Associate Clinical Research Specialist Jobs in Michigan

Manages progress by tracking regulatory submissions, recruitment, case report forms (CRF) completion, and data query resolution

Assist sites with the IRB submission and renewal process and tracks continuing IRB renewals. Ensure site compliance with IRB requirements

3 – 5 years clinical research experience in medical device, pharmaceutical industry or CRO as a CRA

Strong working knowledge, understanding and ability to apply FDA regulations and ICH/GCP guidelines governing clinical trials

Excellent organizational skills along with strong attention to detail and the ability to keep detailed, accurate records

Strong verbal and written communication, superior organizational and interpersonal skills