Senior Clinical Research Associate – Oncology

About the role

Syneos Health is seeking an experienced Senior Clinical Research Associate (CRA) to lead oncology studies for a single sponsor. The role involves both on‑site and remote monitoring to ensure compliance with GCP and regulatory standards.

Key responsibilities

• Conduct on‑site and remote monitoring of oncology clinical trials, reviewing protocols, informed consent forms, and case report forms.
• Develop monitoring plans, checklists, and templates to ensure high‑quality data collection.
• Prepare monitoring reports, follow‑up letters, and action plans documenting findings.
• Coordinate site visits, track study progress, and resolve operational issues.
• Collaborate with investigators, site staff, and cross‑functional teams to support smooth trial execution.

Required profile

• Bachelor’s degree in a related field or equivalent experience.
• 3‑4 years of clinical research monitoring experience, preferably in oncology.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and manage multiple priorities.

Required skills

• Proficiency with clinical trial management systems.
• Advanced use of Microsoft Office Suite.
• Certified Clinical Research Associate (CCRA) or equivalent certification preferred.