- Merck (Providence, RI)
- **Job Description** With support of Sr CRA ( Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager throughout all ... of site relationships through all phases of the trial . + Performs clinical study site management/monitoring activities in compliance with ICH-GCP,… more
- Merck (Providence, RI)
- …and ensures continuity of site relationships through all phases of the trial . + Performs clinical study site management/monitoring activities in ... externally. Acts as primary site contact and site manager throughout all phases of a clinical... site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.… more
- Merck (Providence, RI)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Merck (Providence, RI)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas....seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
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