Wir verwenden Cookies, um die Benutzererfahrung zu verbessern, den Verkehr zu analysieren und relevante Anzeigen anzuzeigen.
Mehr Annehmen
Position eingeben

Gehaltsübersicht für Senior Statistical Programmer in Schweiz

Erhalten Sie Statistikinformationen per E-Mail

Gehaltsübersicht für Senior Statistical Programmer in Schweiz

18 400 ₣ Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Senior Statistical Programmer in Schweiz"

Währung: CHF USD Jahr: 2021
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Senior Statistical Programmer Branche in Schweiz

Verteilung des Stellenangebots "Senior Statistical Programmer" in Schweiz

Währung: CHF
Wie die Grafik zeigt, in Schweiz gilt Kanton Neuenburg als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kanton Zug. Den dritten Platz nimmt Kanton Zürich ein.

Ranking der Kantone in Schweiz gemäß dem Gehaltsniveau für den Beruf "Senior Statistical Programmer"

Währung: CHF
Laut der Statistik unserer Webseite ist Senior Statistical Programmer der bestbezahlte Beruf in Kanton Genf. Die Fachkraft verdient durchschnittlich 20000 CHF. Als nächstes folgt Basel-Landschaft and Basel-Stadt.

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Schweiz

Währung: CHF
Unter den ähnlichen Berufen in Schweiz gilt Personal Assistant als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 87500 CHF. An zweiter Stelle folgt Réceptionniste mit dem Gehalt von 72000 CHF und den dritten Platz nimmt Directeur mit dem Gehalt von 69058 CHF ein.

