Management & Business Development Resume Samples
Director of Operations
Senior Vice President
Chief Financial Officer
Chief Operating Officer
Christie Gordon - Service Manager Resume Simple
A highly motivated, detail-oriented, and results-driven professional with over 15 years of experience in the healthcare industry. Strong background in customer service, sales, and management.
technical support, presentations, research, database, procurement
management, writing, organized, clinical
Developed and implemented a new process for the procurement of all data sources. Created and maintained a robust and effective system for the project.
Assisted in the development of database and presentations for research. Wrote manuscripts for publication. Conducted literature reviews. Prepared and presented posters.
Managed and maintained the budget and accounting of all laboratory supplies. Coordinated with the purchasing department to ensure that the purchase orders were in place.
Served as a technical resource for the project team. Performed data entry and statistical analyses. Analyzed and interpreted data.
Developed and implemented a new process for the product development and customer relations. The project was sold to customers and the client.
Contract Technical Writer
Organized and maintained project management system (e.g. Oracle, central and electronic). Managed the study team.
Assisted in writing and submitting regulatory documents for submission to the IRB. Maintained and updated the study files. Prepared and submitted regulatory documents.
Reviewed clinical data for completeness and accuracy, and to ensure that all study documents are accurate and complete. Identify potential adverse events and serious adverse events.
Worked in a team environment, developed and implemented a clinical trial for the study, writing and reviewing protocols, and creating and implementing the informed consent forms for the study.
As a clinical research Specialist, I was responsible for writing and submitting regulatory documents to the IRB. Also, reviewed and filed all study documents.
Assists in the development of study documents for the clinical trial. Ensures that all regulatory documents are submitted to the IRB.