Paul Rice Email & Phone Number

Greater Brighton And Hove Area

- Create synergies where product and process meet- Lead Global Project Management (GPM) operational readiness for all facets of the product, overseeing training and support for cross-functional areas aligned to GPM- Provide matrix leadership support and motivate geographically dispersed GPM teams- Execute financially-sound resource management solutions, allowing teams to scale in response to changing needs based on a comprehensive set of metrics- Partner strongly with the Commercial teams to ensure client expectations are met and to realize continued portfolio growth with subsequent gain of market share- Work closely with Product to ensure the voice of the customer is heard and the Product roadmap is prioritized effectively- Drive department initiatives from identification through to implementation

United Kingdom

- Responsible for the Project Management function outside of the USA (covering EU and APAC)- Primary point of escalation for any issues encountered for non-USA accounts- Support Commercial needs and attend Bid Defences, Capability Meetings and relevant conferences - Coordinate employee development plans and annual performance appraisals- Make salary, bonus, and promotion recommendations, resolving performance/behavioural issues as necessary- Account Management of clients ensuring that projects are delivered in accordance with client specific procedures within Signant Health processes

Reading, United Kingdom

Refer to Senior Director Project Management role above

Hove, East Sussex Uk

- Creating and managing the clinical program strategy- Responsibility for program level forecasting and budget- Overall management of clinical trials; including site selection, vendor and CRO selection and subsequent oversight- Oversight of protocol development- Oversight of data collection and synthesis- Supervising the preparation of technical and scientific publications- Liaising with KOLs and assisting with the preparation of symposia

London, United Kingdom

- Responsible for the Project Management function across the UK- Primary point of escalation for any issues encountered for EU accounts- Support Business Development needs and attend Bid Defences, Capability Meetings and relevant conferences - Coordinate employee development plans and annual performance appraisals- Make salary, bonus, and promotion recommendations, resolving performance/behavioural issues as necessary- Account Management of clients ensuring that projects are delivered in accordance with client specific procedures within Bracket processesNOTE- Started as a Project Manager in March 2009 before getting promoted to lead the Project Management Office in November 2009 as Manager, PMO. - Subsequently promoted again in December 2010 to a Programme Manager position and this title was later realigned to an Associate Director position in January 2012

London, United Kingdom

- Central point of contact for Takeda affiliates regarding review and approval processes- Generation of SOPs, including: Review, approval and conduct of Investigator Initiated Trials (IITs), Medical Information Enquiries, signing off promotional materials and relationships with health professionals- Responsible for training on Medical & Scientific Affairs SOPs and facilitating training across Takeda- Managing IITs including budget reporting and liaison with Investigators and Coordinators- Facilitating review of all trials, publications and Investigator Sponsored Research (ISR) from Takeda affiliates- Ordering clinical supplies and liaising with drug packaging CROs including sign off in accordance with Annex XIII

London, United Kingdom

- Responsibility for all issues relating to the UK office - Attending and coordinating sales meetings for European clients- Attending speculative partnership meetings with other CROs- Identifying appropriate processes and procedures for the UK office, including communication structure and how to effectively manage trials from the UK - Project Manage (including training, study support and client liaison) European trials

Crawley, West Sussex Uk

- Overall responsibility for ECG services for a range of sponsors/CROs across Phase I through to Phase III trials- Working closely with sponsors and internally the Study Implementation team and medical adviser to ensure appropriate design of the clinical trial process- Training of investigators in study procedures, both on site and during global investigator meetings - Maintenance of appropriate communication with the centralised ECG laboratory in the USA NB Started as a Business Development Specialist in Oct-04 before being promoted in Mar-05

Reading, United Kingdom

- Line management responsibility for a team of researchers of various levels and ability- Conducting reviews with current staff and interviews with prospective employees- Ensuring that all studies under my control are performed in accordance with GCP and internal SOPs- Achieving project goals of data management and turnaround within budget and timelines- Managing individual studies on an day-to-day basis with effective client communication in the absence of my staff- Undertaking research in Phase I units, training and testing volunteers on the CDR system- Attending Investigator Meetings or sites to train personnel on the CDR product- Attending seminars and conferences to promote the companyNB - Started as a Research Associate in Jul-02 before being promoted to lead a team in May-03

Master Of Business Administration (Mba), Distinction

In addition to gaining a Distinction I was also awarded the Dean's Prize for the Most Outstanding Student on the Master of Business.

Ba (Hons), Psychology With Management, 2:1