• Organon & Co. (Jersey City, NJ)
    …2.5 and labeling for regulatory submissions, contribute the authoring of Investigator Brochures, IND subsections, briefing books, submission modules, responses to ... pharmacology components of TMED study protocols, clinical study reports, Investigator Brochures, briefing books, IND subsections, submission modules and other… more
    DirectEmployers Association (10/02/25)
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  • Parexel (Trenton, NJ)
    …with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and ... preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is… more
    DirectEmployers Association (10/10/25)
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  • Organon & Co. (Jersey City, NJ)
    …modules for regulatory submissions, contribute the authoring and review of Investigator Brochures, INDs, briefing books and other regulatory documents, as ... under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement OFCCP Pay Transparency Rule Organon is an Equal Opportunity… more
    DirectEmployers Association (10/24/25)
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  • Parexel (Trenton, NJ)
    …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... in a wide range of disciplines Education: - BA/BS or higher \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive… more
    DirectEmployers Association (10/10/25)
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  • Parexel (Trenton, NJ)
    …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... documents **Education:** + BA/BS, Advanced degree preferred \#LI-LO1 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants… more
    DirectEmployers Association (10/10/25)
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  • Senior Manager, Cell Therapy Network Lead…

    Bristol Myers Squibb (Summit, NJ)
    …Read more: careers.bms.com/working-with-us . **Position Summary** Cell Therapy Network Lead investigator will support the commercial and late stage clinical cell ... for complex trend investigations stemming from deviations and SAEs. The lead investigator will assemble and lead cross functional matrix teams necessary to close… more
    Bristol Myers Squibb (09/19/25)
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  • Senior Medical Science Liaison - Biopharma…

    Sumitomo Pharma (Jersey City, NJ)
    …drug/brand development. + Identify, initiate, coordinate, evaluate and monitor investigator -sponsored studies intended to support the clinical and scientific ... products. + Help develop and manage timelines of publication plans of investigator -sponsored studies. + Assist in the identification, evaluation, and engagement of… more
    Sumitomo Pharma (10/22/25)
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  • Sr. Medical Director, Clinical Development (GU…

    Bristol Myers Squibb (Princeton, NJ)
    …to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and ... regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators + Execute and deploy drug… more
    Bristol Myers Squibb (10/11/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Trenton, NJ)
    …CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute to content as needed… more
    Sumitomo Pharma (10/11/25)
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  • Senior Medical Director, Clinical Research…

    Sumitomo Pharma (Trenton, NJ)
    …writing of clinical study reports + Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final reports in compliance ... globally + Contributes to the development of presentation materials for investigator meetings, health authority meetings, scientific advisory board meetings, and… more
    Sumitomo Pharma (09/27/25)
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