- Parexel (Albany, NY)
- The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management and monitoring,...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Pfizer (New York, NY)
- …delivery unit within the Clinical Development &Operations (CD&O) organization, the Senior Associate , eCOA Manager, Clinical Data Collection Strategies is ... this role, you will: + As part of the Clinical Data and Information Sciences (CDIS) group, an integral...process + The candidate will have significant eCOA and/or trial management experience with technical expertise in eCOA. +… more
- Grifols Shared Services North America, Inc (New York, NY)
- …success in the MSL role. Consideration will be given to applicants with senior -level MSL expertise, based on experience and credentials. **This position is a remote ... cross-functional colleagues by support at medical conventions, advisory boards, clinical data presentations, scientific intelligence, promotional speaker training, company… more
- Parexel (Albany, NY)
- **Job Purpose:** The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study… more
- Pfizer (Pearl River, NY)
- …country feasibility. **Support study team** + With supervision of medical monitor (Director/ Sr Director) provides clinical input to protocol/study team for ... and reporting. + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare… more
- Otsuka America Pharmaceutical Inc. (Albany, NY)
- **Job Summary** Under the direction of the Director/ Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the ... communication of any variances in budget forecast to the Director/ Associate Director. * Establish communication flow with CRO and...(s), as assigned. * Participates in ongoing review of clinical trial data focusing on data integrity,… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents ... The Associate Director, Clinical Sciences contributes to...through early and/or late phase development. Reports to the Sr Dir/Director, Clinical Science, Internal Medicine and… more
- Cardinal Health (Albany, NY)
- …Review agreements in support of various business transactions, including strategic sourcing, clinical trial services, confidentiality, Business Associate and ... other departments + Work under the general supervision of senior attorneys and exercise sound judgment as to matters...matters that require attention of Legal and Compliance Departments' senior leadership + Promote and ensure compliance with the… more
- Pfizer (New York, NY)
- …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... the reporting of clinical trial results to regulatory authorities and...* May independently present at department, project team, or Sr . Management meetings. * May lead inter-department projects involving… more
- Otsuka America Pharmaceutical Inc. (Albany, NY)
- …As core study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of... clinical , statistical, and regulatory literature for current clinical trial results, regulatory trends and new… more