- 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
- J&J Family of Companies (Titusville, NJ)
- …Jersey, United States of America **Job Description:** Johnson & Johnson is recruiting for a Senior Specialist , QA Clinical Auditor to be located anywhere in ... + A minimum of 5 years of related work experience in auditing, clinical trial operations, or a related space + Knowledge of the drug development process,… 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
- 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
- Bausch + Lomb (Trenton, NJ)
- …ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + Support ... regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor… 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