Translational Research in Oncology is hiring for work from home roles

Translational Research in Oncology

8 Remote Job Openings at Translational Research in Oncology

Translational Research in Oncology is hiring for remote Clinical Research Associate

Clinical Research Associate

Translational Research in Oncology · Full Time · a month ago
Translational Research in Oncology
🌎 France 💵 €52500 - €61250 per year ⭐ 2-5 yrs exp 💼 Healthcare
The CRA is responsible for conducting site visits, ensuring adherence to FDA and ICH-GCP regulations, and performing data verification. Additional duties include managing regulatory documents, assisting with budget negotiations, and mentoring junior team members.
Translational Research in Oncology is hiring for remote Clinical Research Associate-Freelance

Clinical Research Associate-Freelance

Translational Research in Oncology · Full Time · 2 months ago
Translational Research in Oncology
🌎 Ireland ⭐ 2-5 yrs exp 💼 Healthcare
The CRA is responsible for conducting site visits and performing data verification to ensure compliance with FDA and ICH-GCP guidelines. Additional duties include managing regulatory documents, resolving data queries, and mentoring junior team members.
Translational Research in Oncology is hiring for remote Senior Clinical Research Associate

Senior Clinical Research Associate

Translational Research in Oncology · Full Time · 2 months ago
Translational Research in Oncology
🌎 Italy 💵 €55000 - €65000 per year ⭐ 5-10 yrs exp 💼 Healthcare
The role involves conducting various site visits and ensuring strict adherence to FDA, ICH-GCP, and local regulations. Responsibilities also include data verification, regulatory document collection, and mentoring junior team members.
Translational Research in Oncology is hiring for remote Clinical Research Associate-Freelance

Clinical Research Associate-Freelance

Translational Research in Oncology · Full Time · 2 months ago
Translational Research in Oncology
🌎 Ireland ⭐ 2-5 yrs exp 💼 Healthcare
The CRA is responsible for performing data verification, conducting site visits, and ensuring compliance with FDA and ICH-GCP guidelines. They will also assist with budget negotiations, data validation, and the collection of regulatory documents.
Translational Research in Oncology is hiring for remote Clinical Research Associate

Clinical Research Associate

Translational Research in Oncology · Full Time · 2 months ago
Translational Research in Oncology
🌎 Italy ⭐ 2-5 yrs exp 💼 Healthcare
The role involves conducting various site visits and ensuring strict adherence to FDA, ICH-GCP, and local regulations. Responsibilities also include performing data verification, managing regulatory documents, and mentoring junior team members.
Translational Research in Oncology is hiring for remote Clinical Research Associate

Clinical Research Associate

Translational Research in Oncology · Full Time · 3 months ago
Translational Research in Oncology
🌎 Italy ⭐ 2-5 yrs exp 💼 Healthcare
The Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and performing data verification. Additionally, the role involves mentoring junior team members and assisting with budget negotiations and query resolution.
Translational Research in Oncology is hiring for remote Senior Clinical Research Associate

Senior Clinical Research Associate

Translational Research in Oncology · Full Time · 4 months ago
Translational Research in Oncology
🌎 Italy 💵 €55000 - €65000 per year ⭐ 5-10 yrs exp 💼 Healthcare
The Senior Clinical Research Associate is responsible for conducting site visits, including pre-study, initiation, monitoring, and termination. They also ensure compliance with FDA and ICH-GCP regulations while mentoring junior team members.
Translational Research in Oncology is hiring for remote Senior Clinical Research Associate

Senior Clinical Research Associate

Translational Research in Oncology · Full Time · 6 months ago
Translational Research in Oncology
🌎 Italy 💵 €55000 - €65000 per year ⭐ 2-5 yrs exp 💼 Healthcare
Responsibilities include conducting various site visits such as pre-study, initiation, monitoring, and termination, while confirming adherence to all FDA, ICH-GCP, and local regulations. The role also involves ensuring the completion and collection of regulatory documents and performing data verification of source documents.