- Merck & Co. (Rahway, NJ)
- …interest to the company. The RMSD provides research support to our Investigator -Sponsored and Company-Sponsored Trials to enhance the understanding of the scientific ... patient enrollment and retention efforts for a given study or address Investigator questions. RMSDs also respond to scientific questions from SLs, including… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. SUMMARYProvide support to the Global and Regional Quality Leads, External Partner Quality Leads, and Business Partner ... Quality Leads based on assigned programs and in close collaboration with R&D Quality team members to ensure that the organization is in a perpetual state of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leadership:Has primary accountability for operational study level time, cost and quality deliverables.Lead the development of the clinical study plan including ... study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, Operations Program Lead, and Sr.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... clinical studies/programs on time with a focus on budget, compliance and quality . Leads strong and effective communication to global and local stakeholders to… more
- Insmed Incorporated (San Diego, CA)
- …the clinical development strategy and clinical protocols and delivering high quality clinical programs, from first-in-human trials, through to full development.Serve ... of clinical operations, toxicology, regulatory affairs, commercial, pharmacovigilance, clinical quality , and biostatistics.Provide medical leadership for key areas of… more
- Merck & Co. (Rahway, NJ)
- …. Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address clinical supply related topics ... well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. Support the collection of clinical suppl y… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Writing is a key role responsible for producing scientifically accurate, high- quality clinical regulatory documents while adhering to regulatory guidelines. This ... documents include, but are not limited to, clinical study reports, investigator brochures, regulatory briefing documents, and clinical and clinical pharmacology… more
- Tris Pharma (Monmouth Junction, NJ)
- …disseminate scientific information and report Adverse Events (AEs) and Product Quality Complaints (PQCs)Collaborates with VP/Medical Affairs to ascertain and secure ... Medical Affairs strategiesCoordinates MSL support for clinical activities and investigator -initiated research (IIR); Coordinates MSL support for medical information,… more
- Taiho Oncology (Philadelphia, PA)
- …product(s) and compounds to ensure awareness and understanding. Provides high quality scientific information to healthcare professionals (HCPs) Serve as a conduit ... In collaboration with Medical Affairs personnel support data generation Investigator -Initiated Trials (IITs) and HCP initiated projects. Facilitate the review… more
- Richmond Community Services (Mount Kisco, NY)
- … Quality Specialist/ Investigator for our growing population. The Quality Investigator coordinates and maintains all notification, investigation, and ... to ensure compliance with applicable codes and regulations and to enhance the quality of care of all individuals. Must have previous investigative experience to be… more
