Senior Clinical Trial Coordinator – Remote & SME Leader

Regulatory Jobs; Rahway (NJ); Remote; USD 74,000 - 118,000; Full time

Benefits offered by this job

Remote work

Flexible work arrangements

Comprehensive benefits package

Job summary

Merck & Co., Inc., Rahway, NJ, USA is seeking a Clinical Trial Coordinator with a strong focus on regulatory submissions and governance. You will support trial start-up, maintain trial documents, and collaborate with cross-functional teams to ensure timely, compliant study execution.

The role involves coordinating with investigators, preparing IRB/ERC submissions, and maintaining CTMS records while mentoring junior team members. A flexible work arrangement and comprehensive benefits are offered.

Qualifications

• Minimum 3 years in Clinical Research or healthcare.
• Completed job training (office management, administration, finance, health care) or Bachelor's Degree.
• Fluent in local languages and business proficient in English.

Responsibilities

• Track essential documents and report safety events.
• Collaborate with local teams on budgets and CTRAs.
• Prepare submission packages for IRB/ERC and health authorities.
• Update CTMS and study tools.
• Mentor junior CTCs and drive process improvements.

Skills

Clinical Research

Clinical Trial Agreements (CTA)

GCDMP

Time Management

Microsoft Excel

CTMS

Regulatory Knowledge

Education

Bachelor's Degree

Job description

Merck & Co., Inc., Rahway, NJ, USA is seeking a Clinical Trial Coordinator with a strong focus on regulatory submissions and governance. You will support trial start-up, maintain trial documents, and collaborate with cross-functional teams to ensure timely, compliant study execution.

The role involves coordinating with investigators, preparing IRB/ERC submissions, and maintaining CTMS records while mentoring junior team members. A flexible work arrangement and comprehensive benefits are offered.