Senior Biometrician Job in Switzerland

Mylene Paumier at CK Clinical is recruiting for a Senior Biometrician to join a global pharmaceutical company at their site based in Switzerland on a permanent basis.

Senior Biometrician Job Description:

As Senior Biometrician, your responsibilities will include the following:

  • Be responsible and accountable for transcribing MAP aligned RAPs into computational solutions for the statistical programmer to implement (specifications of derived variables, specification and development of statistical computing solutions for inferential statistical analyses, tables and listings templates, and modern statistical graphics for the FIR and CSR) of Phase I-IV clinical trials
  • Be responsible and accountable for multiple studies RAP execution including the RAP meetings with the necessary CTT members, reporting activities, exploratory analyses/ graphics and additional analyses to support publications for individual clinical trials
  • Ensure that documents, specifications, programs/macros are consistent and comply with CSU/project/company standards/processes and provide operational input into VAPs, specifications of analysis datasets, listings, tables and figures, CSR for Phase I-IV clinical trials ensuring that consistent practices across multiple studies is kept
  • Attend CTT/GCT meetings to help facilitate decision making during design, conduct and reporting of clinical results

Qualifications, Skills and Experience:

As Senior Biometrician, you will have the following qualifications, skills and experience:

  • MS (in Statistics or equivalent) with relevant work experience or PhD (in Statistics or equivalent) with no work experience
  • Working knowledge of/experience with SAS/ R/ Splus or any other business or research analytic software with an expertise in at least one software
  • Statistical and numerical knowledge and expertise in analytic aspects
  • Good knowledge of data architecture
  • Excellent interpersonal and communication skills

How to apply:

Mylene Paumier - Biometrics Recruitment in Switzerland at CK Clinical

Please contact Mylene for more details.

Click here to apply online now.

For more information regarding this Senior Biometrician position, please contact Mylene Paumier on 01438 743047 or email: Please quote reference CL24415 in all correspondence.

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Director, Biostatistics – South East

Priya Mukherjee at CK Clinical is currently recruiting for a Director, Biostatistics to join a leading pharmaceutical organisation at their site in the South East.

The Job:

The purpose of this Director,Biostatistics role is to collaboratively produce and support critical data-based evidence for assertions and label claims about medicines through all Phases (I-IV, NIS, IIT) covering biomarkers, efficacy, safety, PRO/QOL and HEOR HEOR for simple and complicated trial designs and challenging analyses.


As a Director, Biostatistics you will

  • Handle the day-to-day operational managerial role of single EU Biostatistics team integrated over UK and Germany delivering a regional tactical focus with strong global liaison on a coordinated joint delivery with other regions – across various therapeutic areas including oncology, cardiovascular and metabolic.
  • Through strategic leadership in project teams, you will add value to the company by accelerating worldwide product approvals and enhancing EU product market share and appeal.
  • Enhance functional technical expertise in designing, driving and delivering high quality objective core contributions at the heart of the EU drug development and commercialisation process together with the required ‘state-of-the-art’ regional and global infrastructure.
  • Lead a regional Biostatistics group who oversees all project related biostatistical activities.
  • Develop, directs, prioritises and monitors all statistical programs and processes relevant to clinical trial design, data collection and input, data analysis, data display, QC, and reporting of results with the primary purpose of accelerating worldwide product submissions and investigational product approvals.
  • Oversees and monitors project timelines to ensure established corporate target dates are met.
  • Encourage, monitor, and facilitate biostatistical activities and interactions between international sites, towards the development and implementation of global statistical analysis and reporting standards.
  • Review of all clinical trial protocols, clinical trial reports, and analysis deliverables
  • Ensure quality of all deliverables related to data analysis, display, and reporting of clinical trial results.
  • Provide close interaction with cross-functional groups in the review and selection of CROs; develops and reviews CRO contracts; tracks CRO milestone, timelines, and issues; resolves same.
  • Develop long-range plans for the future of Biostatistics, and monitors metrics and evaluates staff performance. Manages and develops the technical competence and careers of the biostatistical staff.
  • Provide leadership to Biostatistics in setting short-term and long-term departmental, project, and professional goals and objectives.
  • Create momentum, energy, and opportunities for visibility of group within corporate and functional settings.
  • Expand support to new areas and builds new cross-functional relationships while solidifying and enhancing existing relationships.

