MedTech Clinical Trial Specialist — Onsite Impact

Biopharma Careers; Cincinnati (OH); On-site; USD 92,000 - 148,000; Full time

Job summary

Johnson & Johnson MedTech is seeking a Clinical Trial Specialist to support trials at sites in Cincinnati, OH or Santa Clara, CA. The role requires full onsite work five days a week and a strong clinical research background.

The candidate will manage site initiation, monitoring, data accuracy, and regulatory compliance across trials, collaborating with the Clinical Trial Leader to ensure timely progress and high quality documentation.

Qualifications

• A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
• 3+ years of experience working in clinical trials is required; MS with at least 2 years, PhD with at least 1 year of related experience .
• Previous clinical research experience is required.

Responsibilities

• Act as primary local company contact for assigned sites for specific trials.
• Leads executional aspects of sponsored clinical trials with appropriate oversight.
• Participate in site feasibility and/or pre-trial site assessment visits.
• Attend/participate in investigator meetings as needed.
• Complete activities within site initiation and start-up, preparation and conduct of site monitoring and close-out according to SOPs, Work Instructions and policies.
• May develop clinical trial documents, such as monitoring plans, informed consent.
• Implement risk-based monitoring model at the site level and work with site to ensure timely resolution of issues found during monitoring visits.
• Work with Clinical Research Manager during site activation to speed up the process.

Skills

Clinical trials experience

Regulatory compliance

Microsoft Office

Presentation skills

Education

Bachelor's Degree in Life Science

Job description

Johnson & Johnson MedTech is seeking a Clinical Trial Specialist to support trials at sites in Cincinnati, OH or Santa Clara, CA. The role requires full onsite work five days a week and a strong clinical research background.

The candidate will manage site initiation, monitoring, data accuracy, and regulatory compliance across trials, collaborating with the Clinical Trial Leader to ensure timely progress and high quality documentation.