7 Trial Design Jobs

Role Overview: You will play a key role in developing clinical database products in various therapeutic areas such as Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory, etc. Your primary focus will be to ensure the high quality of these products to support Meta-analysis. Additionally, you will be responsible for analyzing and annotating trial design information, treatments, demographics, and outcomes data from clinical literature. Your role will also involve digitizing results from graphs and working closely with the team to understand and contribute to database rules and quality processes. Key Responsibilities: - Develop clinical database products with high quality to support ...

As the Manager of Biostatistics at Bristol Myers Squibb, you will be a valuable member of cross-functional study/project teams, contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. You will develop collaborative relationships and work effectively with the Biostatistics Lead and other cross-functional team members. **Key Responsibilities:** - Member of cross-functional study/project teams - Collaborate with team members for effective project outcomes - Contribute to optimizing production line and breakthroughs in cell therapy **Qualifications Required:** - Strong background in biostatistics or related fiel...

Role Overview: The ideal candidate for the Biostatistician role should possess a Master's degree in Statistics or equivalent. A Ph.D. in Statistics or equivalent combined with 6 years of industry-related experience is also a preferred qualification. With at least 9+ years of experience, you must demonstrate a deep understanding of statistical and clinical trials methodology as it pertains to clinical development. As a Biostatistician, you will be an integral part of cross-functional development teams, contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Your role will involve collaborating with various st...

Role Overview: As a Senior Clinical Research professional at Ascentrik Research Pvt. Ltd, you will be responsible for leading and managing a research team to curate accurate, timely, insightful, and comprehensive data and intelligence for Beacon Targeted Therapies. You will work closely with UK-based clients, analyze relevant information, and ensure project deliverables are met. Additionally, you will be part of a global network of life science researchers, focusing on dynamic products in cutting-edge life science areas. Key Responsibilities: - Lead and manage a research team to curate accurate, timely, insightful, and comprehensive data and intelligence - Identify and analyze the most relev...

You are an experienced Associate Director - Biostatistics who will be joining a leading client in the pharmaceutical industry. Your role will be crucial in clinical development, involving tasks such as contributing to trial design, analysis planning, interpretation of results, and regulatory submissions. Your key responsibilities will include collaborating on innovative and efficient clinical trial designs to ensure alignment with study objectives. You will independently author and review protocols, statistical analysis plans, and clinical study reports. Providing statistical leadership in regulatory interactions, publications, and presentations will also be part of your role. Additionally, ...

You will be playing a key role in developing clinical database products across various therapeutic areas such as Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory with a focus on high quality to support Meta-analysis. Your responsibilities will include analyzing and annotating trial design information, treatments, demographics, and outcomes data from clinical literature sources. You will also be required to digitize results from graphs accurately and consistently. Collaboration will be a key aspect of your role as you work with lead consultants, peer data analysts, and quality managers to contribute to database rules, specifications, and quality processes. Additionally, you...

Role : Centralized Monitoring Assistant Skill : Must have Good Clinical Practices (GCP) Mode : Hybrid (3 Days Work from Kochi office & 2 days from HOME) Experience : 0.6 Month to max 3 years of Exp Only. Job Location : Kochi and Ahmedabad Educational Qualification: Graduate/Post Graduate in Life Sciences PURPOSE • Engage in company training program to gain knowledge and skills required to provide administrative support to • projects in accordance with SOPs, policies, good clinical practices, and applicable regulatory requirements. • Meeting quality and timeline metrics under direction of line manager and/or other designated team members RESPONSIBILITIES Complete appropriate role-specific tra...