Remote Senior Cardiovascular Clinical Research Associate

MSD; Florida; Remote; GBP 97,000 - 152,000; Full time

Job summary

Merck & Co., Inc. is seeking a Clinical Research Associate to drive site management and monitoring across multiple protocols, ensuring ICH-GCP compliance and high data integrity. The role involves coordinating with sponsors, investigators, and cross-functional teams to support site readiness and ongoing study conduct.

You will travel domestically and internationally up to 65–75% of time, mentor junior CRAs, and contribute to process improvements while maintaining rigorous regulatory standards.

Qualifications

• Experience in site management and monitoring activities.
• Knowledge of ICH-GCP and country regulations.
• Ability to mentor junior CRAs and work in cross-functional teams.

Responsibilities

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and related documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates & manages tasks with sponsor roles to achieve Site Ready.

Skills

Site management

Monitoring

Study coordination

Regulatory compliance

Mentoring

Education

Associate’s degree or equivalent

Bachelor’s degree in life sciences

Tools

CTMS

eTMF

SOPs

Job description

Merck & Co., Inc. is seeking a Clinical Research Associate to drive site management and monitoring across multiple protocols, ensuring ICH-GCP compliance and high data integrity. The role involves coordinating with sponsors, investigators, and cross-functional teams to support site readiness and ongoing study conduct.

You will travel domestically and internationally up to 65–75% of time, mentor junior CRAs, and contribute to process improvements while maintaining rigorous regulatory standards.