Sandra

Medical Assistant/Research Patient Navigator

Organize townhall meetings throughout rural areas to discuss oncology clinical trials.. Obtain patient medical history, vital signs, administer injections, laboratory specimen collection, data entry.

Lab Assistant/Phlebotomist

Obtain laboratory specimens. Process laboratory specimens

Clinical Research Coordinator

Conduct phase I-IV Oncology clinical research studies.. Maintain regulatory binders, subject enrollment, screening procedures, adherence to protocol schedule.

Clinical Research Coordinator

Certified Clinical Research Coordinator

Clinical Research Coordinator

Budget & Contract negotiations, IRB submission, source document design, subject enrollment, scheduling study visits, obtain vital signs, ECG, laboratory specimen collection and processing, EDC entry.

Clinical Research Coordinator

Site Director/Clinical Research Coordinator

Negotiate budgets and contracts.. IRB document submission.. Screen & enroll subjects.. Design source documents specific to each protocol.. Train research coordinator's.

Certified Clinical Research Coordinator

Source document design, subject enrollment, obtain vital signs, ECG, collect laboratory specimens, process laboratory specimens, maintain all study specific logs, maintain regulatory binders.

Certified Clinical Research Coordinator

Screening and enrollment, Central and Local IRB submission, source document design, EDC entry, Phlebotomy, processing and shipment of all biological samples, schedule study visits.

Certified Clinical Research Coordinator

Perform skin testing, spirometry, design source documents, informed consent, budget and contract negotiations, maintain all study related documents, IRB document completion and submission.

Phlebotomist/Lab Assistant