- Organon & Co. (Jersey City, NJ)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
- Merck (Rahway, NJ)
- … **Primary activities include, but are not limited to:** - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and...prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible… more
- Merck (Rahway, NJ)
- …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must ... to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely...prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. + Works… more
- Mount Sinai Health System (New York, NY)
- …and distribution of funding opportunities packets, calendars and special alerts. + Contracts Specialist Negotiate clinical trial agreements and amendments on ... the integration of the latest discoveries in the lab and innovations in clinical care into patient-centric care models in the safest, and most compassionate way… more
- Merck (Rahway, NJ)
- …viral dynamics, model-based meta-analysis, and other model-based analyses + Perform clinical trial simulations to inform dose selection and go/no-go ... **Job Description** Senior Specialists in the Infectious Disease and Vaccines...global regulatory expectations of drug and vaccine development, including clinical trial design, clinical pharmacology,… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …Oversee the internal packaging and labeling production orders in accordance with the clinical trial design and all relevant regulatory requirements for assigned ... effective management of assigned projects. Manages multiple projects. Liaise with responsible Trial Supply Managers on aspects of clinical supplies packaging and… more
- Actalent (Hackensack, NJ)
- …of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in clinical ... representative in communications with sponsors and IRB. + Maintain accurate records on clinical trial protocols in the clinical trial management system.… more
- Actalent (Hackensack, NJ)
- …+ Minimum of 2 years in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years of related experience in clinical ... and Radiology Department. + Maintain accurate documentation and records related to clinical trial activities. + Support workflow development and process… more
- Hackensack Meridian Health (Hackensack, NJ)
- …of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education, Knowledge, Skills and… more
- Sanofi Group (Morristown, NJ)
- …T1D screening events per global standards + Prioritize Identification of suitable clinical trial and registry sites and provide comprehensive support throughout ... **Job Title:** T1D Immunology Senior Medical Science Liaison, NYC, Long Island **Location:**...meetings. + Continuous engagement in key accounts to create clinical value and demonstrated impact through exceptional/innovative field medical… more
- Sanofi Group (Morristown, NJ)
- …progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team (CTT) and Project Team. This is a position for a ... senior medical writer who has an extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as… more