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Statisticians

Last updated: 11:42 22/02/2013

Senior Biostatistician

Reference number: 2001 Apply for this job Apply for this job »
Type: Permanent, full time Location: West Sussex, office based

Job Description

Summary:

 The role of the Senior Biostatistician is to provide expert statistical input and consultancy to clinical Trials and clinical development projects including design of clinical trials, specification and production of analysis and reporting deliverables (including integrated summaries) on behalf of and/or in conjunction with the company’s clients.

 The Role:

  • Provides statistical consultancy for the design and analysis of clinical projects and/or studies
  • Performs sample size calculation based on clinical input/literature review with regards to expected treatment effects and variability estimates
  • Generates and manages randomisation schedule according to the requirements of the study design
  • Provides statistical input into and reviews clinical protocols and CRFs to ensure that both documents meet the requirements of the study including writing the statistical methodology section of the protocol
  • Provides input to the Data Management Validation Plan (DMVP) to ensure that data are collected and validated to provide high-quality data suitable for statistical analysis and reporting
  • Writes, reviews and manages the Statistical Analysis Plan (SAP) including detailed description of statistical methods planned for the analysis of data and table, listing and figure shells describing the planned statistical outputs. Chair analysis planning meetings with internal and external customers (as appropriate)
  • Reviews (and approves) the clinical database as appropriate for statistical analysis prior to database lock
  • Writes programs to perform inferential statistical analyses according to the requirements of the SAP; performs exploratory analysis as appropriate
  • Provides expert statistical input to Clinical Trials Reports and/or publications; writes the Statistical Methods section and reviews results, discussion and conclusion for appropriate statistical interpretation and inference of results
  • Files and archives all trial statistical documentation
  • Performs quality assurance of deliverables of other Biostatisticians within the department
  • Maintain professional and proactive interactions with internal and external customers
  • Maintain up-to-date knowledge on statistical techniques and procedures
  • Assist in the development of 'best-in-class' analysis and reporting processes
  • Responsible for the specification, programming and statistical reporting of integrated summaries
  • Generate cost estimates for statistical activities in response to client requests
  • Perform budget tracking for assigned trials

Experience/Qualifications required

Skills and Attributes:

 ·         Good organisational skills, plus an understanding of resource and budgeting

·         Good interpersonal and communication skills and the ability to operate effectively in a global working environment

·         Work calmly under pressure and meet deadlines

·         Professional, positive and enthusiastic attitude

·         A good understanding of medical terminology, clinical trial methodology, drug development process and ICH/GCP (especially relating to statistical methodology) 

·         A good investigative and meticulous approach to all activities and tasks

·         Transparent approach, clear and precise

·         Team player

·         The ability to delegate tasks

·         Assist improving the effectiveness of the organisation such as developing new processes, systems and client relations

·         Work effectively and efficiently with internal partners in the company

 Experience:

·         Knowledge/experience in SAS programming (or suitable equivalent data manipulation/statistical analysis software e.g SPSS).

·         Knowledge of global clinical trial practices, procedures, methodologies.

 Qualifications:

 ·         Minimum of a degree (B.Sc.) or equivalent in Medical Statistics or minimum of a degree (or equivalent) in Statistics/Mathematics in conjunction with at least one year’s experience in the application of statistics in clinical trials at a CRO, pharma company or academic institution.

Biostatistician

Reference number: 1992 Apply for this job Apply for this job »
Type: Contract, fixed term Location: Office based in Basel, Switzerland

Job Description

Summary:

 Responsible for all statistical tasks for assigned clinical trials in the Oncology therapeutic area. This includes: protocol writing, analysis planning and reporting, exploratory analyses, publication support, and statistical consultation.

 Reports to Programme Statistician

 Reports to Group Head Biostatistics

 

The Role:

 Coordinate study tasks with other statisticians and statistical programmers.

 Ensure timeliness and adequate quality of all statistical deliverables.

 

  • Follow processes and adhere to the company standards and project standards as well as Health Authority requirements.

