Comparative effectiveness (he / hta statistics) remote - spain & germany join cytel as an associate director, comparative effectiveness (he / hta statistics) this remote position is based in spain & germany. at cytel, you'll gain global experience in the health economics and market access environment, collaborating with multinational pharmaceutical companies, payers, clinical guidance experts, and other consultants. we are currently hiring an associate director to support our comparative effectiveness team. this role offers growth and advancement prospects, working closely with project leaders and clients on various projects. statistical modeling in health economics: survival analysis, longitudinal modeling, etc. evidence synthesis: guiding systematic literature review development for meta-analysis, meta-regression, etc. stc, maic, complex matchings, crossover analysis. consulting in he / hta statistics (~80% of work): producing high-quality indirect treatment comparisons and reports. serving as a technical advisor, guiding junior staff and clients on methods related to comparative effectiveness. preparing reports on comparative effectiveness, population matching, and other technical deliverables, including quality control. this is a technical role requiring expertise in statistics, mathematics, and regression analysis. strong writing skills are a plus. master's or phd in statistics, epidemiology, biostatistics, economics, or health economics, with 8+ years of healthcare experience (consulting, pharma, government). position level: mid-senior em...
An experienced principal biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, will lead phase i-iv clinical studies across your region. you will be dedicated to a global pharmaceutical client that is driving the next generation of patient treatment, empowering individuals to work with autonomy and ownership. our principal biostatisticians provide statistical and developmental support, influencing clinical trials by offering expertise in processes, development plans, concept sheets, and protocols. they may also oversee work supported by other vendors. you will formulate integrated analytical approaches, employing statistical methods, machine learning, and deep learning algorithms to discover actionable insights and automate processes to reduce effort and time. responsibilities include designing, running, and analyzing a/b and multivariate hypothesis tests to optimize customer and patient experience. you will work with senior data science team members to present analytical content effectively, develop automation for analysis and insights, and manage your own projects while collaborating with team members. additionally, you will independently identify research articles and apply methodologies to business problems. at cytel, we support employee success through training, development, and support. qualifications include a master’s degree in statistics or a related discipline, 9+ years supporting clinical trials in the pharmaceutical or biotechnology industry, attention to detail, excellent communication skills, and...
Comparative effectiveness (he / hta statistics) remote - spain & germany join cytel as an associate director, comparative effectiveness (he / hta statistics) this remote position is based in spain & germany. at cytel, you'll gain global experience in the health economics and market access environment, collaborating with multinational pharmaceutical companies, payers, clinical guidance experts, and other consultants. we are currently hiring an associate director to support our comparative effectiveness team. this role offers growth and advancement prospects, working closely with project leaders and clients on various projects. 1. statistical modeling in health economics: survival analysis, longitudinal modeling, etc. 2. evidence synthesis: guiding systematic literature review development for meta-analysis, meta-regression, etc. 3. stc, maic, complex matchings, crossover analysis. 4. consulting in he / hta statistics (~80% of work): producing high-quality indirect treatment comparisons and reports. 5. serving as a technical advisor, guiding junior staff and clients on methods related to comparative effectiveness. 6. preparing reports on comparative effectiveness, population matching, and other technical deliverables, including quality control. this is a technical role requiring expertise in statistics, mathematics, and regression analysis. strong writing skills are a plus. master's or phd in statistics, epidemiology, biostatistics, economics, or health economics, with 8+ years of healthcare experience (consulting, pharma, government). position level: mid-senior employ...