Qualifications and skills:

The successful application for this Director – Biostatistics job will have the following skills and qualifications:

  • A Ph.D in Statistics, Biostatistics or Mathematics (OR Equivalent).
  • Proven Pharmaceutical Industry experience, together with proven supervisory/management and project management experience.
  • Exposure to vendor risk and performance management, compliance and oversight.
  • Good oral and written communication skills.
  • Proficient in Microsoft Office Suite including Word, Excel, and Project
  • Demonstrated problem solving, analytical, organization, and time management skills
  • Excellent managerial skills; coaches, guides, and professionally develops direct reports
  • Exhibits customer focus, flexibility and team spirit
  • Ability to lead and influence others
  • Demonstrated experience in leading remote teams
  • Ability to function effectively in different cultural settings
  • Proven experience in the implementation of electronic data capture (EDC)

How to apply:Priya Mukherjee - Senior Consultant at CK Clinical

Apply online:

For more information or to apply for this Director – Biostatistics role please contact Priya Mukherjee on 01438 743 047 or email Please quote reference CL24311 in all correspondence.

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Associate Director Biostatistics Job in UK

Priya Mukherjee at CK Clinical is currently recruiting for an Associate Director Biostatistics to join a successful pharmaceutical company in the UK.

As Associate Director Biostatistics you will work as part of the Biostatistics and Statistical Programming, Clinical Department Operations and Biometrics function. You will be joining an expanding team within the Specialty Pharmaceutical portfolio of products in R&D where you will contribute to product development strategy and serve as a project lead.

As Associate Director Biostatistics your main responsibilities will include:

  • You will manage statistical issues in communications with regulatory authorities and author statistical sections of protocols and statistical analysis plans.
  • You will contribute to regulatory documents, publication materials, and provide expert statistical consulting to development teams while working with vendors.
  • You will lead a program of global Phase I-IV studies

To be considered for this Associate Director Biostatistics role you will hold relevant academic qualifications or equivalent (BSc / MSc / PhD) in Biostatistics or a Scientific discipline and have previous relevant experience from a Pharmaceutical or CRO environment in a similar lead position.

You will also hold excellent communication, project management and leadership skills with the ability to work in a matrix model, together with the ability to build strong relationships that are results and quality focused.

How to apply:

Click here to apply online now.

For more information regarding this Associate Director Biostatistics, please contact Priya Mukherjee at CK Clinical on +44(0)1438 870028 or email Please quote reference CL23912 in all correspondence.

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Director of Biostatistics Job in the Midlands

Priya Mukherjee is recruiting for a Director of Biostatistics to join a leading company based in the Midlands.

Director of Biostatistics Job Description:

As Director of Biostatistics, you will lead the Biostatistics Department in providing statistical services for clinical trials. Your responsibilities will include:

  • To provide leadership of the Biostatistics Department, co-ordinating and assisting staff in their duties.
  • To be responsible for staff allocation within the department, to ensure sufficient expertise and to delegate responsibility appropriately.
  • To identify the departmental training requirements and to provide training as required.
  • To perform staff reviews.
  • To represent the Biostatistics department at internal meetings and to liaise with in-house project managers and fellow departmental heads.
  • To provide statistical advice/consultation and/or any related services required by Sponsors.
  • To lead projects on behalf of the Company.
  • To represent the Company and participate at meetings and conferences.
  • To be responsible for statistical software administration for the Company.
  • Additionally, the job holder is expected to perform all duties associated with the post of Senior Statistician.
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

As Director of Biostatistics, you will have the following skills, experience and qualifications:

  • Experienced in working closely with Sponsors, and have good communication skills in order to provide clear statistical advice.
  • Experience co-ordinating the workloads of other staff and possess good time-management skills.
  • A thorough knowledge of statistics.
  • Computer literate with a willingness to adapt to various computer systems; a detailed knowledge of SAS, and other related software is essential.

Interested applicants will be educated to degree level in mathematics, statistics or another subject with a strong statistical component (OR Equivalent) and have proven experience using statistics in a clinical research environment, including SAS programming. You should also be able to demonstrate a high level of competency, responsibility, and the ability to work independently.

How to apply:

Click here to apply online now.

For more information, please contact Priya Mukherjee at CK Clinical on +44(0)1438 870028 or email Please quote reference CL23605 in all correspondence.

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