Associate Manager, Statistical Programming

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Job description

Job Overview:Associate Manager, Statistical Programming required to work for Labcorp Drug Development in a dual role; both line managing staff and performing a Lead Statistical Programmer roleYou will be employed by Labcorp Drug Development working in our Clinical Pharmacology Services (Phase I Healthy Volunteer studies) department with the opportunity to work across multiple Sponsors and therapeutic areasHome based anywhere in the United KingdomYou must have previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company along with some team supervisory skillsCandidates 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 an Associate Manager, Statistical Programming role. This is a dual role; line managing a team and leading studies. You will work in our Clinical Pharmacology Services group so you will enjoy a varied role working for different sponsors across several therapeutic areas within Phase I healthy volunteer studies. 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 the United Kingdom.Job Primary FunctionsMonitors staff projects quality, timelines and budgets to foresee and correct issues and assure project expectations are met. Help staff identify resource or scope of work changes.Effectively communicate the status of projects to line management and project managersManages discretionary expenses and spending within team in order to meet budgetWork closely with leads to ensure that staff resources are used efficiently, and team is well utilizedManages resources within team: new hires, terminations, transfers, and contractorsCarry out line management responsibilities for assigned staff, including Performance Management and Development activities, disciplinary procedures and administrative activitiesHelps encourage staff career growth and developmentProvides statistical programming support and technical support to team membersAct as the lead programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, ISS and ISE, and electronic submissionsRepresenting Statistical Programming at internal project team meetings, client meetings and auditsContribute to ongoing improvement of programming processes, methodology and documentationFacilitate advanced technical expertise, share knowledge at department meetingsKeeps abreast of new statistical programming practices, methods and tools, regulatory practices, and industry trends to stimulate departmental growthEducation/Qualifications:Bachelor's degree, preferably in mathematics, statistics, computing, life science, health science, or related subjectsExperience: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 skillsExtensive experience and proven skills in the use of SAS® programs within a clinical trials environment including all processes/practices used with a Statistical Programming environmentKnowledge 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 ManagementStrong supervisory skills, and ability to organize their own and others' workGood problem solving skills, and a willingness to take ownership of decision-makingInterpersonal and effective communication skills; able to communicate appropriately internally and with clients.Knowledge of the metrics, tools and processes used to manage projectsDemonstrates basic knowledge of clinical research guidance, including FDA, international regulatory agencies, ICH, and GCPCandidates must be fluent in English language (both verbal and written) NO AGENCIES PLEASEMORE INFORMATION AVAILABLE ON REQUESTFor a confidential discussion about this opportunity, please phone Peter Lewis on (0) . 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