Experience/Qualifications required

Skills and Attributes:

 Strong statistical skills and knowledge of clinical trials methodology: experience with protocol development, analysis planning and reporting of clinical trials

 Knowledge of SAS

 Fluent in English, good oral and written communication skills

 Experience in oncology

 Good team player

 High degree of autonomy in performing assigned duties

 Able to establish personal relationships with personnel from other line functions

 Experience:

 At least 5 years experience in pharmaceutical development and clinical research

 Experience with intercultural teams

 

Qualifications:

 Minimum MSc in statistics

Statistician

Reference number: 1991 Apply for this job Apply for this job »
Type: Contract, fixed term Location: Office based in London, UK

Job Description

Summary:

 To work as project/study statistician in multi-functional teams to provide statistical support on clinical trial design, analysis and report.

 Supervisory role in managing external service providers (CROs).

Reporting to Senior Manager of statistics in Data Sciences department.

 The Role:

 1   Works as project/study statistician in multi-functional project teams. Main responsibilities include:

 ·         Provides statistical input in study design, analysis and reporting.

·         Contributes to the development of study synopsis, protocol, (e)CRF design, study report and publications. Co-ordinates and contributes to the development of statistical analysis plan and statistical report. Performs or co-ordinates exploratory analysis as needed.  

  • Represents the statistics function in multifunctional project teams to ensure statistics-related activities conducted by the project teams and CROs are consistent with statistics SOPs, guidelines and standards.

 

2   Participates in the evaluation and selection of external vendors. Provides oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs from the study start-up through archiving. Reviews and validates statistics related CRO deliverables.

 

3   Contributes to the development and implementation of the internal/departmental standards and process improvements.

 

4   Commits to his/her own professional development by attending regular training and conferences, keeping up to date with the latest industry techniques and regulations.

 

5   Provides training to the company employees.

Experience/Qualifications required

Skills and Attributes:

 ·         Good understanding of clinical study designs, statistical inferences and commonly used statistical methodologies.

·         Good knowledge of EMEA/FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.

·         Comprehensive knowledge of the pharmaceutical industry including understanding of clinical drug development process and GCP requirements.

·         Good skill of statistical programming languages including SAS.

 

·         Good project management skills

·         Excellent communication skills and ability to work with cross-functional teams

·         Excellent knowledge of clinical quality standards

 

 

Experience:

 

Ideally 3-5 years of demonstrated experience as a statistician within a Pharmaceutical company, a Biotech or a CRO.

 

 

Qualifications:

 

An Msc or a PhD or equivalent in biostatistics, statistics or mathematics.

 

Statistician

Reference number: 1990 Apply for this job Apply for this job »
Type: Permanent, full time Location: Office based in London, UK

Job Description

Summary:

 To work as project/study statistician in multi-functional teams to provide statistical support on clinical trial design, analysis and report.

 Supervisory role in managing external service providers (CROs).

Reporting to Senior Manager of statistics in Data Sciences department.

 The Role:

 1   Works as project/study statistician in multi-functional project teams. Main responsibilities include:

 ·         Provides statistical input in study design, analysis and reporting.

·         Contributes to the development of study synopsis, protocol, (e)CRF design, study report and publications. Co-ordinates and contributes to the development of statistical analysis plan and statistical report. Performs or co-ordinates exploratory analysis as needed.  

  • Represents the statistics function in multifunctional project teams to ensure statistics-related activities conducted by the project teams and CROs are consistent with statistics SOPs, guidelines and standards.

 2   Participates in the evaluation and selection of external vendors. Provides oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs from the study start-up through archiving. Reviews and validates statistics related CRO deliverables.

 3   Contributes to the development and implementation of the internal/departmental standards and process improvements.

 4   Commits to his/her own professional development by attending regular training and conferences, keeping up to date with the latest industry techniques and regulations.

 5   Provides training to the company employees.

Experience/Qualifications required

Skills and Attributes:

 ·         Good understanding of clinical study designs, statistical inferences and commonly used statistical methodologies.

·         Good knowledge of EMEA/FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.

·         Comprehensive knowledge of the pharmaceutical industry including understanding of clinical drug development process and GCP requirements.

·         Good skill of statistical programming languages including SAS.

 ·         Good project management skills

·         Excellent communication skills and ability to work with cross-functional teams

·         Excellent knowledge of clinical quality standards

 

Experience:

 Ideally 3-5 years of demonstrated experience as a statistician within a Pharmaceutical company, a Biotech or a CRO.

