- Merck & Co. (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... internal policy, regulatory requirements, and health literacy principles.With minimal oversight, the Senior Informed Consent Medical Writer:Demonstrates… more
- Merck & Co. (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... policy, regulatory requirements, and health literacy principles.With oversight, the Informed Consent Medical Writer:Demonstrates growing independence… more
- Merck (Rahway, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
- Merck (Trenton, NJ)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
- J&J Family of Companies (Raritan, NJ)
- …required. Manages local study supply, as required. + Prepares country specific informed consent in accordance with procedural document/templates. Reviews and ... Learn more at https://www.jnj.com/innovative-medicine We are searching for a ** Senior , Local Trial Manager** **to be located remotely within...manages site specific informed consent forms in accordance with SOPs,… more
- Vitalief (New Brunswick, NJ)
- …CRC will perform protocol-specific tasks including: Surgical patient screening, obtaining informed consent , collection of protocol required imaging, IRB ... Operating Procedures (SOPs), and create SOPs as needed (ie, process for obtaining informed consent ; study subject data collection process, etc.). + Follow and… more
- Sanofi Group (Morristown, NJ)
- …Author medical related study documents (pre-defined deviation list, the Informed Consent Form, Written Subject Information, study specific committee charter, ... **Job title** : Senior Clinical Scientist **Location:** Cambridge, MA **About the...clinical development activities (eg pressure test and cluster feasibility, medical review and validation of clinical data, study risk… more
- Sumitomo Pharma (Trenton, NJ)
- … safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports ... signal evaluation reports according to established safety governance policies and keeping senior leadership informed of safety issues. **Job Duties and… more
- Taiho Oncology (Princeton, NJ)
- …documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study ... Executive Medical Director, Clinical Development Pleasanton, CA, USA *...study conduct and operational risks. Represent the molecule at senior management governance meetings. + Mentoring and training of… more
