Remote Clinical Trial Coordinator Site & Docs Lead

Merck; Juneau (AK); Remote; USD 68,000 - 107,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

401(k) retirement plan

Medical, dental, vision insurance

Job summary

Merck is seeking a Clinical Trial Coordinator to support trial and site administration, ensure proper documentation, and collaborate with COM/CRM/CRA teams. You will assist with regulatory submissions, CTRAs, and payments while maintaining CTMS and study tools, aiming to meet Site Ready dates and budget targets.

Responsibilities include coordinating labeling, translations, and eTMF activities, organizing meetings, and ensuring quality control and compliance across the study lifecycle.

Qualifications

• Bachelor's degree or higher in a related field.
• Experience with clinical documentation management and GCP guidelines.
• Strong IT skills and proficiency in MS Office; CTMS familiarity preferred.

Responsibilities

• Oversee trial and site administration and manage essential documents.
• Update CTMS and tracking tools; coordinate labelling and translations.
• Support site start-up, regulatory submissions and insurance certificates.
• Develop and monitor country/site budgets; manage CTRAs and payments.
• Plan meetings and prepare study memos; ensure timely project reporting.

Skills

ClinicalDocumentManagement

ClinicalResearch

ClinicalTrialDocumentation

ClinicalTrialManagement

ClinicalTrialsMonitoring

ClinicalTrialsOperations

ClinicalTrialSupport

CustomerFocused

MicrosoftExcel

MicrosoftOffice

Education

Bachelor’s Degree or higher

Tools

CTMS

Job description

Merck is seeking a Clinical Trial Coordinator to support trial and site administration, ensure proper documentation, and collaborate with COM/CRM/CRA teams. You will assist with regulatory submissions, CTRAs, and payments while maintaining CTMS and study tools, aiming to meet Site Ready dates and budget targets.

Responsibilities include coordinating labeling, translations, and eTMF activities, organizing meetings, and ensuring quality control and compliance across the study lifecycle.