Barbara Rosales - Clinical Research Coordinator Resume Simple
A clinical research coordinator with a strong background in the pharmaceutical industry. I have extensive experience in the medical field. I have worked in the areas of study and research as a clinical research coordinator.
Provided data management for the design, collection, and interpretation of medical research studies. Trained in the use of the following: oncology, Neurology, cardiac, pulmonary, and metabolic.
Managed the day-to-day activities of the study team including assisting with the preparation of protocols, amendments, continuing reviews, and annual reports.
Prepared and submitted regulatory documents for submission to IRB. Managed and maintained study files. Monitored and documented all study related documents.
Maintained accurate records of study activity, including adverse events, serious adverse events, and drug reactions. Ensures that all pertinent information is documented and reported in a timely manner.
Conducted subject visits and performed vital signs, ECGs, and blood draws. Prepared and shipped specimens for shipment.
Ensured that all study related documents were completed and filed in a timely manner. Ensured that all serious adverse events (SAEs) are reported.
Process Engineering Technician
As a quality control Technician, I was responsible for the production and workflow of the lab. I was also responsible for the training of new employees.
Conducted audits of all employees and provided feedback to the team. Assisted in the development of new policies and procedures.
Managed and maintained the daily operations of the department, including communication with all departments. Assisted in the development of new and existing policies and procedures.
Assist in the development of the quality assurance program. Perform all aspects of the construction and maintenance of the equipment.
Provided technical support to the customer and client. Assisted in the development of new products. Implemented and maintained quality control systems.