Biostatistics Expert with Regulatory Focus

Unlocking the Power of BiostatisticsThe Senior Biostatistical Expert will lead the development of statistical methodologies and analysis plans for complex clinical trials, ensuring compliance with regulatory requirements and delivering high-quality results.Key Responsibilities:Design and implement statistical analysis plans for clinical trialsDevelop and...

About the RoleThe Senior Biostatistical Expert will provide high-level statistical support across all complexity levels of clinical trials, with a strong focus on regulatory impact.Key ResponsibilitiesDevelop and implement trial designs, protocols, and CRF configurations.Lead the production and quality control of randomization, analysis plans, statistical...

Transforming Patients' Lives Through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to discovering and developing innovative treatments for serious diseases. As a Senior Manager of Biostatistics, you will play a critical role in advancing our mission by applying your analytical skills and expertise to drive clinical trials...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a global biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Biostatistics Manager to join our team and contribute to the development of innovative treatments for serious diseases.Key Responsibilities:Collaborate with...

Working at Bristol Myers SquibbAt Bristol Myers Squibb, we are inspired by a single vision – transforming patients' lives through science. In oncology, hematology, cell therapy, 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...

Transforming Patient Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patient lives through science. As a Senior Manager of Biostatistics, you will be part of a cross-functional development team, contributing to trial design, protocol development, analysis planning, result interpretation, and regulatory...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a company that is dedicated to transforming patients' lives through science. We are inspired by a single vision - to make a meaningful difference in the lives of patients. In oncology, hematology, cell therapy, immunology, and cardiovascular disease, our passionate colleagues...

Key ResponsibilitiesAs a Principal Biostatistician at Parexel, you will work independently on complex clinical trial projects with significant regulatory impact. You will be recognized as a statistical expert both internally and externally.Operational ExecutionProvide statistical support for trial design, protocol, and CRF development on specific...

Key Responsibilities Provide statistical support for trial design, protocol, and CRF development. Lead production and quality control of randomization, analysis plans, statistical reports, and other process supporting documents. Perform sample-size calculations, generate randomization lists, and write statistical methodology sections for study protocols....

Job TitleRegulatory Affairs Expert - Enhanced Regulatory ComplianceAbout the RoleThis exciting opportunity is part of a globally inclusive and diverse company, Eastman Chemical Company. As a Regulatory Affairs Expert, you will be responsible for resolving complex regulatory challenges and initiatives for Eastman's product portfolio.Your primary focus will be...

Transformative Regulatory Solutions at Bristol Myers SquibbBristol Myers Squibb is an innovative leader in the pharmaceutical industry, dedicated to creating a brighter future for patients worldwide. Our mission is to deliver transformative medications that improve lives and expand possibilities.Salary Range: $80,000 - $120,000 per yearWe are seeking a...

Bristol Myers Squibb is a global biopharma leader driven by a mission to transform patients' lives.Estimated Salary: $120,000 - $180,000 per yearAbout the RoleWe are seeking an experienced Regulatory Submission Manager to join our team in Hyderabad. The successful candidate will be responsible for managing and coordinating the timely, compliant, and accurate...

Thomson Reuters ONESOURCE University is seeking an experienced Tax and Regulatory Expert to join our global team in India.In this role, you will deliver training (primarily live remote and occasionally on-site) to clients of ONESOURCE Corporate Tax and related tax technology software solutions. You will work closely with clients and Thomson Reuters teams...

About this RoleWe are seeking a highly skilled Senior Regulatory Content Expert to join our team at Lifelancer. In this role, you will be responsible for creating and editing high-quality clinical and safety documents for submission to regulatory authorities.Key Responsibilities:Write and/or edit complex Clinical Study Reports (CSR), CTD submission...

Job Description for Associate Director Statistical ProgrammingBristol Myers Squibb is seeking an exceptional Associate Director to lead our Statistical Programming team in the development, regulatory approval, and market acceptance of our innovative products.Key Responsibilities:Design, develop, and implement technical solutions for integrating, analyzing,...

Sentient Solutions for Accounting is a rapidly growing outsourcing firm, offering customized solutions to CPA Firms across the United States. Our team of experts, based in the US, India, and Mexico, utilizes AI and process automation to provide scalable services.We are seeking a Tax Senior to join our team. As a Tax Senior, you will work independently and...

At Corteva Agriscience, we are seeking an experienced Regulatory Compliance Expert to join our team as a Dangerous Goods Analyst.We are looking for a highly skilled professional who can ensure continued compliance and efficiency within the dangerous goods space by collaborating with our internal teams and business partners.Job OverviewThis role involves...

Parexel seeks a highly skilled Regulatory Affairs Specialist to join our team in this exciting role. With a focus on biologics, you will be responsible for handling pre and post-approval life cycle management of drug products.About the RoleIn this challenging and rewarding position, you will have the opportunity to utilize your knowledge of regulatory...

About the OpportunityWe are seeking an experienced Global Medical Expert to join our team at Lifelancer in a regulatory lead role. This is a fantastic opportunity for someone with a strong background in medical affairs, clinical development, and pharmacovigilance.Job DescriptionProvide medical assessment with relevant and updated clinical evidence to support...

About the JobWe are seeking a highly skilled Senior Regulatory Affairs Specialist- Q&R to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT. As a key member of our regulatory affairs function, you will play a critical role in ensuring compliance with global regulations and maintaining the highest standards of...