Clinical Trial Liaison - Heart Failure Device Studies

Impulse Dynamics; New Jersey; On-site; USD 115,000 - 125,000; Full time

Benefits offered by this job

Full coverage medical benefits

Paid vacation and holidays

401k match

Job summary

Impulse Dynamics is seeking a Clinical Trial Liaison for the Northeast USA to manage clinical sites through start-up, recruitment, device implantation, and follow-up phases. You will coordinate with regulatory, clinical, and vendor teams to ensure compliant study execution.

The ideal candidate has 5+ years in life sciences or biomedical engineering, strong clinical research experience, and familiarity with GCP, ISO, and 21 CFR guidelines. Competitive salary and benefits listed.

Qualifications

• 5+ years experience in Life, Health Sciences, Nursing or Biomedical Engineering field
• 5+ years experience in Clinical research
• Familiarity with Good Clinical Practice, ISO and 21 CFR regulations pertaining to clinical research

Responsibilities

• Manage assigned clinical sites during the lifecycle of clinical research, including start-up, recruitment, device implantation, and follow-up
• Support site initiation visits, clinical education, data collection oversight, and subject recruitment strategies
• Communicate with site staff and investigators to ensure successful completion of studies
• Attend clinical cases and study follow-up visits to ensure proper data collection and adherence to protocol
• Ensure regulatory requirements of clinical trial reporting are met accurately and expeditiously
• Capture clinical experiences at sites to improve product understanding and acceptance

Skills

Clinical research

Medical device industry

Relationship development

Communication

Regulatory knowledge

Education

Bachelor's degree in Life Sciences/Nursing/Biomedical Engineering

Job description

Impulse Dynamics is seeking a Clinical Trial Liaison for the Northeast USA to manage clinical sites through start-up, recruitment, device implantation, and follow-up phases. You will coordinate with regulatory, clinical, and vendor teams to ensure compliant study execution.

The ideal candidate has 5+ years in life sciences or biomedical engineering, strong clinical research experience, and familiarity with GCP, ISO, and 21 CFR guidelines. Competitive salary and benefits listed.