... teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis. Your Responsibilities: Design and implement statistical strategies for clinical trials within various therapeutic areas. Develop ...
... a highly experienced and motivated Clinical Trials Lead Programmer to join our ... programming technology and techniques, clinical trials, and developments in the pharmaceutical ... at least 6 years of clinical trial experience as a statistical programmer ...
... a highly experienced and motivated Clinical Trials Lead Programmer to join our ... programming technology and techniques, clinical trials, and developments in the pharmaceutical ... at least 6 years of clinical trial experience as a statistical programmer ...
... teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis. Your Responsibilities: Design and implement statistical strategies for clinical trials within various therapeutic areas. Develop ...
... members of the group : * For clinical trial protocols under the ownership of ... of the protocol. o For clinical trial protocols under the ownership of ...
... working with the physicians within Clinical Development to provide clinical research support for programs as ... at least 5 years as clinical research scientist in oncology are ... ,000 Sites and 675,000+ Trial patients. No matter what your ...
... Review Board (IRB) submissions Manage trial master files, budgets, and agreements ... of study databases for managing clinical data Monitor and analyze clinical study data and report on ... FDA) laws and guidance on clinical studies Strong working knowledge of ...
... working with the physicians within Clinical Development to provide clinical research support for programs as ... at least 5 years as clinical research scientist in oncology are ... ,000 Sites and 675,000+ Trial patients. No matter what your ...
... and technologies to supply clinical trial materials to patients.brbrBusiness areabrIn the Clinical Supply Quality Team, we are ... the development of new Clinical Trials and collaborations and the supply ... up for global clinical studies working with a variety ...
... Review Board (IRB) submissions Manage trial master files, budgets, and agreements ... of study databases for managing clinical data Monitor and analyze clinical study data and report on ... FDA) laws and guidance on clinical studies Strong working knowledge of ...