Comparative effectiveness (he / hta statistics) remote - spain & germany join cytel as an associate director, comparative effectiveness (he / hta statistics) this remote position is based in spain & germany. at cytel, you'll gain global experience in the health economics and market access environment, collaborating with multinational pharmaceutical companies, payers, clinical guidance experts, and other consultants. we are currently hiring an associate director to support our comparative effectiveness team. this role offers growth and advancement prospects, working closely with project leaders and clients on various projects. 1. statistical modeling in health economics: survival analysis, longitudinal modeling, etc. 2. evidence synthesis: guiding systematic literature review development for meta-analysis, meta-regression, etc. 3. stc, maic, complex matchings, crossover analysis. 4. consulting in he / hta statistics (~80% of work): producing high-quality indirect treatment comparisons and reports. 5. serving as a technical advisor, guiding junior staff and clients on methods related to comparative effectiveness. 6. preparing reports on comparative effectiveness, population matching, and other technical deliverables, including quality control. this is a technical role requiring expertise in statistics, mathematics, and regression analysis. strong writing skills are a plus. master's or phd in statistics, epidemiology, biostatistics, economics, or health economics, with 8+ years of healthcare experience (consulting, pharma, government). position level: mid-senior emp...
An experienced principal biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, will lead phase i-iv clinical studies across your region. you will be dedicated to a global pharmaceutical client that is driving the next generation of patient treatment, empowering individuals to work with autonomy and ownership.our principal biostatisticians provide statistical and developmental support, influencing clinical trials by offering expertise in processes, development plans, concept sheets, and protocols. they may also oversee work supported by other vendors.you will formulate integrated analytical approaches, employing statistical methods, machine learning, and deep learning algorithms to discover actionable insights and automate processes to reduce effort and time.responsibilities include designing, running, and analyzing a/b and multivariate hypothesis tests to optimize customer and patient experience. you will work with senior data science team members to present analytical content effectively, develop automation for analysis and insights, and manage your own projects while collaborating with team members. additionally, you will independently identify research articles and apply methodologies to business problems.at cytel, we support employee success through training, development, and support.qualifications include a master's degree in statistics or a related discipline, 9+ years supporting clinical trials in the pharmaceutical or biotechnology industry, attention to detail, excellent communication skills, and ...
Job summary: coordinate and perform data management tasks from study start up through database lock, including database set:up and data validation as per the requirements in the clinical protocols and ensure timely delivery of high:quality consistent data. lead all portions of a project/and or multiple projects with minimal or no supervision. job responsibilities: adherence to sops and maintaining audit:ready documentation. coordinate and oversee activities of all dm staff assigned to the project, ensuring high quality, respecting project timelines and adherence to the budget. attend relevant project meetings and work closely with other internal and external leads. liaise with client/partners for clarification on any clinical and / or technical decisions and propose most efficient solutions. identify risks to project deliverables and timelines, develop and implement the mitigations for these risks. create dm timelines for database set:up. lead and participate in the design of clinical electronic data capture (edc) components including mock crf, casebook, edit checks. coordinate and create data management documentation including data management plan, data validations specifications, ecrf completion guidelines, data collection system configuration, data transfer agreement. coordinate and perform user acceptance testing. train edc users. manage edc users' access and assist with resolving issues. coordinate all conduct data management tasks. lead and participate in data cleaning activities including sae and external data reconciliation. provide inpu...
Job summary: coordinate and perform data management tasks from study start up through database lock, including database set:up and data validation as per the requirements in the clinical protocols and ensure timely delivery of high:quality consistent data. lead all portions of a project/and or multiple projects with minimal or no supervision. job responsibilities: adherence to sops and maintaining audit:ready documentation. coordinate and oversee activities of all dm staff assigned to the project, ensuring high quality, respecting project timelines and adherence to the budget. attend relevant project meetings and work closely with other internal and external leads. liaise with client/partners for clarification on any clinical and / or technical decisions and propose most efficient solutions. identify risks to project deliverables and timelines, develop and implement the mitigations for these risks. create dm timelines for database set:up. lead and participate in the design of clinical electronic data capture (edc) components including mock crf, casebook, edit checks. coordinate and create data management documentation including data management plan, data validations specifications, ecrf completion guidelines, data collection system configuration, data transfer agreement. coordinate and perform user acceptance testing. train edc users. manage edc users' access and assist with resolving issues. coordinate all conduct data management tasks. lead and participate in data cleaning activities including sae and external data reconciliation. provide inpu...
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