Senior Clinical Research Associate I — Global Monitoring & Site Lead

Novotech Health Holdings; Philippines; On-site; PHP 600,000 - 1,000,000; Full time

Job summary

Novotech Health Holdings is seeking a Clinical Research Associate (CRA) to manage and monitor clinical projects in line with ICH-GCP, SOPs, and PMP. You will contribute to protocol development, perform site qualification/monitoring visits (onsite or remote), and ensure regulatory compliance across study sites.

The role requires a BS in a science field, 3+ years in clinical research, strong English communication, and meticulous attention to detail.

Qualifications

• 4-year BS degree or equivalent.
• Advanced degree is a plus.
• At least 3 years of experience in clinical research.
• Good command of written and spoken English.
• Good organization and communication skills.
• High attention to detail and accuracy.

Responsibilities

• Contribute to protocol and ICF development and other documents.
• Perform site qualification, initiation, monitoring and close-out visits (on-site or remote).
• Ensure regulatory, ICH-GCP and project requirements are met.
• Escalate serious issues and support action plans with the team.
• Provide training or mentorship to junior CRA staff as needed.

Skills

English proficiency

Communication skills

Organization skills

Detail-oriented

Education

Bachelor of Science in related field

Advanced degree preferred

Job description

Novotech Health Holdings is seeking a Clinical Research Associate (CRA) to manage and monitor clinical projects in line with ICH-GCP, SOPs, and PMP. You will contribute to protocol development, perform site qualification/monitoring visits (onsite or remote), and ensure regulatory compliance across study sites.

The role requires a BS in a science field, 3+ years in clinical research, strong English communication, and meticulous attention to detail.