MedTech Clinical Trials Lead – Onsite & Site Management

Johnson & Johnson MedTech; Cincinnati (OH); On-site; USD 92,000 - 148,000; Full time

Benefits offered by this job

Vacation

Sick time

Holiday pay

Parental Leave

Volunteer Leave

Job summary

Johnson & Johnson MedTech is recruiting a Clinical Trial Specialist to manage trial sites, ensure protocol compliance, and support study execution. The role is based in Cincinnati, OH or Santa Clara, CA and requires full onsite work five days a week.

You will lead monitoring, data validation, CAPA coordination, and collaboration with CTLs, CROs, and site staff; travel up to 40% domestically is possible. Requires life sciences background and clinical trials experience.

Qualifications

• Bachelor degree required, life sciences preferred.
• 3+ years in clinical trials; MS with 2+ years or PhD with 1+ year acceptable.
• Experience with medical device trials and regulatory environments preferred.

Responsibilities

• Act as primary local contact for assigned trial sites.
• Lead executional aspects of sponsored trials with oversight.
• Participate in site feasibility and pre-trial visits.

Skills

Clinical trials

Documentation

Presentations

CAPA

Education

Bachelor's degree in Life Science/Related

Tools

Microsoft Office

Clinical systems

Job description

Johnson & Johnson MedTech is recruiting a Clinical Trial Specialist to manage trial sites, ensure protocol compliance, and support study execution. The role is based in Cincinnati, OH or Santa Clara, CA and requires full onsite work five days a week.

You will lead monitoring, data validation, CAPA coordination, and collaboration with CTLs, CROs, and site staff; travel up to 40% domestically is possible. Requires life sciences background and clinical trials experience.