- 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 (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 (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
- Rubrik (Trenton, NJ)
- …environment. **What you'll do:** + Lead and act as the primary investigator during incident response (IR) activities, leveraging expertise in enterprise forensics. ... against on the basis of disability. Rubrik provides equal employment opportunities ( EEO ) to all employees and applicants for employment without regard to race,… more
- Bristol Myers Squibb (Madison, NJ)
- …Evidence Generation to ensure support of BMS-sponsored clinical trials and investigator -sponsored research (ISRs) within the US portfolio. + Facilitate scientific ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
- Bristol Myers Squibb (Princeton, NJ)
- …with Medical Evidence Generation (MEG) to oversee the execution of the Investigator Sponsored Research (ISR) programs from concept through full execution, including ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
- Bristol Myers Squibb (Princeton, NJ)
- …of clinical study protocols and related documents (eg, Informed Consent Forms, Investigator Brochures). + Support the design and implementation of clinical trials in ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
- Bristol Myers Squibb (Madison, NJ)
- …Affairs Sponsored studies [MAST], Clinical Research Collaborations [CRC], and investigator -sponsored studies [ISR]) and provides leadership for the cross-functional ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
- Bristol Myers Squibb (Madison, NJ)
- …Develop site and CRA training materials and present these at SIVs and Investigator meetings + Review clinical narratives + Monitor clinical data for specific trends ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
- Bristol Myers Squibb (Princeton, NJ)
- …utilization by clinical sites. + Educate clinical site personnel through in-services, investigator meetings and clinical site initiations or follow-up visits on the ... process, direct your inquiries to ###@bms.com . Visit careers.bms.com/ (https://careers.bms.com/ eeo -accessibility) eeo -accessibility to access our complete Equal… more
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