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Sunday 5 May 2013

Clinical Project Manager (CPM) - Late Phase - Home or Office Based


Job Description

I have an exceptional role for an experienced Clinical Project Manager. I am looking for a home or office based CPM in UK to work on Late Phase clinical trials (peri and post approval). Reporting into the European Head of Project Management. My client is a growing CRO who specialise in global clinical trials for the pharmaceutical industry. Due to some exceptional years of success, the team are growing extensively in Europe. They are looking for an experienced and established Clinical Project Manager with a solid backgroun in Late Phase trials to hit the ground running. On offer will be the opportunity to work on projects across separate therapeutics areas.

Requirements:
  • Experienced at working closely with clients, you will ensure that studies are fully conducted in accordance with timelines, budgets as per agreed contracts. Combined with company SOP’s.
  • Primary liaison with Customers, vendors, and Investigator Sites.
  • An integral part of the business development team through involvement in proposal development and bid defence.
  • Financial reporting and control, therefore managing profit-margins,
  • The individual will be responsible for phase IIIa, IIIb, IV post marketing studies, therefore would ideally suit someone who has had exposure to post marketing project management previously as well have having worked on UK and / or European projects.

Desired Skills & Experience

Qualifications
  • Minimum Bsc in the life sciences, nursing degree, or equivalent combination of education and experience.
  • Proven clinical research experience in a contract research organisation (CRO), pharmaceutical, or Biotechnology Company.
  • Previous technical and managerial experience in conducting multi-national and/or local clinical trials in a hospital setting, pharmaceutical company, or CRO preferred.
  • Thorough knowledge of regulatory requirements, drug development, and clinical monitoring procedures.
  • Demonstrated proficiency with ICH/GCP guidelines.
  • Proficient computer skills in Word, Excel, PowerPoint, email and Internet.
  • Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
  • Good communication and interpersonal skills.
  • Strong written and spoken English.

To apply
Please send your CV to greg.bell@morganprestwich.com or call me on +44 1737 22 66 44
Keywords: clinical project manager, clinical project management, study manager, clinical trials, clinical trial manager, CTM, senior clinical research associate, lead clinical research associate, Lead CRA, LCRA, SCRA, senior CRA, clinical data manager, clinical safety, clinical research, project manager, CPM, Phase I, Early Phase, Pre-clinical, Phase I and II, Phase I & II, Phase I – IV, Oncology, Neurology, Infectious Diseases, Rheumatology, psychiatry, CNS, Central Nervous System, Women’s Health, haematology, GI, Gastroenterology, Vaccines, Ophthalmology, Orthopaedics, Urology, UK, South, South East, London, Home Counties, CRO, Pharmaceutical, Medical Device, Biopharmaceutical, surrey, sussex, hampshire, berkshire, hertfordshire, essex, kent, London, France, Europe, Germany, Belgium, Netherlands, Spain, Portugal, Switzerland, Italy, Austria, Luxembourg, Late Phase, Phase III - IV, Phase IV, Business Development, Sales, CRO, USA, America, United States of America, US, East Coast, Central, Southern, West Coast, Clinical Research, Registries, Clinical, Medical, Pharmaceutical, Europe, Business development, BD, senior, director, germany, switzerland, Austria, European, europe, sales, CRO, Contract research, clinical research, phase, late phase, Phase IV, Phase I - IV, full service, registries, post marketing, Keywords: Late Phase, Phase III - IV, Phase IV, Business Development, Sales, CRO, Germany, France, UK, The Netherlands, Belgium, Spain, Austria, Switzerland, Clinical Research, Registries, Clinical, Medical, Pharmaceutical, Europe, contract research organisation, CRO, clinical trials, clinical research, CRA, CPM, SCRA, BD, RFI, RFP, new business development, clinical sales, bid defence, DBD, BDM, Director business development, early phase, later phase, Phase IIIb, phase IV, registries, Cohorts, Case-control  studies, Pragmatic trials, Lifecycle Decision Analytics, HTA Strategies & Regulatory Approvals, Advanced Modelling & Health Economics, Market Access & Pricing, Real World Impact Database Studies, Risk & Benefit/Risk Management, Observational studies, Observational relative effectiveness studies, Coverage with evidence development (CED), Post-Authorization Efficacy/effectiveness study (EMA’s PAES &FDA PMCs), EU HTA dossiers &  US Payers interestWe specialise in advanced designs for the study of relative effectiveness, Disease cohorts with dynamic exposure, Mirror image studies, Case-cohort studies, Systematic case-referent studies, Historic-Prospective designs, Pragmatic trials (support), Assessment of the Burden of Disease, Usual care, standard of care and comparators studies, Niche identification and position, BoD assessment in cost-effectiveness studies, HTA dossiers, Pricing & Reimbursement, Payer Research, Cost-consequence analysis, Cost calculators, Cost-effectiveness analysis, Cost-utility analysis, Budget impact analysis, Market & Revenue Forecast

Company Description

Morgan Prestwich Recruitment Limited is a fully integrated Pharmaceutical Recruitment Consultancy, providing tailored services to our Clients & Candidates needs within all levels of the Pharmaceutical, Biotechnology, Medical Devices and Clinical Research industries. We operate globally, attracting international clients and candidates throughout the industry.

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