), and a BA in English Language and Literature from the University of Swansea.
Vanessa is a Senior Medical Writer with over 20 years of experience in the pharmaceutical industry. She has an MPhil/PhD from Cambridge in Cardiovascular Pathology (1993) and held a Postdoctoral research position in the Oncology Department at Cornell Medical School, New York (1993-1995). Read More »
In subsequent positions as Editorial Director, Head of Medical Writing and Director at leading international medical communication companies in the US and UK, she has been involved in the production of a wide range of global and regional medical education materials. These have included peer-reviewed publications; meeting, marketing and training materials, systematic literature reviews; as well as information for patients. In recent years, she has had particular experience in producing a variety of digital material, including content for web platforms, animations, e-learning materials and easy access tools to help support and improve clinical decision-making. In addition, she has aided in the preparation of submissions for SMC and NICE.
She has extensive experience working across a wide range of therapeutic areas and has worked directly with many worldwide key opinion leaders.
Mark is a medically-qualified and highly experienced drug developer with 20 years' pharmaceutical R&D experience. He has worked at all phases of clinical drug development across a wide variety of therapeutic areas, including orphan diseases. He was a Global Clinical R&D Director and then Director of Science and Medical Public Affairs at Pfizer in Sandwich. Earlier in his career he was an NHS anaesthetist and intensive care doctor. Read More »
He has also significant experience at the R&D interfaces between academia, the NHS and the biopharmaceutical industry e.g. having helped lead the establishment of the MRC/industry pre-competitive consortia in COPD and RA and the UK Government's Translational Research Partnership Programme.
Mark has been a Medical Advisor to Roboleo & Co since 2011 and provides 'hands-on' clinical, scientific and policy leadership to small and medium-sized pharmaceutical companies. He is currently Director of the South West Academic Health Science Network.