- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... team and collaborate with the core and extended team to ensure robust CRO oversight including 3rd party vendors to achieve study milestones and deliverables… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... process improvements and support of additional guidance, tools, etc. as necessary. CRO /Vendor and Quality OversightAccountable to ensure proper oversight of CROs… more
- Insmed Incorporated (NJ)
- …considered relevant includes clinical or basic research in a Pharmaceutical company, Academic Research Organization (ARO) or Contract Research Organization ... ( CRO ).Experience in rare disease and/or orphan indications is preferred.Knowledgeable...and set direction in related areas such as compliance, CRO management, risk management, etc.Ability to prioritize and manage… more
- Eisai, Inc (NJ)
- …10 years relevant work experienceBA/MS in relevant fieldExperience in pharmaceutical setting requiredProven experience managing CRO /vendor relationships and ... and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... supporting Clinical R&D and PH.1 to PH. IV outsourced services (eg, CRO , Biomarker, CDx, Clinical Supplies, central labs); Must have strong problem-solving skills… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... the datasets created by other programmers or by the CRO . Develop code to verify the accuracy of the...and Listings created by other programmers or by the CRO . Answer questions from the CRO regarding… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... strategic sourcing, vendor governance, and clinical operations within a pharmaceutical environment. Strong communication skills, executive presence, and proficiency… more
- Formation Bio (New York, NY)
- …capabilities, and a strong regulatory and industry knowledge base in pharmaceutical sciences or engineering to drive successful drug product development and ... pharmacology and project management to support short and long term program objectives. CRO and CDMO Management: Oversee and manage drug product vendors, for both… more
- Aequor (South San Francisco, CA)
- …include academic research, public health studies, data analysis, or work within pharma/ CRO environments. Knowledge and experience in How many years of experience you ... in designing, conducting, analyzing and interpreting epidemiological studies (includes healthcare/ pharmaceutical HTA related experience) and/or Real World Data (RWD)… more
- Eisai, Inc (Exton, PA)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... and techniquesNegotiate service contracts with external providers. Assess and document CMO/ CRO analytical proficiencies and readiness to perform various types of… more
- Genmab (NJ)
- …in clinical drug development, including significant experience in feasibility within pharmaceutical , biotech, or CRO settings.Proven leadership of complex, ... global feasibility initiatives and ability to influence clinical development strategy.Track record of cross-functional leadership in matrixed environments.Experience mentoring or managing colleagues, even in an informal or project-based capacity.Proficiency in… more
- Insmed Incorporated (NJ)
- …Minimum of 8 years of clinical/statistical programming experience in a biotech, pharmaceutical , or CRO setting required Extensive knowledge of SAS software ... (ie, Base, Stat, Graph components) and general computing techniques in addition to knowledge of R or other statistical software packages Significant knowledge of the drug development process, clinical trial methodology, and relevant regulatory requirements for… more
- Genmab (NJ)
- …Science, Life Sciences preferred At least 6-8 years relevant experience in a pharmaceutical , biotech, CRO or Regulatory Agency Proficient in SAS programming, 6-8 ... matter expert on data standards, reporting and analysis standards, change control management and related tools/applications Creates quality control processes,… more
- Unknown (Portland, OR)
- …a minimum of 8 years' experience in drug safety or pharmacovigilance within the pharmaceutical , biotech, CRO , or regulatory agency. The role requires a strong ... knowledge of US and EU drug safety regulations, CIOMS, and ICH guidelines, as well as experience in managing medical professionals and PV scientists. Proficiency in medical review of safety data, including ICSRs and aggregate reports, is essential. The ideal… more
- United Therapeutics (Research Triangle Park, NC)
- …years of related clinical study management or project management experience in CRO / pharmaceutical operations and development + Master's degree in related field ... of related clinical study management or project management experience in CRO / pharmaceutical operations and development + Education and Experience requirements… more
- Vitalief (Phoenix, AZ)
- …a highly skilled and motivated Clinical Research Associate (CRA) to support our pharmaceutical client, based in the Phoenix, AZ area, in executing multiple clinical ... dermatologic conditions, and metabolic disorders. This hybrid role combines CRO oversight responsibilities with hands-on monitoring activities, offering the… more
- Charles River Laboratories (Wilmington, MA)
- …animal models or preclinical research services. * Deep understanding of the pharmaceutical and CRO landscape, particularly in preclinical development. * ... to lead sales efforts for our non-human primate (NHP) portfolio, targeting pharmaceutical companies and contract research organizations (CROs). This role is critical… more
- Taiho Oncology (Princeton, NJ)
- …years of relevant clinical trial management and leadership experience in the pharmaceutical , biotechnology, CRO and/or healthcare industry. + Has demonstrated ... internal cross-functional study teams and managing, contract research organization ( CRO ) personnel and other study vendors. Performs assigned responsibilities to… more
- Rhythm Pharmaceuticals (Boston, MA)
- …BA/BS degree, advanced degree preferred + 5+ years of relevant experience within a CRO , pharmaceutical , and/or biotech company + Experience working on Phase I - ... + Manage integrations of all clinical study activities leveraging internal and CRO resources, expertise and knowledge + Provide trial cost estimates and timelines… more
- Takeda Pharmaceuticals (Boston, MA)
- …feasibility, and trial optimization with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor. + Direct ... reporting to the Director, Feasibility. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led… more
