Director, Medical Safety Officer, Solid Tumor Oncology
J&J Family of Companies - Raritan, NJ
…+ Informed Consent Forms (ICF), including Risk Language + Safety Sections of Investigator 's Brochure (IB) and IB addenda + Safety sections of Clinical Study Reports
Created: 2024-06-23
Study Responsible Scientist
Kelly Services - Raritan, NJ
…research trial + Presents study status at internal/external meetings, including investigator meetings and governance committees + Trains and mentors local/central
Created: 2024-06-19
Medical Director/ Sr. Medical Director, Clinical Development
J&J Family of Companies - Raritan, NJ
…consultants in concert with senior clinical staff, in conducting IDMC and Investigator meetings as well as Advisory Boards. **Qualifications** An MD is required;
Created: 2024-05-28
Director, Safety Surveillance Physician (Oncology)
J&J Family of Companies - Raritan, NJ
…Events of Special Interest (RMPs identified risks) + PBRER activities + Investigator Brochure activities + Watchlist activities + Analysis of Designated Medical
Created: 2024-05-24
Principal Medical Writing Scientist, Oncology Late Development (1 of 2)
J&J Family of Companies - Raritan, NJ
…documents such as, but not limited to, clinical study reports, investigator 's brochures, study protocols, summary documents, risk management plans, regulatory
Created: 2024-05-24
Director, Medical Safety Officer, Neuroscience and Ophthalmology
J&J Family of Companies - Raritan, NJ
…+ Informed Consent Forms (ICF), including Risk Language + Safety Sections of Investigator 's Brochure (IB) and IB addenda + Safety sections of Clinical Study Reports
Created: 2024-05-04
Principal Medical Writing Scientist, Oncology
J&J Family of Companies - Raritan, NJ
…documents such as, but not limited to, clinical study reports, investigator 's brochures, study protocols, summary documents, risk management plans, regulatory
Created: 2024-04-04
Clinical Trials Manager, Clinical Operations- Oncology
Gilead Sciences, Inc. - Parsippany, NJ
…relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports + Must be able to
Created: 2024-06-26
Clinical Research Associate - Real World Evidence
IQVIA - Parsippany, NJ
…available for filing in the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP and local regulatory
Created: 2024-06-22
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Clinical Research Associate, Sponsor Dedicated
IQVIA - Parsippany, NJ
…documents are available for filing in the Trial Master File (TMF) verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP / ICH and local
Created: 2024-06-20
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