Labcorp Drug Development Job - 41294456 | CareerArc
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Company: Labcorp Drug Development
Location: Lisbon, Portugal
Career Level: Mid-Senior Level
Industries: Healthcare, Pharmaceutical, Biotech

Description

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)

NO AGENCIES PLEASE

 

MORE INFORMATION AVAILABLE ON REQUEST

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. 

 

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