- Leads statistical programming activities across a Therapeutic Area and related oversight activities ensuring quality and timeliness
- Leads the recruitment and retention strategies for Statistical Programming for CT Stats Programming, including CMC programming in partnership / collaboration with Statistical Programming LT, Programming Leads, HR and Talent Acquisition teams.
- Leads statistical programming Therapeutic Area level strategies in partnership with the VP of Biostatistics
- Sets tasks and prioritization across the Therapeutic area
- Successfully engages cross functionally to progress tasks with proven influencing skills
- Leads process improvement initiatives, including identification of areas of improvement
- Existing influential internal and external presence on varied statistical programming topics
- Provides comprehensive programming leadership and support to complex clinical project teams and vendors, including deployment of programming strategies, standards, specifications and programmed analysis to comply with regulatory requirements, SOPs and work practices
- Provides guidance on developing and implementing innovative strategies and technologies for clinical trial programming
- Member of Statistical Programming Leadership Team in sharing and building up the line function vision
- MS with ~10+ years of industry related experience.
- BS with ~12+ years of industry related experience.
- Proven track record of leading business process transformations and organizational culture change as well as driving programming expertise on programs with complex business deliverables
- Proven track record of attracting and retaining talent
- Operational experience in pharmaceutical drug development with significant direct exposure to clinical development
- Health care business acumen with a comprehensive understanding of the pharmaceutical industry
- Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical concepts, and medical terminology used in the analysis and submission of clinical data
- Member of industry organizations or presented at Congresses/Conferences
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Commercial Training Associate Director
1 week ago
Park Street People London, United Kingdom**A global biotechnology company who are a market leader in their therapeutic area are looking for a Commercial Training Associate Director to join their team.** · Covering international training programmes, you will be able to combine strategy creation/planning with operational ...
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Summer 2023 Intern
18 hours ago
Prescient Healthcare Group London, United Kingdom**Summer 2023 Intern** · **Application Deadline Friday 24**th** February** · **About You** · Have you decided biopharma consulting is for you? Are you looking to leverage your life sciences qualifications and academic experience into a business focused career? Prescient is lookin ...
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Clinical Study Specialist
3 weeks ago
Regeneron Pharmaceuticals Inc. Uxbridge, United KingdomThe Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from th ...
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Senior Quality Assurance Manager
6 days ago
Xcene Research england, United KingdomCompany Description · Xcene Research is a pioneering Contract Research Organization (CRO) located in Lagos, Nigeria, specializing in the management, execution, and analysis of clinical trials ranging from Phase I through Phase IV, including small to complex multinational trials. ...
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Senior Cra
3 weeks ago
Fortrea Maidenhead, United KingdomAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and techn ...
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Senior Cra
2 weeks ago
Fortrea - Organic Maidenhead, United KingdomOur Clinical Operations department in the UK is looking for 4 Senior CRAs to work mainly on complex Oncology trials. You can be based anywhere in the UK but we do need previous UK monitoring experience. · The role in summary: · - National monitoring across the UK · - Studies will ...
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Bristol Myers Squibb United KingdomWorking with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production li ...
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Manager/Quality Manager
2 weeks ago
Xcene Research United KingdomXcene Research is a pioneering Contract Research Organization (CRO) located in Lagos, Nigeria, specializing in the management, execution, and analysis of clinical trials ranging from Phase I through Phase IV, including small to complex multinational trials. We offer services in v ...
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Senior Quality Assurance Manager
1 week ago
Xcene Research London, United KingdomCompany Description · Xcene Research is a pioneering Contract Research Organization (CRO) located in Lagos, Nigeria, specializing in the management, execution, and analysis of clinical trials ranging from Phase I through Phase IV, including small to complex multinational trials. ...
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DirectorDirector
1 week ago
OPEN Health Group London, United KingdomReports to the EVP, Medical & Scientific Services · The Scientific Director will have the skills and ability to lead multiple projects for multiple clients simultaneously. They will serve as the medical expert for the teams they support, understanding the therapeutic landscape a ...
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Team Lead Development
5 days ago
ClinChoice Inc. United KingdomAre you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? ClinChoice is searching for a Statistical Programming, TA Standards and Leader -Oncology to join one of our clients. ...
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Senior Clinical Studies and Project Manager
2 weeks ago
Barrington James London, United KingdomOur company is a lead CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our European locations. Clinical Trial Managers with expertise in Oncology/Hematology, Cardiovascular, In ...
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Scientific Director
1 week ago
OPEN Health Group London, United KingdomReports to the EVP, Medical & Scientific Services · Job Summary · The Scientific Director will have the skills and ability to lead multiple projects for multiple clients simultaneously. They will serve as the medical expert for the teams they support, understanding the therapeu ...
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Scientific Director
4 weeks ago
Lockwood Group United KingdomAbout Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies to address their objectives through medical communications. Our clients count on us to challenge their assum ...
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Manager/Quality Manager
1 week ago
Xcene Research England, United KingdomCompany Description Xcene Research is a pioneering Contract Research Organization (CRO) located in Lagos, Nigeria, specializing in the management, execution, and analysis of clinical trials ranging from Phase I through Phase IV, including small to complex multinational trials. We ...
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Senior Clinical Projects Manager
2 weeks ago
Barrington James United KingdomOur company is a Pharmaceutical Company and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our European locations. Clinical Trial Managers with expertise in Oncology/Hematology, Cardiovascular, Infectious ...
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Senior Quality Assurance Manager
1 week ago
Xcene Research England, United KingdomCompany Description Xcene Research is a pioneering Contract Research Organization (CRO) located in Lagos, Nigeria, specializing in the management, execution, and analysis of clinical trials ranging from Phase I through Phase IV, including small to complex multinational trials. We ...
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ClinChoice Inc. United KingdomAre you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds.... · ClinChoice is searching for a Statistical Programming, TA Standard ...
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Nurse Refresher
5 days ago
Baltimore Partnership United KingdomContinuing Education Workforce Certificate · Nurses play a critical role in a wide variety of healthcare settings ranging from acute care hospitals, physician's offices, urgent care centers, ambulatory care facilities, long-term care centers, to school nurse's offices. A registe ...
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Senior Clinical Project Manager
1 week ago
Barrington James London, United KingdomOur company is a lead CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our European locations. Clinical Trial Managers with expertise in Oncology/Hematology, Cardiovascular, In ...
Sr. Director, Head Stats Programming Hematology - United Kingdom - Bristol Myers Squibb
Description
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. #J-18808-Ljbffr
