Senior Clinical Research Associate – Oncology Experience

This is a fully remote position, open to applicants in Belgium.

📋 Description

• Supervision of Monitoring Duties and Study Implementation.

• Guaranteeing adherence to regulatory standards, ICH-GCP, and protocol requirements.

• Utilizes judgment to assess the overall effectiveness of the site and its personnel.

• Keeps up-to-date with ICH/GCP Guidelines and relevant regulations.

• Confirms that informed consent has been executed correctly.

• Performs reviews and validations of source documents and site records.

• Oversees the reporting of protocol deviations and subsequent follow-ups.

• Records activities through follow-up correspondence and monitoring reports.

• Works in partnership with the primary Site Manager and site staff.

⛳️ Requirements

• Experience in oncology trials and familiarity with RECIST criteria is crucial.

• Skills in networking and relationship development.

• Effective and appropriate communication skills with both internal and external stakeholders.

• Capacity to adjust to evolving technologies and procedures.

• Proficient in the local language.

• Advanced proficiency or fluency in English is necessary.

• Bachelor’s degree or Registered Nurse (RN) in a relevant field or an equivalent mix of education, training, and experience.

🏝️ Benefits

• N/A