Empfohlene Stellenangebote

Senior or Principal Statistical Programmer
Cytel, Genf
Senior or Principal Statistical Programmer Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. We are currently looking for technically skilled and experienced Sr. Statistical Programmers to support a client's programming activities within their Full Development projects. How you will contribute: Work together with our customer's statistical and programming teams on projects Contribute to pooled ADaM dataset specification, creation and output programming for ISS/ISE, safety update reports, Health Authority requests etc. Participate in programming activities for adhoc analyses, publication, Health Technology Assessment (HTA), Health Economics etc. Ensure quality and timeliness of own deliverables as well as good planning and management of team deliverables Communicate effectively with the related stakeholders Contribute to technical or other initiatives, mentor new joiners or more junior programmers, give presentations in internal team meetings etc. as appropriate What you offer: Bachelor degree in Statistics, Life Sciences, Computer Sciences or similar field. Master's level preferred 5 or more years of statistical programming working with clinical trial and other medical data Strong proficiency in SAS applied to clinical trial and other medical data Experience in both structured (clinical trial and project) work as well as in less structured post-marketing/adhoc environments is preferred Strong team player who also has experience in leading a team effort Knowledge of CDISC, in particular ADaM and reporting standards Proactive approach and independent learning capabilities, with contextual understanding beyond being "spoon-fed" instructions Good analytical and troubleshooting skills Flexible and adaptive as well as systematic in ensuring quality of deliverables Experience with project-level deliverables (ISS/ISE, submission, safety reports etc.) and adhoc work is a plus Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. Meaningful Work, Collaborative Culture, Stimulating Challenges Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry. In addition to a competitive compensation, we offer an excellent benefits package, annual bonus incentive, promote work-life balance, and the opportunity to grow with us Work with respected experts and thought leaders in the fields of biostatistics and statistical programming. LI-CR1 Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law. Cytel does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Cytel’s human resources department to obtain prior written authorization before referring any candidates to Cytel. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Cytel. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Cytel. Cytel shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies.
Senior Manager, Biostatistics
Bristol Myers Squibb Company, Boudry, Switzerland
Senior Manager, Biostatistics At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Purpose: The Senior Manager Biostatistician is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Statisticians develop collaborative relationships and work effectively with the GBDS Biostatistics Lead, the GBDS Planning and Execution Lead, GBDS programmer, medical monitor, protocol manager, data manager, PK scientist, and other members of the study/indication team. Primary Responsibilities: Ensures that all analyses conducted have clearly articulated hypotheses associated with them and that the trial design and data collected support conducting the analysis Communicates effectively with clinical and regulatory partners Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, dataset specifications, case-report forms, randomization specifications, clinical study reports, associated publications and other study level specification documents Exercises cost-disciplined science in sizing of the trials and in the planning for the analyses to be conducted Compliant with BMS processes and SOPs, global and project standards, and responsible for quality of deliverables Ensures programming team or vendor partner understands the nature of the clinical data being collected and the approaches to summarizing the information Collaborates with clinicians and medical writers to prepare summaries of results for use in regulatory documents and scientific articles Drives, with the Clinician, the interpretation of results, development of key messages and communication to the development team. Provides statistical consultation for ad hoc analysis requests including design of appropriate analyses to answer relevant questions Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. Education/Experience: Significant academic training in statistics, biostatistics or relevant areas of study. PhD degree in statistics or biostatistics or Master's degree with relevant experience required. Understanding of the application of biostatistics to medical/clinical trials data. SAS experienced level, R expertise desirable. Familiar with nQuery, EAST or other software for sample size calculations. Experience with Bayesian methodology, meta-analysesand with RWD analyses desirable. Familiar with survival analyses, time to event analyses, efficacy endpoints in oncology (ORR, etc) in Phase II, III trials. Familiar with clinical pharmacology trials (PK analysis, bioequivalence designs, etc.). Experience with aggregated safety analyses desirable. Familiar with SDTM/ADAM. Ability to work successfully within cross-functional teams leading to successful global regulatory filings and approvals Excellent verbal and written communications skills (English). Ability to be flexible and adapt quickly to the changing needs of the organization. Ability to organize multiple work assignments and establish priorities. Strong interpersonal skills evidenced in interactions with individuals at all levels of the organization, and demonstrated ability to develop relationships within the organization and leverage the formal and informal organizational structure to assist in goal achievement. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Senior Manager, Biostatistics
Bristol Myers Squibb, Boudry, Neuenburg
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Purpose: The Senior Manager Biostatistician is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Statisticians develop collaborative relationships and work effectively with the GBDS Biostatistics Lead, the GBDS Planning and Execution Lead, GBDS programmer, medical monitor, protocol manager, data manager, PK scientist, and other members of the study/indication team. Primary Responsibilities: Ensures that all analyses conducted have clearly articulated hypotheses associated with them and that the trial design and data collected support conducting the analysis Communicates effectively with clinical and regulatory partners Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, dataset specifications, case-report forms, randomization specifications, clinical study reports, associated publications and other study level specification documents Exercises cost-disciplined science in sizing of the trials and in the planning for the analyses to be conducted Compliant with BMS processes and SOPs, global and project standards, and responsible for quality of deliverables Ensures programming team or vendor partner understands the nature of the clinical data being collected and the approaches to summarizing the information Collaborates with clinicians and medical writers to prepare summaries of results for use in regulatory documents and scientific articles Drives, with the Clinician, the interpretation of results, development of key messages and communication to the development team. Provides statistical consultation for ad hoc analysis requests including design of appropriate analyses to answer relevant questions Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. Education/Experience: Significant academic training in statistics, biostatistics or relevant areas of study. PhD degree in statistics or biostatistics or Master’s degree with relevant experience required. Understanding of the application of biostatistics to medical/clinical trials data. Familiar with nQuery, EAST or other software for sample size calculations. Experience with Bayesian methodology, meta-analyses and with RWD analyses desirable. Familiar with survival analyses, time to event analyses, efficacy endpoints in oncology (ORR, etc) in Phase II, III trials. Familiar with clinical pharmacology trials (PK analysis, bioequivalence designs, etc.). Experience with aggregated safety analyses desirable. Familiar with SDTM/ADAM. Ability to work successfully within cross-functional teams leading to successful global regulatory filings and approvals Excellent verbal and written communications skills (English). Ability to be flexible and adapt quickly to the changing needs of the organization. Ability to organize multiple work assignments and establish priorities. Strong interpersonal skills evidenced in interactions with individuals at all levels of the organization, and demonstrated ability to develop relationships within the organization and leverage the formal and informal organizational structure to assist in goal achievement. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Senior Manager, Biostatistics
Bristol Myers Squibb, Boudry, Neuenburg
Purpose: The Senior Manager Biostatistician is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Statisticians develop collaborative relationships and work effectively with the GBDS Biostatistics Lead, the GBDS Planning and Execution Lead, GBDS programmer, medical monitor, protocol manager, data manager, PK scientist, and other members of the study/indication team. Primary Responsibilities: Ensures that all analyses conducted have clearly articulated hypotheses associated with them and that the trial design and data collected support conducting the analysis Communicates effectively with clinical and regulatory partners Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, dataset specifications, case-report forms, randomization specifications, clinical study reports, associated publications and other study level specification documents Exercises cost-disciplined science in sizing of the trials and in the planning for the analyses to be conducted Compliant with BMS processes and SOPs, global and project standards, and responsible for quality of deliverables Ensures programming team or vendor partner understands the nature of the clinical data being collected and the approaches to summarizing the information Collaborates with clinicians and medical writers to prepare summaries of results for use in regulatory documents and scientific articles Drives, with the Clinician, the interpretation of results, development of key messages and communication to the development team. Provides statistical consultation for ad hoc analysis requests including design of appropriate analyses to answer relevant questions Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. Education/Experience: Significant academic training in statistics, biostatistics or relevant areas of study. PhD degree in statistics or biostatistics or Master’s degree with relevant experience required. Understanding of the application of biostatistics to medical/clinical trials data. Familiar with nQuery, EAST or other software for sample size calculations. Experience with Bayesian methodology, meta-analyses and with RWD analyses desirable. Familiar with survival analyses, time to event analyses, efficacy endpoints in oncology (ORR, etc) in Phase II, III trials. Familiar with clinical pharmacology trials (PK analysis, bioequivalence designs, etc.). Experience with aggregated safety analyses desirable. Familiar with SDTM/ADAM. Ability to work successfully within cross-functional teams leading to successful global regulatory filings and approvals Excellent verbal and written communications skills (English). Ability to be flexible and adapt quickly to the changing needs of the organization. Ability to organize multiple work assignments and establish priorities. Strong interpersonal skills evidenced in interactions with individuals at all levels of the organization, and demonstrated ability to develop relationships within the organization and leverage the formal and informal organizational structure to assist in goal achievement.
Senior Statistical Programmer Analyst
, Basel
Senior Statistical Programmer Analyst Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Statistical Programmer Analyst within Janssen Research & Development (JRD), to be located in High Wycombe UK, or Leiden, Netherlands; Beerse, Belgium; Basel, Switzerland; France; Germany or Ukraine At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are proactively working to create a world without disease. Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us! We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with th
Senior Clinical Programmer
Johnson & Johnson, Basel, CH
Senior Clinical Programmer Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Clinical Programmer within Janssen Research & Development (JRD), to be located in High Wycombe UK, or Leiden, Netherlands; Beerse, Belgium; Basel, Switzerland; France; Germany or Ukraine At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us! We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone