Oncology CRA: Clinical Trials that Matter

GMP Technologies

Singapore

On-site

SGD 60,000 - 90,000

Full time

14 days+

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Job summary

GMP Technologies is seeking a Clinical Research Associate (CRA) specialized in oncology to join its clinical operations team. The role focuses on monitoring, data integrity, and regulatory compliance across sites, with an emphasis on patient safety and trial quality.

The ideal candidate holds a life sciences-related bachelor's degree (advanced degree preferred), at least 1 year of oncology clinical research experience, and solid knowledge of GCP, FDA/ICH guidelines, plus proficiency with MS

Qualifications

Bachelor's degree in life sciences, nursing, or related field; advanced degree preferred.
Minimum 1 year of oncology clinical research experience.
GCP, FDA regulations and ICH guidelines knowledge.
Excellent organizational and time-management skills.
Strong communication and teamwork abilities.

Responsibilities

Monitor clinical trials at investigative sites to ensure adherence to study protocols and regulatory requirements.
Conduct site initiation, routine monitoring, and close-out visits.
Review case report forms and source documents for accuracy and completeness.
Ensure timely data collection, entry and reporting.
Collaborate with investigators and site staff to address issues.
Assist in regulatory documents and ethics submissions.
Maintain study documentation and monitoring reports.