in Williamsburg that focuses on Oncology patients. This role involves working with patients whose veins may not be as prominent... according to established procedures. Clearly and courteously explain the process of venipuncture and other specimen collections...
. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the... experience. 3+ years of data review experience in oncology and phase 1 clinical trials. Must have Phase I/Early Phase...
. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the... experience. 3+ years of data review experience in oncology and phase 1 clinical trials. Must have Phase I/Early Phase...
. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the... experience. 3+ years of data review experience in oncology and phase 1 clinical trials. Must have Phase I/Early Phase...
Lugar:
Cary, NC | 19/12/2024 21:12:51 PM | Salario: S/. No Especificado | Empresa:
Actalent to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe.... Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the...
Lugar:
New Jersey | 19/12/2024 19:12:19 PM | Salario: S/. No Especificado | Empresa:
Actalent. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the... experience. 3+ years of data review experience in oncology and phase 1 clinical trials. Must have Phase I/Early Phase...
. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the... experience. 3+ years of data review experience in oncology and phase 1 clinical trials. Must have Phase I/Early Phase...
Lugar:
New Jersey | 19/12/2024 18:12:38 PM | Salario: S/. No Especificado | Empresa:
Actalent. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves... to meet GCP, ICH, and regulatory requirements. Provide input into the drug development and evidence generation process...
Lugar:
New Jersey | 19/12/2024 03:12:31 AM | Salario: S/. No Especificado | Empresa:
Actalent. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves... to meet GCP, ICH, and regulatory requirements. Provide input into the drug development and evidence generation process...
. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves... to meet GCP, ICH, and regulatory requirements. Provide input into the drug development and evidence generation process...