Mid Level Monitoring and Evaluation Assistant Jobs

INTRODUCTION

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.

ROLE AND RESPONSIBILITIES

• Field monitoring of studies and data collection for clinical trials, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.
• Developing and delivering technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities. Acting as a mentor to new or junior level employees.
• Providing oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements.
• Validating investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.
• Verifying trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded.
• Editing/amending informed consent documents.

BASIC QUALIFICATIONS

• Bachelor's Degree or equivalent in related field with 5 years of field monitoring, quality assurance/control and regulatory compliance experience or equivalent work experience based on Edwards criteria.
• Ability to travel up to 75% domestically.

PREFERRED QUALIFICATIONS

• Clinical research certification (ACRP or SoCRA clinical coordinator / CRA certification).
• Experience in clinical trials of medical devices.
• Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills.
• Demonstrated problem-solving and critical thinking skills.
• Proven expertise in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery.
• Excellent understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise.
• Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting.
• Technical writing skills (protocols, CRF development, study tools).
• Ability to communicate and relate well with key opinion leaders and clinical personnel.
• Experience in training new hires.

COMPENSATION

• The base pay range for this position is $108,000 to $153,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.