CROMSOURCE has been a trusted partner for European clients conducting work in the United States and Canada for nearly 15 years. During that time our focus has been to build an expert and flexible infrastructure in North America providing comprehensive clinical research services to clients in Europe. From the provision of Regulatory Strategy consultancy and FDA/Health Canada representation to operational delivery of complex, multi-site projects involving medicines or medical devices, CROMSOURCE is a trusted partner. Our European clients benefit from our experience in the US and Canada, and appreciate that when their development plans include North America, the CROMSOURCE team will be there at every step, delivering expert regional support but from a European perspective.
As a partner with a wide range of experience our clients rely on CROMSOURCE to flexibly and proactively support them with services carefully tailored to their needs. Whether this is the inclusion of a small number of North American sites in a multinational project, or the delivery of a large multi-trial clinical development programme entirely in North America, CROMSOURCE has the experience to offer immediate benefits to our European clients. Our work for European clients in the US and Canada has supported successful marketing applications with the FDA, and ranges from complex early phase studies in Oncology, Ophthalmology, and Rare Disease through pivotal studies involving large numbers of sites and patients in Respiratory, Oncology, Orthopaedics, Urology, Audiology, Rare Disease, and Central Nervous System Medicine. Whatever the scope of service or nature of the request, CROMSOURCE keeps our European clients closely informed about the progress of their project in North America with the same ‘one team’ approach which lies at the heart of the CROMSOURCE global philosophy. CROMSOURCE is a safe bridge across the Atlantic Ocean, and represents the ideal partner for European clients including North America in their clinical development plans.
CROMSOURCE North American Executive Team
Chief Commercial Officer and Senior Executive Director, Corporate Development and Strategy
Troy brings more than 25 years of experience in the pharmaceutical and CRO industries, having worked for more than a decade each in increasingly senior positions in specialty pharma and life science services companies. He has a proven track record of success in leading and growing start-up, small, and medium-sized organizations. He has been a managing partner and/or CEO at four companies. Troy holds a PhD in Pharmaceutics from the University of Tennessee and is based in our office in Cary, close to Research Triangle Park in North Carolina.
Vice President, Client Strategy and Development
Kris brings over 34 years of experience in Clinical Development with roles at CROs, Pharmaceutical and Academia. She has worked across all phases of studies in a multitude of therapeutic indications (medicinal and device) and has had increasing responsibilities in many roles in her tenure in clinical research. Kris’s current role is to work closely with clients during the development stages of partnerships while also working with the operational teams within CROMSOURCE to ensure strategy is executed properly while delivering quality output. Kris’ extensive experience in operations ensures that teams are provided key information and resources in order to deliver on all aspects of the clinical trial process.
Director, Regulatory Services
David leads our Regulatory Services team globally, joining CROMSOURCE in 2018 with over 29 years of experience in regulatory affairs within the pharmaceutical and medical device sectors gained in both sponsor and CRO companies. David combines expert knowledge of the regulatory approval system globally with strategic regulatory consulting for our clients and close links to the main divisions with the FDA. David also offers our clients with limited infrastructure in North America the ability to act as FDA representative on their behalf.
Antoinette Torres Frankum
Executive Director, Clinical Research Department
Antoinette has over 25 years of experience in Clinical Development, and joined CROMSOURCE in 2009. In her current role she provides expert executive oversight to all clinical research projects conducted in North America. With Antoinette’s leadership our clients are assured that a highly experienced operational professional is taking care of the delivery of their projects in North America. Prior to joining CROMSOURCE Antoinette held roles of increasing seniority in both CRO and Sponsor company environments and she has a breadth of experience across many therapy areas including medicines, medical devices and combination products. Antoinette is based in our West Coast office near Los Angeles, California.
Global Head, Medical Services Division
Akila is a highly experienced clinical research physician who has worked in the clinical development industry for over 25 years. She joined CROMSOURCE in 2012 and in her current role is responsible for the delivery of exceptional medical services to our clients globally. Akila is a paediatrician by training and holds an MD from the University of Madras and conducted post-doctoral research at Harvard medical school before joining the Industry. Akila is based in our North American Headquarters near Boston, Massachusetts.
CROMSOURCE is an ISO-certified, international contract research organization providing a comprehensive portfolio of services to the pharmaceutical, biotechnology, and medical device industries.
Via Giorgio De Sandre, 3
37135 Verona - Italy
Direct: +39 045 8222811
North American Headquarters:
309 Waverley Oaks Road, Suite 101
Waltham, MA 02452 - USA
Direct: +1 617.871.1128
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