6.0 - 10.0 years

0 Lacs

karnataka

On-site

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...

Posted 2 weeks ago

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Senior Clinical Research Associate Ascentrik

2.0 - 6.0 years

0 Lacs

pune, maharashtra

On-site

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...

Posted 3 weeks ago

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Director Biostatistics Pharma

8.0 - 12.0 years

0 Lacs

hyderabad, telangana

On-site

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, ...

Posted 1 month ago

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Data Analyst Level 1 Certara

1.0 - 5.0 years

0 Lacs

hyderabad, telangana

On-site

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...

Posted 1 month ago

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Centralized Monitoring Assistant IQVIA

1 - 3 years

1 - 3 Lacs

Kochi

Work from Office

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...

Posted 4 months ago

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