 
 Qualifications:

 An Msc or a PhD or equivalent in biostatistics, statistics or mathematics.

 

 

(Senior) Statistician

Reference number: 1977 Apply for this job Apply for this job »
Type: Contract, fixed term Location: Basel Switzerland

Job Description

Therapeutic Area:   Oncology

 The Role:

 The successful candidate will be responsible for the following duties:

  • Responsible for all statistical tasks on the assigned clinical trials: clinical trial design/planning, analysis plan, reporting activities including exploratory analyses, and additional analysis to support publications.
  • Provide statistical consultation to clinical team and support decision making process by providing adequate information.
  • Track clinical trial/allocated project activities and milestones.
  • Ensure timeliness and adequate quality of all Biostatistics and Statistical Reporting (B&SR) deliverables for the assigned trials.
  • Follow processes and adhere to company and project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, GCP, and regulatory guidelines).
  • Participate in or lead non-clinical project activities as needed.
  • Application and extension of existing Bayesian methods for dose finding and proof of concept
  • Establish and maintain sound working relationships and effective communication within the Clinical Trial Team and B&SR team.

 

Experience/Qualifications required

Skills and Attributes:

 Knowledge and expertise in Statistics, in particular the use of applied Bayesian statistics in decision making.

  • Knowledge of statistical software packages (e.g. WinBUGS, R, SAS)
  • Communicate efficiently with non-statistician colleagues.
  • Able to work with a multidisciplinary team to achieve team’s objective.

 Language Skills:

 Fluent English (oral and written).

 Qualifications:

 Masters Degree in Statistics (or equivalent degree) with at least 2 years of experience or PhD in Statistics (no previous experience is required).

Health Outcomes Statistician

Reference number: 1970 Apply for this job Apply for this job »
Type: Permanent, full time Location: Manchester, UK

Job Description

 The Role:

 Our client is a highly respected International Consultancy in the fields of Health Economics, Market Access and Patient Reported Outcomes which helps its clients bring healthcare products and services to the market successfully by investigating and developing scientific evidence to understand the benefit to patients, clarifying and communicating the value for decision-makers.

 Due to continued growth our client is seeking an experienced statistician with experience in Health Outcomes Research.

 To further develop our client’s analytical and consulting activities in clinical outcomes assessments, we are looking for a senior statistician with a strong background in Outcomes Research, in particular in longitudinal and cross-sectional modelling.

 This is a leadership position in which the successful candidate will advise clients on their outcomes strategy, endpoint development, validation, analysis, and interpretation.

 The Health Outcomes Statistician will also direct project teams for analytical work and lead FDA submissions.

 In return our client offers excellent remuneration, pension contributions, and a sports subscription, together with support for further qualifications, in a friendly and informal

Experience/Qualifications required

Qualifications:

 PhD or Masters degree (or equivalent) in Psychometrics, Biostatistics, Statistics, Epidemiology or Mathematics with significant experience in outcomes research

Biostatistician II

Reference number: 1954 Apply for this job Apply for this job »
Type: Permanent, full time Location: Sheffield or Uxbridge

Job Description

Summary:

 Our client is a top international CRO which is seeking an experienced Biostatistician ideally in its Uxbridge office but our client could also consider its Sheffield office.

 The Biostatistics and Statistical Programming Department is involved in a wide range of therapeutic areas and as part of this group, you will work within a challenging environment, with exposure to many different clients, indications, and compounds.

 The Biostatistician works independently in the programming and quality control of derived datasets and all kinds of statistical outputs (e.g., tables, listings and figures), works under the supervision of an experienced biostatistician in the production of analysis plans and reports, provides basic statistical advice to clients and fulfils the project primary role within a designated project team.

 The Role:

 Key Accountabilities:

 Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques

 Understand and apply moderately advanced statistical methods

 Coordinate and lead a project team to successful completion of a project within given timelines and budget

 Interact with clients as key contact with regard to statistical and contractual issues

 Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents

 Check own work in an ongoing way to ensure first-time quality

 Provide training in statistical analysis to internal clients

 Proactively participate in and/or lead process/quality improvement initiatives

 Mentor and train junior members of the department

 Support of Business Development, e.g. by attending and preparing bid defence meetings

 Travel, attend and actively contribute to all kinds of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results)

 Additional responsibilities as defined by the supervisor/manager.

