- Ascendis Pharma (Princeton, NJ)
- …are a dynamic workplace for employees to grow and develop their skills. The Senior Manager , Clinical Trial Supplies (CTS), Oncology will work as an integral ... CTS Oncology team, managing all aspects of Investigational Medicinal Products (IMP), Clinical Trial Supplies, Comparators and ancillary products used in Ascendis… more
- Bristol Myers Squibb (Princeton, NJ)
- …of concept, full development and/or across marketed products. + Experience in conducting global clinical trial programs across major worldwide markets, ... personal lives. Read more: careers.bms.com/working-with-us . Position Title: Executive Director, Global Trial Management, TA Head Immunology/CV Functional Area… more
- Bristol Myers Squibb (Princeton, NJ)
- …portfolio. + Collaborate with the TA Medical Lead, CTL, Clinical Scientist (CS), and Global Trial Manager (GTM) for the development of the Medical study ... Generation (MEG) Lead - Cell Therapy (CT) role in Global Medical Affairs manages the evidence generation for the...MD preferred, but not required, plus 2-3 years of clinical trial experience, either in industry or… more
- Actalent (Princeton, NJ)
- … Budget Development will serve as a subject matter expert in the development of global clinical trial budgets. The role will frequently collaborate with R&D, ... protocols (protocol complexity, underrepresented participant populations, etc.). + Independently create global and country-specific clinical trial budget… more
- Merck (Trenton, NJ)
- …Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). + Responsible for project management of the ... research knowledge is required. + Strong understanding of clinical trial planning, management and metrics is...goals, purpose and mission of our Company Research Labs, Global Clinical Development (GCD) and GCTO. +… more
- Novo Nordisk (Plainsboro, NJ)
- … Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex ... department, (subset of) NACD and/or as part of a global team and as aligned to a business case,...trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical… more
- Merck (Trenton, NJ)
- …activity. + Develop, update, and maintain GCP inspection procedures and guidelines within Global Clinical Trial Operations (GCTO). + Contribute to the ... and Head of Clinical Quality Operations, the Clinical Quality Operations Manager (CQOM) is accountable...oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic… more
- Bristol Myers Squibb (Princeton, NJ)
- …experience in BMS clinical trials. Will serve as a key member of clinical trial teams, partnering with various internal and external stakeholders to support, ... in a variety of indications to drive and accelerate clinical trial recruitment for BMS. **Key Responsibilities**...Administration or equivalent. Advanced degree a plus. + **Sr. Manager :** Clinical development experience of **3 to… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …science preferred, + 4+ years in Clinical Operations, Data Analytics, global feasibility, and trial optimization with evidence of increasing responsibility ... of disease, access to targeted patient population, drug landscape, historical/current clinical trial landscape) to influence and inform protocol development,… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …+ 6+ years of experience in Clinical Operations, Data Analytics, global feasibility, and trial optimization with evidence of increasing responsibility within ... of disease, access to targeted patient population, drug landscape, historical/current clinical trial landscape) to influence and inform protocol development,… more
- Bristol Myers Squibb (Trenton, NJ)
- …writing and organizational skills + Ability to: + Learn regulatory requirements & clinical trial design, data analysis and interpretation, + Work successfully ... and advanced statistical methods is preferred. + Good understanding of regulatory requirements & clinical trial design is preferred. _If you come across a role… more
- Bristol Myers Squibb (Princeton, NJ)
- …writing and organizational skills + Ability to: - learn regulatory requirements & clinical trial design, data analysis and interpretation, - work successfully ... us and make a difference. Position Summary The Senior Manager of Biostatistics is a member of cross-functional development...is preferred. + Good understanding of regulatory requirements & clinical trial design is preferred. **Why You… more
- Bristol Myers Squibb (Trenton, NJ)
- …Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical ... of Medical Communications within WWM CV & EB, of Global Medical Affairs and is responsible for the planning...in WWM CV & EB. **Key Responsibilities** The Senior Manager of Medical Communications is accountable for the following:… more
- Bristol Myers Squibb (Trenton, NJ)
- …the development and execution of statistical aspects for BMS medical sponsored clinical trials, including contribution to study trial design, analysis planning, ... us and make a difference. Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to...study results presentation and interpretation, clinical study report authoring and publications. + Provides statistical… more
- Novo Nordisk (Plainsboro, NJ)
- …preferred + A minimum of eight (8) years of progressively responsible clinical development/ trial experience within a pharmaceutical, biotechnology, or CRO ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at...above within CMR Training & Knowledge Management. Collaborates with global and CMR leaders and stakeholders to develop comprehensive… more
- Bristol Myers Squibb (Trenton, NJ)
- …BLA, MAA) + Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements + ... . Managers of Statistical programming provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and… more
- Bristol Myers Squibb (Trenton, NJ)
- …BLA, MAA). + Knowledge of the drug development process, clinical trial methodology, statistics, and familiarity with global regulatory requirements. + ... Managers of Statistical programming provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and… more
- Bristol Myers Squibb (Trenton, NJ)
- …towards industry experience + Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical ... Senior Managers of Statistical Programming provide comprehensive programming expertise to clinical project teams to lead statistical programming teams and support… more
- Taiho Oncology (Princeton, NJ)
- …of technical issues, eg, during process development/validation, manufacturing, and release of clinical trial material. + Contributes to initiatives to improve ... Sr. Manager , Analytical Development Princeton, NJ, USA Req #362...we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.… more
- Merck (Trenton, NJ)
- …FDA, CFIA and USDA regulatory policies. The position will require developing trial protocols, monitoring and summarizing clinical and marketing support trials ... trials and product development for all our company products. Perform field trial evaluation of newly license products to offer technical support information for… more