- 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
- 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
- ThermoFisher Scientific (Bohemia, NY)
- …and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times. **How will you make an impact?** ... Specialist is responsible for the compliance of the Clinical Label Services Quality Management System (QMS), which includes...metrics related to CLS Quality compliance and present to Senior management on a scheduled basis. + Support site… 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
- Boehringer Ingelheim (Ridgefield, CT)
- …under their responsibility as delegated by TA HoEM. + Review and approve final Clinical Trial Reports, Clinical Trial Protocols, scientific publications ... + Ensures the review of the Master Plans, related Clinical Development plans and Clinical Trial...years (combination of hospital, academic and industry experience),inclusive of senior leadership role/s; Clinical / pharma experience… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Lead ensures the definition of reasonable PoCP criteria, state of the art clinical trial designs, feasibility of PoCP strategies as well as realistic ... accredited institution with profound experience in the field of Clinical Development, TMCP and specialist in the... clinical development, exploratory clinical , and clinical pharmacology in the pharmaceutical industry. + Senior… more