• Highly Distinguished/ Distinguished Research…

    Boehringer Ingelheim (Ridgefield, CT)
    …investigative study work packages, developing study designs and their placement (internal, CRO ) and execution * Capable of independently serving as broad subject ... author) and at least 10 years of experience in pharmaceutical R&D with track record of independent research **Highly...author) and at least 15 years of experience in pharmaceutical R&D with track record of independent research **Eligibility… more
    Boehringer Ingelheim (08/30/25)
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  • Senior Research Advisor, Analytical Chemistry…

    Lilly (Indianapolis, IN)
    …engineers while offering access to world-class capabilities for pharmaceutical development. **Responsibilities:** + Develop analytical methods, justify ... performance characteristics. + Collaborate with project teams to develop robust control strategies for drug substances, drug products, and/or drug product… more
    Lilly (08/30/25)
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  • Executive Medical Director, US Medical Affairs…

    Amgen (Thousand Oaks, CA)
    …more years of Medical Affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO ) that includes collaborations with integrated delivery ... a balanced, realistic understanding of issues + Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but… more
    Amgen (08/28/25)
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  • Sr. Director / General Manager, Clinical Trials…

    ThermoFisher Scientific (Mount Prospect, IL)
    …goals. **Location/Division Specific Information** Clinical Trials Division (CTD) partners with pharmaceutical and biotech customers around the world to ensure the ... Well-developed communication and customer skills Preferred Qualifications: + MBA + Pharmaceutical clinical or commercial supply experience + Experience running a… more
    ThermoFisher Scientific (08/28/25)
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  • Research Enablement Lead, Director

    Takeda Pharmaceuticals (Boston, MA)
    …Director in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... global communications, including coordination of information between TBOS and TSHO + ** CRO Management Support for In Vitro Pharmacology** + Ensure IVP group operates… more
    Takeda Pharmaceuticals (08/08/25)
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  • Director, Business Development (Remote)

    WCG Clinical (Cary, NC)
    …relationships with medical and clinical operations decision-makers at pharmaceutical , biopharma, biotech, and medical device companies. **ESSENTIAL ... and services via a consultative selling approach within assigned global bio pharm/ CRO clients + Coordinates with leaders and SMEs across the organization to… more
    WCG Clinical (08/08/25)
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  • Senior Director, Scientific

    AbbVie (Chicago, IL)
    …is a plus *Typically 10+ years of clinical development experience in the pharmaceutical industry, CRO , academia or other health-related consulting company plus ... relevant therapeutic specialty. Clinical research experience strongly recommended; within pharmaceutical industry preferred *Must perform at times in previously… more
    AbbVie (07/16/25)
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  • Senior Medical Director, Clinical Science,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …equivalent plus 7 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical ... team on a high priority molecule. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
    Takeda Pharmaceuticals (07/10/25)
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  • Research Analyst I - In Vitro

    Charles River Laboratories (Shrewsbury, MA)
    …**About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
    Charles River Laboratories (09/25/25)
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  • FSP Principal Medical Writer

    ThermoFisher Scientific (Wilmington, NC)
    …complex medical writing projects required Experience working in the pharmaceutical / CRO industry preferred Submissions document experience advantageous Additional ... qualifications in medical writing (AMWA; EMWA; RAC) advantageous **Knowledge, Skills, and Abilities:** + Expert knowledge of global, regional, national, and other document development guidelines + Expert knowledge in one or more specialty areas such as… more
    ThermoFisher Scientific (09/25/25)
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