Experience/Qualifications required

Skills and Attributes:

 - Good analytical skills

 - Good Project Management skills

 - Professional attitude

 - Attention to Detail

 - A good understanding of statistical issues in clinical trials

 - Ability to work independently

 - Good mentoring/ leadership skills

 - Competent in written and oral English.

 Experience:

 - Prior experience with SAS Programming required

 Qualifications:

 - PhD or equivalent in Statistics or related discipline entry level, MSc in Statistics or related discipline with biostatistics experience in a clinical trials environment.

 

Senior Biostatistician

Reference number: 1953 Apply for this job Apply for this job »
Type: Permanent, full time Location: Uxbridge or Sheffield

Job Description

Summary:

 Our client is a top international CRO which is seeking an experienced Senior Biostatistician ideally in its Uxbridge office but our client could also consider its Sheffield office.

 As Senior Biostatistician you will lead the production and quality control of all kinds of statistical deliverables including analysis plans and reports. You will work closely with clients to provide hands-on statistical advice, from study design to discussion of analysis results, whilst fulfilling the project primary role within the project team. You will collaborate with Medical Writing, Data Management, and other departments in order to provide a comprehensive and professional service to the clients.

 The Role:

 The Senior Biostatistician is fully responsible for the end-to-end delivery of the assigned project, from both an internal and external perspective. This will include the following responsibilities:

 - Coordinate and lead a project team to successful completion of a study project

 - Interact with clients as key contact regarding all statistical and contractual matters

 - Lead production and quality control of randomisations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process-supporting documents

 - Perform QC of derived datasets and all kinds of statistical deliverables produced by other members of the department

 - Support and actively contribute to the development of client proposal documents

 - Represent at client marketing and technical meetings, both local and international

 - Proactively participate in and/or lead process/quality improvement initiatives

 - Mentor and train junior members of the department.

Experience/Qualifications required

Skills and Attributes:

 - Thorough understanding of statistical issues in clinical studies (interventional and non-interventional)

 - Excellent analytical skills and strong attention to detail

 - Ability to work independently

 - Business awareness / business development skills.

 Experience:

 This role requires a combination of statistical expertise, project management ability and excellent communication skills. We are therefore looking for someone with a strong statistical background in Clinical Research, who can really drive their project forward whilst fulfilling a pivotal role between the client and the project team. The ability to represent the company to clients is greatly desired; you will have experience in discussing complicated data in an easy to understand format while presenting a highly professional personal and corporate impression.

 In addition you will need:

 - Experience in statistical analysis in a clinically related subject, for example (Pharmaco-)Epidemiology, either academically or professionally, Outcomes Research or Health Economics

- Practical experience with SAS programming

 Qualifications:

 - Graduate or equivalent degree in Biostatistics, or Epidemiology/Pharmacoepidemiology.

Associate Director Biostatistics

Reference number: 1951 Apply for this job Apply for this job »
Type: Permanent, full time Location: Sheffield or Uxbridge

Job Description

Summary:

 Our client is a highly respected CRO which is seeking an Associate Director of Biostatistics ideally in either its Sheffield or Uxbridge offices.

 The Associate Director contributes to and leads strategic initiatives for the structure and development of the Biostatistics department in order to achieve the overall goals and mission of the company.

 The Associate Director is responsible for managing teams of statisticians involved in the production of clinical trial reports and in the provision of statistical services.

Key Accountability:

 Identify strategic needs within the Biostatistics Department

 Develop and successfully implement a plan for specific strategic initiatives

 Represent the Biostatistics Department in high-level internal initiatives

 Represent the company at client marketing and technical meetings

 Business development and the identification of new business opportunities

 Maintain and monitor budgets for non-billable spending

 Manage the recruitment process for new Biostatistics team members

 Resource planning

 Evaluate and resolve complex personnel issues

 Implement disciplinary procedures if required

 Coordinate development of client proposal documents

 Resolve client problems as and when they arise

 Consult with clients on technical, statistical or regulatory issues, as appropriate

 Provide support to Functional Lead in terms of changes in scope and contractual issues

