Senior Clinical Research Associate - Remote South Florida

MSD; New Jersey; Teletrabalho; USD 129 000 - 203 000; Tempo integral

Resumo da oferta

Merck & Co., Rahway, NJ, USA is seeking an experienced Clinical Research Associate to manage site performance and monitoring across protocols, ensuring ICH/GCP compliance. The role includes developing site relationships, coordinating visits, documenting findings, and mentoring junior CRAs.

The primary location is USA - New Jersey (Rahway). Travel up to 75% domestically and internationally, with some remote work options.

Qualificações

• Fluent Spanish speaking skills required.
• Associate’s degree, certificate or equivalent in a scientific / healthcare discipline together with at least 7 years of relevant experience in the healthcare field, including at least 4 years of direct site management (monitoring) experience in bio / pharma / CRO.
• Bachelor’s degree (or above) with at least 4 years of direct site management (monitoring) experience in a bio / pharma / CRO.

Responsabilidades

• 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 associated documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Participates & provides inputs on site selection and validation activities.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure data quality and patient safety.

Formação académica

Associate degree / certificate or equivalent

Bachelor’s degree or above

Ferramentas

CTMS

eTMF

MS Office

Descrição da oferta de emprego

Merck & Co., Rahway, NJ, USA is seeking an experienced Clinical Research Associate to manage site performance and monitoring across protocols, ensuring ICH/GCP compliance. The role includes developing site relationships, coordinating visits, documenting findings, and mentoring junior CRAs.

The primary location is USA - New Jersey (Rahway). Travel up to 75% domestically and internationally, with some remote work options.