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:
Data Managers
Statistical Programmers
Statisticians
Quality Management Experts
IT-Experts
for freelance and permanent positions. Find out more below.
Data Management
We are offering permanent or freelance positions as Data Manager (all genders). Candidates with all experience levels are encouraged to apply.
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Responsibilities
- Development and maintenance of clinical data management documents (e.g., data management plan, data review plan)
- Maintenance of eTMF
- Creation of CRF including annotations
- Design and setup of clinical databases
- Creation of validation specifications
- Programming of edit checks
- Review of data and query management
- Preparation of data transfer specifications and their conduct (e.g., IRT, external laboratory data)
- Conduct of database lock
- Application of industry standards (e.g., CDISC, coding dictionaries)
- Collaboration with technical and clinical team members (e.g., CRAs, drug safety specialists, statisticians) throughout the clinical trial planning, conduct, and reporting
- Contribution to continuous improvement
- Development and enhancement of processes (SOPs)
Qualifications
- Bachelor’s degree or equivalent in medical documentation, computer science, data engineering, or a related field
- Strong interest in clinical research
- Expertise in clinical EDC systems (Rave and Veeva preferred)
- Experience in one or more programming languages (particularly SAS and SQL)
- Fluency in English
Benefits
- Flexible work structure, full or part-time
- Option to work in Sulzbach, Marburg, or 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.
Statistical Programming
We are offering permanent or freelance positions as Statistical Programmer (all genders). Candidates with all experience levels are encouraged to apply.
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Responsibilities
- 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)
Qualifications
- 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
Benefits
- Flexible work structure, full or part-time
- Option to work in Sulzbach, Marburg, or 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 permanent or freelance positions as Statistician (all genders). Candidates with all experience levels are encouraged to apply.
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Responsibilities
- 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
- 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
- Participation in industry working groups, conferences, and scientific meetings
- Development of standard operating procedures (SOPs) and contribution to continuous improvement
Qualifications
- Masters’ or equivalent/higher degree in Biostatistics, Mathematics, Biometry, or similar subject
- Strong knowledge in statistical methodology
- Analytical and problem-solving skills
- Expertise in one or more programming languages (particularly SAS and 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
- Excellent English verbal and written communication skills
Benefits
- Flexible work structure, full or part-time
- Option to work in Sulzbach, Marburg, or 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.