We have other current jobs related to this field that you can find below
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Senior Biostatistician
2 months ago
London, United Kingdom Luminary Group Full timeLuminary Group is currently seeking a skilled and dedicated Principal Biostatistician to join our client. As a Biostatistician, you will play a crucial role in providing statistical support and expertise for research studies and clinical trials. You will collaborate with cross-functional teams to analyze, interpret, and report study data, contributing to the...
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Senior Biostatistician
2 weeks ago
London, United Kingdom Warman O'Brien Full timeSenior / Principal Biostatistician - CRO - UK/Remote We have recently partnered with this modern thinking, CRO, who are looking for biostatisticians to join their team, to expand their outreach in the UK / Europe.Key Accountabilities:Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or...
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Principal Biostatistician
1 month ago
London, United Kingdom Hobson Prior Full timeHobson Prior is seeking a Principal Biostatistician to join our team. This role involves overseeing statistical activities on projects, including study designs, statistical methodologies, and reporting. You will also work with various teams to contribute to the strategic element of projects and interact with regulatory authorities.Please note that to be...
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Principal Biostatistician
3 months ago
London, United Kingdom Novartis Full time**Summary**: 15 months rotating across 3 key areas of the Novartis Analytics OrganizationNovartis continues to accelerate its growth in the data and digital space. As part of our continued growth, we are hiring PhD Graduates into our Analytics community who will start their career with 15 months rotating across 3 key areas of the organization. You will have...
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Principal Biostatistician
1 month ago
London, United Kingdom Advanced Group Full timeA Principal Biostatistician is responsible for directing assigned projects and providing statistical support for clinical trials. This includes generating randomization schedules, participating in protocol and SAP development, preparing and reviewing programming specifications used in creating derived datasets, tables, listings, and figures, and reviewing...
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Principal Biostatistician
1 month ago
London, United Kingdom Planet Pharma Full timeThe primary purpose of the Principal Statistician is to act independently as Study Statistician for complex work in an established area within clinical studies. This position may also act as Global Statistical Lead for an early or back up asset or as a Methodology expert validating the execution of complex techniques.This role will be dedicated to the...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Clinical Development Director Oncology
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timePLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within GSK's Oncology Clinical Development organization is for you. The Senior Medical Director Oncology...
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Senior Medical Director
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timeSite Name: UK – London – New Oxford Street, UK - Hertfordshire - Stevenage Posted Date: Jul 19 2024 PLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity...
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Senior Medical Director
3 weeks ago
London, United Kingdom GlaxoSmithKline Full timeSite Name: UK – London – New Oxford Street, UK - Hertfordshire - Stevenage Posted Date: Jul 19 2024 PLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time . Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity...
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Senior Medical Director
1 month ago
London, United Kingdom GlaxoSmithKline Full timeSite Name: UK – London – New Oxford Street, UK - Hertfordshire - StevenagePosted Date: Jul 19 2024PLEASE NOTE CLOSING DATE: Monday, August 5th, 2024 at midnight US time.Are you a physician scientist keen to progress your oncology pharma career in the innovative and exciting field of ADCs? If so, this Senior Medical Director career opportunity within...
Principal Biostatistician
2 months ago
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on .
Principal Biostatistician:
Roles and Responsibilities
Can create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams. Can develop SAPs and iSAPs text and shells with no supervision. Can review or develop ADAM specifications; can work with programmers and junior statisticians to resolve comments. High technical level, Subject Matter Expert in biostatistics; willing to guide others in a variety of biostatistical techniques. Has the ability to apply drug development knowledge during production of complex statistical analyses. Can perform sample size calculations for a variety of scenarios and study designs. Can provide statistical consulting support to sponsors re study design and sample size calculations. Leads complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. Is familiar with and stays current with the latest industry practices and updated regulatory guidelines. Understands the various tools that we work with and able to use them correctly (for SCM: checks in/out; use of external SharePoint). Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician. Has high level knowledge of drug development as it pertains to biostatistics. Produces and presents external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction. Write blogs and/or white papers for posting on the company website Review or create the statistical section(s) of a Sponsor’s protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study. High proficiency with MS Office applications Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation/management. Prepare and review statistical methods and results sections for the CSR independently in collaboration with in-house medical writers.Requirements
Masters in Biostatistics, Statistics discipline or related field, or related experience, PhD preferred. Minimum of 7 years’ experience in Biostatistics, Statistics or similar field required. Expert knowledge of scientific principles and concepts. Reputation as emerging leader in field with sustained performance and accomplishment. Proficiency with MS Office applications. Hands-on experience with clinical trial and pharmaceutical development preferred. Good communication skills and willingness to work with others to clearly understand needs and solve problems. Excellent problem-solving skills. Good organizational and communication skills. Familiarity with current ISO 9001 and ISO 27001 standards preferred. Familiarity with 21 CFR Part 11, FDA, and GCP requirements. Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.