Clinical Research Associate - Oncology (Remote)

Merck · Rahway, NJ

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Clinical OperationsFull-time$96k–$151kCompany career page

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Role summary

Clinical Research Associate supporting oncology studies at Merck, responsible for site management, regulatory compliance, and monitoring across assigned protocols. Role involves ensuring adherence to ICH-GCP standards, conducting site visits, and managing relationships with investigators and study sites throughout all trial phases.

What they're looking for

Fluent in local languages and English with excellent verbal and written communication skills
Strong understanding of clinical trial phases, GCP/ICH guidelines, and country-specific clinical research regulations
Proficiency with Microsoft Office, clinical IT applications, and ability to adapt to new software on multiple devices
Demonstrated site management and patient recruitment skills with independent professional judgment
Good Documentation Practices knowledge and data analysis capabilities
Valid driver's license preferred

What you'll be doing

Develop and maintain relationships with assigned study sites throughout all trial phases and ensure regulatory compliance
Conduct site monitoring activities including validation, initiation, monitoring, and closeout visits using remote and on-site methods
Identify, assess, and resolve site performance and compliance issues in collaboration with management and cross-functional teams
Collect, review, and manage regulatory documentation for study startup, maintenance, and closeout activities
Identify and develop new potential clinical research sites according to country strategy and contribute site selection insights

Key requirements

Therapeutic area: Oncology

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