Senior Clinical Trial Coordinator - Remote Process SME

MSD; Oregon; Hybrid; USD 74,000 - 118,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k)

Job summary

Merck & Co., Inc. seeks a Clinical Trial Coordinator to handle trial and site administration, document control, regulatory submissions, and budgeting tasks. You will work with COM, CRM and CRA, maintain CTMS/databases, manage labeling and translations, and support CTRAs and payments while ensuring GCP compliance.

The role emphasizes SME-level process improvements, mentoring junior staff, and contributing to on-site readiness and study deliverables.

Qualifications

• Fluent in English (verbal and written) and strong communication skills.
• Knowledge of Global/Regional Clinical Research guidelines.

Responsibilities

• Manage trial and site administration including essential documents and safety reports.
• Maintain CTMS and study trackers, and coordinate clinical and non-clinical supply management.
• Assist with IRB/ERC submissions and regulatory agency processes.
• Support budgeting, contracts (CTRAs) and payments, ensuring compliance.

Skills

Fluent English

Good communication

MS Excel

Time management

CTMS knowledge

GCP knowledge

Education

Bachelor's Degree

Tools

CTMS

Job description

Merck & Co., Inc. seeks a Clinical Trial Coordinator to handle trial and site administration, document control, regulatory submissions, and budgeting tasks. You will work with COM, CRM and CRA, maintain CTMS/databases, manage labeling and translations, and support CTRAs and payments while ensuring GCP compliance.

The role emphasizes SME-level process improvements, mentoring junior staff, and contributing to on-site readiness and study deliverables.