Career

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Our mission

mainanalytics offers high-quality services to clinical trial sponsors – from world-leading pharmaceutical companies over innovative biotechs to well-known research institutes – and supports diverse tasks in the field of drug development and clinical studies. We work on global projects driven by the desire for medical advancement and improved well-being of patients. As enthusiastic experts we collaborate closely with clinical research specialists from various disciplines.

We aim for progress

Our team supports the development of new medications and the improvement of already existing treatments. We engage with passion to help building a healthier world. In our dynamic and international working environment, we are always interested in meeting new talents. If you want to be part of our clinical data analysis team at one of the most intercultural and energetic locations in Europe, we look forward to receiving your application: apply@mainanalytics.de

Professionals welcome

We are a diverse and multinational team – from young talents to professionals with more than 25 years of experience. We believe that innovation comes from a good mixture of solid expertise and inspiring ideas. If you are an expert in clinical data analysis looking for new challenges: send us your application.

Vacancies

We are always accepting applications for:
Statistical Programmers
Statisticians
Quality Management Experts
IT-Experts
for freelance and permanent positions. Find out more below.

Statistical Programming

We are offering a permanent or freelance position as Statistical Programmer (m/f/d) for our locations in Sulzbach (Frankfurt/Main) and Marburg, or home-based.

Share:
  • Development and validation of analysis datasets, tables, listings, and figures for various purposes (e.g. Clinical Trial Report, interim analyses, publications, regulatory requests)
  • Harmonization of data across trials for project-level purposes
  • Participation in review process of clinical trial documents, e.g. statistical analysis plans and table shells
  • Application of industry standards (e.g. CDISC)
  • Collaboration with other trial team functions (such as data management, statistics, or medical writing) throughout the clinical trial conduct and analysis
  • Development of standard programs and tools as well as statistical programming processes and standards (SOPs)
  • Bachelor’s degree or equivalent in a technical or scientific area, with a strong quantitative background
  • Strong interest in clinical data analysis
  • Experience in one or more programming languages (particularly SAS or R) preferred
  • Willingness to further develop programming skills is required
  • Ability to complete project-related tasks (e.g. participating in meetings and compile specifications) in English
  • German skills or willingness to learn German is a plus
  • Background in statistics or biostatistics and GCP environment preferred
  • Candidates with all experience levels are encouraged to apply
  • Flexible work structure
  • Options to work remotely
  • Flat hierarchy
  • Collaborative and positive team spirit
  • Dedicated resources for further professional development

We look forward to receiving your application. For any questions or to apply, please contact apply@mainanalytics.de.

Biostatistics

We are offering a permanent or freelance position as Statistician (m/f/d) for our locations in Sulzbach (Frankfurt/Main) and Marburg, or home-based.

Share:
  • Analysis, and reporting of clinical trials and preparation of integrated summaries
  • Authoring of Statistical Analysis Plans (SAP) including design of table, listing and graph (TLG) shells
  • Input to dataset specifications and review of outputs for analysis and reporting of pre-clinical/clinical trials or pooled analyses
  • Quality control (QC) of programmed files used for the reporting of clinical trials, preparation of submission dossiers, ad hoc requests by health authorities, or publications
  • Statistical input to clinical trial reports, integrated summaries and (e)CTDs
  • Collaboration with other trial team functions (such as data management, statistical programming, pharmacovigilance, clinicians, or medical writing) throughout the clinical trial conduct and submission preparation
  • Communication and presentation of statistical methodology and analysis results to clients, investigators, regulatory authorities, scientific communities, and non-statisticians (e.g., clinicians)
  • Contribution to (medical) publications
  • Training of team members on statistical methodology, processes, and tools
  • Participation in industry working groups, conferences, and scientific meetings
  • Development of standard operating procedures (SOPs) and contribution to continuous improvement
  • Masters’ or equivalent/higher degree in Statistics, Biostatistics, Mathematics, or similar subject
  • Strong knowledge in statistical methodology
  • Analytical and problem-solving skills
  • Expertise in one or more programming languages (particularly SAS and/or R)
  • Experience in clinical research and working in a strongly regulated environment (GCP) preferred
  • Strong interest in clinical data analysis
  • Flexibility to work independently and as part of a team and to interact with multidisciplinary scientists
  • Ability to focus on accurate and timely completion of project-related and competing tasks
  • Willingness to (further) develop knowledge of industry standards and new statistical methodology
  • Excellent English verbal and written communication skills
  • Flexible work structure
  • Option to work remotely
  • Flat hierarchy
  • Collaborative and positive team spirit
  • Dedicated resources for further professional development

We look forward to receiving your application. For any questions or to apply, please contact apply@mainanalytics.de.

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