Phlebotomist

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...

Lugar: Williamsburg, VA | 24/12/2024 20:12:13 PM | Salario: S/. No Especificado | Empresa: Actalent

Clinical Research Scientist

. 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: Alameda, CA | 20/12/2024 02:12:39 AM | Salario: S/. No Especificado | Empresa: Actalent

Clinical Research Scientist

. 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: San Diego, CA | 20/12/2024 01:12:32 AM | Salario: S/. No Especificado | Empresa: Actalent

Clinical Research Scientist

. 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

Clinical Research Scientist

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

Clinical Research Scientist

. 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: Fort Lauderdale, FL | 19/12/2024 19:12:56 PM | Salario: S/. No Especificado | Empresa: Actalent

Clinical Research Scientist

. 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

Clinical Research Scientist

. 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

Clinical Research Scientist

. 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 York City, NY | 18/12/2024 23:12:39 PM | Salario: S/. No Especificado | Empresa: Actalent

Clinical Research Scientist

. 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: Philadelphia, PA | 18/12/2024 23:12:17 PM | Salario: S/. No Especificado | Empresa: Actalent