- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of employee and/or contractor-based staff/analysts to support the overall delivery of a clinical trial diversity and patient access strategy. Qualifications: ... mechanisms at the study team and clinical trial site level to proactively monitor diversity ...experience required Experience Qualifications.7 or More Years 7 years clinical operations experience in trial diversity… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …employer including veterans and people with disabilities. Summary The Associate Director , Clinical Data Standards, is responsible for the development, ... pipeline.Proactively identify Data Standards gaps and resolve issues related to clinical data standards development throughout the trial lifecycle.Standardize… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …investigators is expected. The CS Group Lead will also ensure the writing of high-quality clinical trial protocols, review of clinical data and Clinical ... Innovation 110 Years and Counting! Company is committed to diversity and inclusion. We are an equal opportunity employer...Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical… more
- Bristol Myers Squibb (Summit, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data towards development + Serving as principal functional ... or industry setting including education where applicable + Extensive experience in clinical trial design and execution, biomarker development, and development… more
- Bristol Myers Squibb (Summit, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... in their personal lives. Read more: careers.bms.com/working-with-us . The Director will be the clinical lead to...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …employer including veterans and people with disabilities. **Summary** The Associate Director , Clinical Data Standards, is responsible for the development, ... + Proactively identify Data Standards gaps and resolve issues related to clinical data standards development throughout the trial lifecycle. + Standardize… more
- Bristol Myers Squibb (Madison, NJ)
- …on major markets and key assets; adjust communications plans in accordance with clinical trial results/milestones and changes in the market healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …rives the development and implementation of innovative strategies and technologies for clinical trial programming. A ssociate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- AbbVie (Newark, NJ)
- …analysis plans and reports + Leads integration of COA measurement strategy into clinical development programs through clinical trial program support (eg, ... / knowledge of the pharmaceutical industry (knowledge of regulatory/compliance frameworks) and clinical trial design + Knowledge of global regulatory & HTA… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & ... the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses &… more
- AbbVie (Florham Park, NJ)
- …Completion of residency and/or fellowship is preferred. + Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or ... strategy. Field experience preferred but not required. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements… more
- Bristol Myers Squibb (New York, NY)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge of ... in their geography + Ensures FM team's execution of clinical trial support activities (as per established...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Bristol Myers Squibb (Madison, NJ)
- …Global Data Management (GDM) **Functional Area Description** GDM is responsible for clinical trial data acquisition, data management and review, and medical ... + Expert understanding of the drug development process and clinical trial execution. + Expert knowledge of...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- The Mount Sinai Health System (New York, NY)
- …* Supportive and experienced clinical staff * State of the art clinical trial unit, clinical and translational research environment and affiliated ... Icahn School of Medicine at Mount Sinai seeks a Director for its Skin of Color Center in Manhattan!**...with a strong academic record of accomplishments and/or academic, clinical and research productivity, impressive publications and a deep… more
- J&J Family of Companies (Raritan, NJ)
- …to key regulatory or clinical documents including: + Risk management plans + Clinical Trial , EAP and IIS Protocols + Informed Consent Forms (ICF), including ... Director , Medical Safety Officer, Solid Tumor Oncology -...+ Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring… more
- AbbVie (Florham Park, NJ)
- …submitted to the regulatory authorities. + Participate in the design and execution of clinical trial safety, product safety and risk management plans. May also ... + Minimum of 2 years of medical affairs and/or clinical trial or clinical practice...driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ… more
- Bristol Myers Squibb (Madison, NJ)
- …apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, ... opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity . Take your career farther than you thought possible. Bristol Myers Squibb… more
- AbbVie (Madison, NJ)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director , Medical Affairs & Health Technology Assessment (MA&HTA) Statistics leads and ... or more assigned therapeutic indication areas. A visible and collaborative role, the Director works in partnership with Medical Affairs, Market Access & Pricing and… more
- Bristol Myers Squibb (Madison, NJ)
- …apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, ... opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity . Take your career farther than you thought possible. Bristol Myers Squibb… more
- AbbVie (Florham Park, NJ)
- …experience in the pharmaceutical industry is preferred. + Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements ... sit in our Lake County, IL or Madison, NJ offices. The Scientific Director for US Medical Affairs in CNS/Psychiatry provides specialist medical and scientific… more
