Senior Clinical Project Manager - Biotech - United Kingdom
Position: Senior Clinical Project Manager / Program Manager Location: London, however flexible with home based working Reporting Line: VP, Clinical Development Size: Small yet growing! Retained Search Our client is an attractive, stable (yet small), fast-growing organisation based in the UK & US that focus on the development of Urological and Gastroenterology fields. This is an extremely exciting time for the company following a huge investment from various venture capitalist firms, therefore they have the platform to continue to grow across various indications and phases. This is a great opportunity to join a young and exciting company from the get go and have the autonomy to truly impact the organization. This company have a truly talented senior management team with experience across blue chip pharma and small pharmaceutical companies, therefore the selected individual will have regular access to proven pharmaceutical professional enabling you to expand your portfolio! Due to the companies unique stance in the market (huge financial backing, yet small in size), the selected candidate will have the opportunity to make a real difference! (i.e. small team culture and entrepreneurial environment where decisions are made quickly without red tape, while also having the stability/financial backing through there series A funding) Attractive Features: · Huge financial backing = opportunity & stability · Experience yet transparent senior management team · Growth potential - due to several project ongoing, the company is going from strength to strength! · Opportunity to experience further development in Program Management · location & flexibility Position Summary: The Senior Clinical Project Manager (SCPM) will work closely with the VP, Clinical, to manage assigned global clinical studies of varying complexity (Phase 1 - 3). The SCPM is responsible for the management of all sites and vendors (e.g. Clinical Research Organisation, CRO) for each assigned clinical study and resolution of operational issues. Main Responsibilities (please ask for full JD to see extended responsibilities) · Program Management · Clinical Study Management · Vendor Oversight · Budget Responsibilities · Stakeholder Responsibilities · Cooperate Responsibilities Minimum experience requirements: · Clear track record of successful execution of clinical studies from Phase 1 through Phase 3 including: o Detailed understanding of all aspects of clinical protocol design and implementation and overall drug development. o Strong vendor management skills, e.g. CRO, Laboratory and Clinical Supply logistics. o Management of clinical study to budget and timelines. o Ability to write and edit technical documents such as protocols, protocol amendments, informed consent and other study-related documents. · Strong people-management skills and ability to interact and influence successfully at all levels and externally with Board Members, partners and others as necessary. · Knowledge of ICH guidelines, GxP regulations, FDA guidance documents, EU directives. For more information, please reach out to me directly! email@example.com +44 1293 77 66 44 Barrington James is a uniquely successful specialist life science recruitment company and has recently been recognised as a BEST COMPANY To Work For by the Sunday Times. It has enjoyed an exceptional growth trajectory since its launch in 2002, and is now established in the heartlands of the international pharma, medical devices and healthcare industry with consultant staff already approaching 140, and planned to be 180 by the end of 2017. Recruitment companies succeed by matching the specific needs of clients with the true capabilities of candidates. We believe there are 2 reasons for our outstanding performance over the past decade, which benefit our clients and our candidates equally; People & Knowledge Barrington James’ exceptional people and their depth of experience are ready to work for you, now.