Senior Clinical Research Associate – Oncology Experience

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

📋 Description

• Oversight of monitoring duties and study execution.

• Ensuring compliance with regulations, ICH-GCP, and study protocols.

• Verifying that the informed consent process is properly conducted and documented for each participant as required.

• Conducting reviews of source documents and verifying the accuracy of relevant site source documents.

• Managing the reporting of protocol deviations and ensuring appropriate follow-up actions are taken.

• Documenting activities through follow-up letters, monitoring reports, communication logs, and other necessary project documents in accordance with SOPs, CMP, and SMP.

• Overseeing site-level activities and communications to guarantee that project goals, deliverables, and timelines are achieved.

⛳️ Requirements

• Experience in oncology trials and knowledge of RECIST criteria.

• Strong networking and relationship-building abilities.

• Capable of effective and appropriate communication with both internal and external stakeholders.

• Adaptability to evolving technologies and processes.

• Exceptional communication (both verbal and written), presentation, and interpersonal skills.

• Ability to identify and cultivate effective relationships with investigator site personnel and other stakeholders.

• Proficiency in the local language is mandatory.

• Advanced level or fluency in English is essential.

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

🏝️ Benefits

• Flexible work arrangements.