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For more information speak to Mark Cussens on 00 44 1727 817 623

To apply by email markc.26044.5174@keypeople.aplitrak.com

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Senior Clinical Project Manager - Early Phase.Ref: mc 23906

Salary:€575 - €725 per day

Added:08 Jan 2019

Region: Europe

Sector: Pharmaceutical

Sub Sector: Clinical Research

We have an exciting opportunity for an office based contract Senior Clinical Project Management role with a Global blue chip pharmaceutical company. Our client is looking for candidates with early phase clinical trials and also patient study experience. Purpose of the role: Planning and implementation of all operational aspects of assigned Translational Medicine studies (e.g. medium to high complexity studies; first in man, patient studies, multi-center studies, mechanistic studies) from synopsis to reporting according to timelines, budget, operational and quality standards. Responsibilities: Writing clinical protocols and related documents in collaboration with the Clinical trial Team (CTT) Lead the clinical trial protocol development process Lead and matrix manage the global multidisciplinary CTT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures Function as a Lead CTL on studies for Full Development and assist in the coordination of TM related submission documents. Responsible for ordering and management of clinical trial materials Identify sites and manage study set-up Support the CRA on study related questions and serve as point of contact for managing/ answering questions relating to trial procedures and subjects eligibility Responsible for set up and maintenance of the Trial Master File for assigned studies Regularly update all trial information databases in order to manage accuracy of information Approve for all necessary center payments Lead the ongoing review of the clinical trial medical/scientific data (as needed), analysis and interpretation including the development of first interpretable results, clinical trial reports, publications and internal/ external presentations. Co-ordinate pre-audit activities for nominated projects Contribute to identification and evaluation of new centers suitable for performing TM studies in healthy volunteer and patients. BSc or MSc in life sciences or nursing; PhD level scientist with life sciences background; PharmD. Languages: Fluent English (oral and written), knowledge of a second language is desirable. Experience / Professional Requirement: 1. Gained relevant experience (preferred at least 2 years) in Translational medicine, Clinical Research or Research Nurse experience (CRO, academic institution, hospital or industry), as judged from CV/interview 2. Potential to cope with both scientific aspects and operational tasks in a multidisciplinary organization (teamwork). 3. Knowledge of drug development process. 4. Capable of clear written and verbal expression of ideas, an active/proactive communicator. Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment. Please contact Mark Cussens, Clinical Research Recruiter on Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch Key People is a recruitment company with a reputation for providing good value that's been built up over 20 years. -We achieve results faster -Our candidates really are a cut above -We add greater value

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