Field Clinical Engineer Cover Letter

I am excited to be applying for the position of field clinical engineer. Please accept this letter and the attached resume as my interest in this position.

In the previous role, I was responsible for clinical recommendations and best practices based on AORN Guidelines and other governing bodies for clinical practice.

Please consider my qualifications and experience:

• Develop several key accounts where the FCE presence can produce maximum benefits, both to the company and to the FCE’s professional development - These key accounts should be resource centers to Abbott for IDE clinical trials, employee training and Advisory Boards
• Successful completion of the North American Society of Pacing and Electrophysiology (NASPE), Associated Professionals examinations in Electrophysiology and Pacing and Defibrillation
• Experience working in a broader enterprise/cross-division business unit model preferred - Applies an extensive technical expertise and/or a thorough specialized knowledge at the forefront of the clinical engineering profession
• Minimum of an A.S
• Requires Abbott-specific certification on percutaneous procedures and instrument usage and programming, immersion in clinical research and literature as needed
• Comfort level with clinical environment including potential exposure to infectious disease(s), radiation, blood borne pathogens
• English is mandatory (written & spoken), French is very appreciated
• Previous experience dealing with customers and representing the technical side of a company is desirable

In response to your job posting for field clinical engineer, I am including this letter and my resume for your review.

Previously, I was responsible for tactical and strategic oversight of clinical trials to ensure compliance across all Therapeutic Areas/ Clinical Operations.

My experience is an excellent fit for the list of requirements in this job:

• Operating procedures, processes, and task assignments
• Willing to work different shifts as business needs
• Assist in the site qualification, and initiation processes for TAVR trials in the US
• May assist in the development of the TAVR training plans/materials
• Assist in the clinical study procedure (sterile field), playing a key role in device preparation, providing technical support and device and system troubleshooting as needed
• Build credibility and trust with customers and team members by understanding, prioritizing and escalating needs, conducting pro-active regular customer/site visits and providing regular documented communications regarding status of assets and equipment
• Adopt, develop, educate, implement and socialize best practices with all levels of staff and management
• Independently resolve equipment and customer issues, completes PMs, FCOs, installations and diagnoses and resolves electronic, network, and mechanical problems

I submit this application to express my sincere interest in the field clinical engineer position.

In the previous role, I was responsible for guidance and direction to personnel engaged in research studies or clinical trials to ensure compliance with protocols and overall clinical objectives.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Previous medical device experience is desirable
• Proficient use of general MS Office software and operational software
• Experience in field service Engineering (IVD field would be advantage)
• Proficient in MS Office, MS Windows
• Possess driver's license and able to drive to meet business needs
• Able to communicate in both Thai and English
• Clinical Research experience in Medical Device
• Experience coordinating multi-center Cardiology trials

I would like to submit my application for the field clinical engineer opening. Please accept this letter and the attached resume.

In the previous role, I was responsible for day-to-day coordination of clinical research studies and conformance with all the requirements of the regulatory bodies.

Please consider my qualifications and experience:

• Prior experience with Robotics preferred
• Knowledgeable of the clinical trial process
• Working knowledge and interest in EP ablation procedures
• Knowledge of Microsoft Windows and Linux operating systems
• Direct technical experience and hands on healthcare experience with Connectivity, EMR, Data Integration and Monitoring Systems Solutions
• Project management/coordination skills and experience
• Related working experience in hospitals/cardiac technology, familiar with workflow and processes in the hospital preferred
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies

In response to your job posting for field clinical engineer, I am including this letter and my resume for your review.

In my previous role, I was responsible for compliance guidance on the conduct of clinical research division-wide,for developing and overseeing a quality training program and for compliance in all audits of the Clinical Research organization.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Perform quality assurance inspections and maintain service and calibration documentation in accordance with applicable codes, standards, and manufacturer recommendations
• Provide equipment planning and pre-purchase evaluations of new equipment to site and Clinical engineering management
• Activate, configure, test, install and educate staff on the RTLS/RFID Aeroscout Asset and Temperature Monitoring System
• Fresh graduates with sales/hospital/healthcare working experience preferred
• Experience in the management of clinical devices
• Cardiovascular/Cardiac rhythm management device training (e.g., pacemakers & defibrillators) strongly preferred
• Experience in a Cath lab, biomedical engineering, hospital/clinic or medical sales
• Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials