Employment

Field Clinical Engineer

The primary responsibilities of our Field Clinical Engineer (FCE) include but are not limited to identifying and managing clinical investigational sites; working with hospital IRBs for approval of the Impulse Dynamics investigational units for clinical studies; participating in implants and follow ups, developing rapport with key cardiologists; serving as a technical resource between engineering, clinical research, and the medical community; and training investigational physicians and their respective staffs.

Bachelor's Degree in Engineering, Biological Sciences, a related field, or equivalent. A minimum of five plus years of progressively more responsible relevant clinical work experience in cardiology, electro-physiology, or working with ICD's, pacemakers, cardiac electro-physiology procedures or other electro implantable devices. Broad cross-disciplinary and in-depth knowledge of the clinical engineering profession. Comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, follow-up skills, and the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees, management, and customers.

Qualified candidates should submit a WORD version resume to resume@almyrainc.com

Field Clinical Specialist (Monitor)
The responsibilities of our Field Clinical Specialists include timely reporting and day to day management of the clinical data recorded during the course of the sponsored trials.

Essential Functions:
 

• Orient site personnel to study protocol/procedures
• Monitor compliance to FDA Regulations
• Monitor and promote compliance to local IRB reporting regulations
• Manage study site activities through frequent on-site visits
• Perform initial, interim and closeout study visits  
• Communicate findings to investigators and study staff at the site
• Prompt reporting of compliance issues to in-house staff

Position Specifications:

• Requires a RN, BS or similar degree (CRCC) with at least 2 years experience in monitoring clinical studies.
  
• The candidate must be very familiar with all FDA regulations governing IDE clinical trials.
  
• Excellent organizational skills and analytical and problem solving abilities
  
• Strong verbal and writing skills and interpersonal skills
  
• Strong PC skills include Windows environment, Excel and internet