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Team 2018-05-29T09:59:21+00:00

Jaswinder Khera – Managing Director US

At WEP Clinical, Jaswinder oversees the growth and strategy of the business in the Americas. Jaswinder brings over 30 years of experience in the Pharmaceutical Industry in senior sales and marketing positions with Sanofi, MSD and Astra. He also held senior management positions in operations and business development during his 10 years with Quintiles.

Jaswant Khera – Managing Director EU

Following sales and management experience with Pfizer, where he led a team that marketed the global blockbusters Lipitor & Neurontin, Jaswant went on to launch WE Pharma, now called WEP Clinical. He brings with him 20 years of commercial, strategic, operational and marketing experience as well as a deep understanding of international markets and commercialization of drugs. Currently serving as Managing Director EU, he is responsible for the growth and strategy of the business.

Matt Comstock – Vice President, Business Development

Matt has nearly two decades of experience working in the Pharmaceutical and CRO space. He worked previously in data management and finance at Quintiles for nearly 15 years, and also has experience in research, strategic account management, sales and relationship development. As the Business Development Director at WEP Clinical, Matt is responsible for developing new customer accounts as well as growing relationships with existing customers.

Amandip Sidhu – Expanded Access Programs Director

Amandip has harnessed a clinical background in pharmacy to develop industry-leading solutions. Previously, as part of an international PLC healthcare company, he was responsible for creating and implementing the company’s EAP strategy. Now at WEP Clinical, Amandip is responsible for overseeing all expanded access activities and ensuring WEP’s programs are run efficiently and to the highest standard of quality. 

Carlos Marafusta – Business Development Director

Carlos joined WEP Clinical in 2013 and is currently the Business Development Director in the EU. He has an in-depth knowledge of the unlicensed specialty care market and over 20 years experience in the industry across a range of disciplines, including commercial, strategic, operational and sales and marketing roles for companies such as Bristol Myers Squibb and Astra Zeneca.

Megan Batchelor – Operations & Quality Director

Megan has been in the pharmaceutical industry for over ten years and has extensive experience in facility startup, quality operations, engineering, and project management. She joined WEP Clinical in 2016, after working at Novartis Vaccines & Diagnostics, and currently serves as the company’s Operations & Quality Director. In her role, Megan is responsible for helping to grow and develop quality systems and processes while focusing on continuous improvement of current operational processes.

Entrane Harvey – Director of Project Management

Entrane has been in the Pharmaceutical and CRO industry for over twenty-seven years with extensive experience in Global Project Management and Clinical Operations. He joined WEP Clinical in 2017 after working at Glaxo SmithKline. In his new role, Entrane is responsible for overseeing all expanded access project management activities as well as ensuring the growth and the development of solid project management systems and processes for EAP Programs that drives value and superior quality for our clients.

Sean Quigley – Operations Manager

Sean Quigley manages the warehouse and logistical operations of WEP EU and brings with him 25 years of experience in supply chain management. Having previously worked for AAH he has managed end-to-end logistics operations, covering the full range of medicines including Controlled Drugs and Temperature sensitive product,  as well as overseeing stock management. He supports the sales teams to develop bespoke logistics solutions for WEP’s customers.

Richard Crawley – Regulatory Affairs 

Richard has over forty years’ experience in the pharmaceutical industry in preclinical drug metabolism and pharmacokinetics, global regulatory affairs and drug development planning and management. He has served in senior regulatory positions with the Welcome Foundation (UK), Burroughs Welcome (USA) and Pozen Inc. (USA), covering Phase I – IV development activities, and he has extensive experience interacting with worldwide regulatory authorities.

Chris Barnett – Regulatory Affairs 

Experience in the principles of International Quality Assurance and project and line management gained in various tenures at the Wellcome Foundation Limited, Glaxo Wellcome and Glaxo SmithKline, led Chris to his certification as an EU Qualified Person (QP) with particular expertise in clinical trial materials. His forty years of experience enables him to provide expert knowledge of the principles and regulation of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and Quality Assurance.