Northern Texas Facial Oral Surgery invites you to become an integral part of our successful team...Job Description The Clinical Assistant helps the surgeon during consultations and surgeries...
Now hiring the following: Clinic Assistants This is an entry level billing position in a busy medical office. Prefer someone with medical billing experience and great customer service skills. High School diploma or GED required. Apply at 910-B S. Grant, Odessa, TX Closing date: Until filled EOE, M/F, D, V.
Capital Region Description Planned Parenthood of the Texas Capital Region PPTCR is Austin s leading...Employer Name PPTCR Planned Parenthood of the Texas Capital Region Description Planned Parenthood of the...
Employer Name PPTCR Planned Parenthood of the Texas Capital Region Description Summary Work as part...Clinic Assistant Austin Texas Job ID LL20091510 12720 Employer Name PPTCR...standing and walking Planned Parenthood in Austin Texas is an equal opportunity employer and celebrates...
Employer Name PPTCR Planned Parenthood of the Texas Capital Region Description Summary Work as part...Clinic Assistant Austin Texas Job ID LL20093108 12709 Employer Name PPTCR...Planned Parenthood in Austin Texas is an equal opportunity employer and celebrates...
***YOU MUST RESPOND WITH YOUR RESUME VIA THIS POSTING OR EMAIL TO CORI FRANKLIN TO BE CONSIDERED NO PHONE A global leader in the eye care industry in Fort Worth, TX is seeking an experienced Clinical Trials Assistant for a 6 month contract assignment. Contract could be extended based on performance and departmental workload. Initiating, preparing, and reviewing regulatory documents for clinical research study sites in order to ensure FDA and IRB compliance. Daily reports provided to study manager and lead
***YOU MUST RESPOND WITH YOUR RESUME VIA THIS POSTING OR EMAIL TO CORI FRANKLIN TO BE CONSIDERED NO PHONE CALLS-cori.franklin@na.manpower.com A global leader in the eye care industry in Fort Worth, TX is seeking an experienced Clinical Trials Assistant for a 6 month contract assignment. Contract could be extended based on performance and departmental workload. Initiating, preparing, and reviewing regulatory documents for clinical research study sites in order to ensure FDA and IRB compliance. Daily reports