 Provide internal technical support to the Biostatistics Department

 Develop agendas and chair departmental meetings

 Lead the development of new SOPs and guidelines as needed

 Identify the need for process and quality improvement initiatives

 Check own work in an ongoing way to ensure first time quality

Experience/Qualifications required

Skills and Attributes:

 - Financial knowledge, able to read a Profit and Loss (P&L) summary and present financial information

 - Strategic awareness of our business environment

 - Detailed awareness of the activities of other groups within the company

 - Advanced people management and leadership skills

 - Able to work with senior managers on strategic initiatives

 - Highly professional attitude

 - Attention to detail

 - Excellent analytical skills

 - Able to work under pressure and motivate others

 - Thorough understanding of statistical issues in clinical trials

 - Excellent knowledge of all statistical and reporting processes within the Biostatistics department

 - Good communication skills essential

 Qualifications:

 - Minimum of first degree (undergraduate or equivalent) in Biostatistics or another relevant discipline

Contract Biostatistician/Senior Biostatistician

Reference number: 1947 Apply for this job Apply for this job »
Type: Contract, fixed term Location: Sussex

Job Description

Summary:

 Our client is seeking a contract Biostatistician to be based in its offices in West Sussex.

 Core Responsibilities:

The provision of expert statistical input and consultancy to Phase 1-4 global clinical trials including design of clinical trials and production of analysis and reporting deliverables on behalf of and/or in conjunction with clients.

 Principal Accountabilities:

•Provide input as appropriate into all meetings, discussions and activities covering all statistical aspects for assigned trials.

•Provide statistical input (as appropriate) into study protocol and CRF to ensure that both documents meet the requirements of the study and of client(s). Ensure adherence to standards (client and/or company), relevant regulatory guidelines and the provision of good statistical practice.

•Generate and review randomisation lists and code-break envelopes in accordance with company and/or client procedures.

•Provide statistical input to the Data Management Validation Plan to ensure delivery of appropriate high quality clinical data suitable for statistical analysis and reporting.

•Author and/or provide input to trial Statistical Analysis Plans. Write detailed statistical methods according to the requirements of the protocol. Prepare table, listing and figure shells in conjunction with the Statistical Programmer(s). Chair analysis planning meetings with internal and external customers (as appropriate).

•Perform ongoing review of clinical data from company/client databases to identify potential issues with data impacting the statistical analysis.

•Program and conduct statistical analyses and provide high-quality statistical output for inclusion in clinical trial reports.

•Provide expert statistical input to clinical trial reports (as appropriate). Write statistical methods section and review results and conclusions for appropriate statistical interpretation of results.

•Responsible for quality control of all statistical analysis deliverables and quality assurance of programming deliverables provided by the company's Statistical Programmer(s) for assigned trials.

•Maintain professional and proactive interactions with internal and external customers.

•Maintain up-to-date knowledge on statistical techniques and procedures by attendance at professional courses and conferences and by ongoing review of statistical literature.

•Review the clinical database for acceptance for statistical analysis prior to database lock (as appropriate)

•Ensure maintenance and appropriate filing of trial statistical documentation for delivery to clients.

•Assist in the development of ‘best-in-class’ analysis and reporting processes to ensure operational efficiency of Biostatistics’ function.

•Support Senior Biostatisticians in the production of expert statistical input to clinical development programmes, ISS, ISE and other forms of integrated statistical analyses.

Experience/Qualifications required

Skills:

 •Knowledge/experience in SAS programming (or suitable equivalent data manipulation/statistical analysis software e.g SPSS).

•Knowledge of global clinical trial practices, procedures, methodologies.

 Experience:

 •Experience in the application of statistics in clinical trials at a CRO, pharmaceutical company or academic institution.

 

Qualifications:

 •Degree (BSc) or equivalent in Medical Statistics or Statistics/Mathematics

 Contact:

For more information or to make an application, please contact Philip North at NorthWise Services, as follows:

Telephone: +44 (0) 1795 411 571

Email: philip.north@northwiseservices.com

Senior/Principal Biostatistician

Reference number: 1945 Apply for this job Apply for this job »
Type: Permanent, full time Location: West Sussex

Job Description

Summary:

Our client is seeking an ambitious individual to join its growing Biostatistics group based in West Sussex to contribute to its statistical design, analysis and reporting services. This position can also be partly home based.

