Manager, Statistical Programming
Labcorp Drug Development
Lisbon, Portugal
há 3 dias

Job Overview :

  • Manager, Statistical Programming required to work for Labcorp Drug Development in a dual role; both line managing staff and performing a Lead Statistical Programmer role
  • You will be employed by Labcorp Drug Development working in our Clinical Development Services (PII-IV) group with the opportunity to work across multiple Sponsors and therapeutic areas
  • Home based anywhere in Europe or office based in any of our European offices
  • You must have previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company along with some team supervisory skills.
  • Candidates must be fluent in English language (both verbal and written)
  • Join our growing team and discover your extraordinary potential by working for Labcorp Drug Development in a Manager, Statistical Programming role.

    This is a dual role; line managing a small team and leading studies. You will work in our Clinical Development Services group so you will enjoy a varied role working for different sponsors across several therapeutic areas within phases II-IV.

    The position offers a strong support network, flexible working solutions and the opportunity to progress your career. If you are looking to strengthen your supervisory and Lead expertise within a varied and dynamic environment, then this is a fantastic opportunity.

    This is a permanent, full-time office or home-based role anywhere within Europe.

    Job Primary Functions

  • Participates in proposal development for standalone, small programs and / or new drug applications (NDAs) and in bid defense.
  • Actively monitors staff projects quality, timelines and budgets to foresee and correct issues and assure project expectations are met.
  • Manages discretionary expenses and spending within team in order to meet budget
  • Work closely with leads to ensure that staff resources are used efficiently, and team is well utilized
  • Manages resources within team : new hires, terminations, transfers, and contractors
  • Carry out line management responsibilities for assigned staff, including Performance Management and Development activities, disciplinary procedures and administrative activities.
  • Helps encourage staff career growth and development
  • Provides statistical programming support and technical support to team members
  • Act as the lead programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, ISS and ISE, and electronic submissions.
  • Participates in internal and client audits, and regulatory inspections.
  • Contribution to review and amendment of departmental processes and supporting documentation.
  • Facilitate advanced technical expertise, share knowledge at department meetings
  • Keeps abreast of new statistical programming practices, methods and tools, regulatory practices, and industry trends to stimulate departmental growth
  • Education / Qualifications :

  • BSc, preferably in computing, life science, mathematical or statistical subject
  • Experience :

  • You must have previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company along with some team supervisory skills.
  • Extensive experience and proven skills in the use of SAS® programs within a clinical trials environment including all processes / practices used with a Statistical Programming environment.
  • Knowledge in all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.
  • g. Biostatistics and Clinical Data Management.

  • Strong supervisory skills, and ability to organize their own and others' work.
  • Strong problem solving skills, and a willingness to take ownership of decision-making.
  • Interpersonal and effective communication skills; able to communicate appropriately throughout Covance and with its clients.
  • Good knowledge of the metrics, tools and processes used within Covance to manage projects.
  • Demonstrates knowledge of clinical research guidance, including Food and Drug Administration (FDA), international regulatory agencies, international conference on harmonization (ICH), and good clinical practice (GCP).
  • Candidates must be fluent in English language (both verbal and written)


    For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 1628 543 457. To apply, please click on the APPLY button.

    Keywords :

    Labcorp Drug Development, Covance by Labcorp, Lead Statistical Programmer, Senior Statistical Programmer, Covance, Statistical programming, Chiltern, Covance, Phases I-IV, Programmer Analyst, Stats Programmer, Senior, Statistical Programmer, Lead SAS Programmer, Manager, line manager, line management, supervisor, CDISC, ADaM, SDTM, Biostatistics, Senior Statistician, Biostatistician, Statistics, Study Biostatistician, pharma, pharmaceutical, SAS, STAT, home based, pharma, pharmaceutical, home-based, flexible working, flexible location, home based, field based, home based EU Anywhere, anywhere in Europe, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia, Madrid, Barcelona, Spain, Ukraine, oncology, cancer, #LI-PL1, #LI-Remote, Remote, EMEA

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