Clinical Monitoring

If you are a CRA working for a CRO or pharma and are looking to not travel as much... look no further this is your next career move.

We are a dedicated research facility with approximately 20 enrolling studies and 60 ongoing studies and need to expand our internal QA/QC department.  We are looking for both FT and PT QA/QC staff who have experience monitoring FDA regulated clinical research.  We take pride in the accuracy of our data and need someone who enjoys monitoring and wants to ensure our data is the best it can be.

Our ideal candidate would have 2+ years experience monitoring across multiple therapeutic areas as we conduct research in diabetes, cardiac disease, pain management and osteoporosis to name a few.  It would be beneficial if you have lead CRA and FDA audit experience as we are a top site that has had multiple FDA audits (none for cause).  The majority of our studies are Phase 2 and 3, however, we also have a Phase I unit with several ongoing studies.  Our studies are concentrated across multiple therapeutic areas: diabetes, hypertension, high cholesterol, obesity/weigh loss, fibromyalgia, arthritis, sexual dysfunction, osteoporosis and more.

Please only respond if you have experience reviewing subject charts in pharmaceutical research studies testing new medications and/or devices in human subjects.  We are not looking for candidates with bench research experience or lab research experience.  We are looking for candidates with GCP knowledge and experience (not GMP or GLP).  We are specifically seeking candidates who have monitored or audited clinical research studies at clinical research sites on behalf of a CRO, a sponsor or the FDA.  Our search is very narrow and specific.

We have an excellent PPO health care plan (100% paid by employer for the employee), 401 (K) with 4% company match, standard vacation and sick leave, and many employee appreciation programs.

Please provide your salary requirements with your response to this ad.