The company provides a complete statistical service, including statistical input to study design, protocol development, consultancy, planning, specifying and performing statistical analyses, conducting their write-up, and collaboration in the production of integrated study reports.

 The Role:

 You would be involved in all of the above areas, and would be responsible for statistical aspects of projects which could range in size from small early phase I trials to larger, later phase II-IV trials across a comprehensive range of therapeutic areas. In the role you would provide input to study protocols, program and conduct statistical analyses providing high quality "report ready" statistical output and critically review results and conclusions to ensure their valid and correct interpretation.

 Further, you would develop key documents, including the Statistical Analysis Plan, Quality Control and Project Conventions Plans and, working closely with the Statistical Programmers, review the derived data set specifications and trial safety data tables, listings and figures they produce. You would also be responsible for providing the statistical input into parts of the Data Management process including reviewing the eCRF (or CRF) database structure and data cleaning strategies.

Experience/Qualifications required

Skills:

 The company is looking for dynamic professionals with a depth of statistical understanding and associated clinical trials experience, as well as a sound knowledge of SAS. You will also need to be pro-active with a proven ability to work in multidisciplinary teams to agreed timelines and, most importantly, to be able to communicate effectively to both statisticians and non-statisticians alike.

  Experience:

 Minimum 3 years experience.

Proven home-based experience if partly home-based.

Relevant experience in the area of the design and analysis of clinical trials. Experience of the design and analysis of oncology studies would be desirable although not essential.

 Qualifications:

 You will have a BSc and/or an MSc in Statistics (or equivalent).

 

Contact:

For more information or to make an application, please contact Philip North at NorthWise Services, as follows:

Telephone: +44 (0) 1795 411 571


Senior Biostatistician

Reference number: 1923 Apply for this job Apply for this job »
Type: Permanent, full time Location: Sussex

Job Description

Job Description:

Our client is seeking an ambitious individual to join their growing Biostatistics group based in West Sussex to contribute to their statistical design, analysis and reporting services. This position can also be home based.

 The company provides a complete statistical service including statistical input to study design, protocol development, consultancy, planning, specifying and performing statistical analyses, conducting their write-up, and collaboration in the production of integrated study reports.

 You would be involved in all of the above areas, and would be responsible for statistical aspects of projects which could range in size from small early phase I trials to larger later phase II-IV trials across a comprehensive range of therapeutic areas. In the role you would provide input to study protocols, program and conduct statistical analyses providing high quality "report ready" statistical output and critically review results and conclusions to ensure their valid and correct interpretation.

 Further, you would develop key documents including the Statistical Analysis Plan, Quality Control and Project Conventions Plans, and, working closely with our Statistical Programmers review the derived data set specifications and trial safety data tables, listings and figures they produce. You would also be responsible for providing the statistical input into parts of the Data Management process including reviewing the eCRF (or CRF), database structure and data cleaning strategies.

Experience/Qualifications required

Candidate Requirements:

The company are looking for dynamic, professionals with a depth of statistical understanding and associated clinical trials experience, as well as a sound knowledge of SAS. You will also need to be pro-active with a proven ability to work in multidisciplinary teams to agreed timelines, and most importantly, to be able to communicate effectively to both Statisticians and Non-Statisticians alike.

 

You will have a BSc and/or an MSc in Statistics (or equivalent) and have demonstrated relevant experience in the area of the design and analysis of clinical trials. Experience of the design and analysis of Oncology studies would be desirable although not essential.

 In return, the company provides excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits.

 

This is a permanent position.

Senior Director, Global Biostatistics

Reference number: 1922 Apply for this job Apply for this job »
Type: Permanent, full time Location: Sussex

Job Description

Job Description:

Our client is looking for a Senior Director, Global Biostatistics to lead the strategic direction of their biostatistics department.

The Senior Director will manage teams and outputs over our clients four offices based in both Europe and the US.

The successful applicant will support business development activity, manage projects and liaise with partners and clients.

Experience/Qualifications required

Candidate Requirements:

The ideal candidate will have a degree in life sciences, maths or statistics or equivalent and have considerable experience in biostatistics in a global clinical research environment.

Strong leadership and communication skills are a must.

 This is a permanent position based in Sussex.