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Edwards Lifesciences Clinical Research Monitor (Midwest Region) – Transcatheter Mitral and Tricuspid Therapies (TMTT) in Des Moines, Iowa

The TMTT Clinical Affairs organization is a multi-functional team supporting the product development lifecycle through groundbreaking clinical trial design and execution.

The Clinical Research Monitor position is a field-based role located in the Midwest region of the United States. The primary responsibility will be to ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence.

Key Responsibilities

  • Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.

  • Provide 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 Committees, Clinical Operations (e.g. Contracts), and recommend and develop process improvements.

  • Verify 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.

  • Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.

  • Develop and deliver 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.

  • Contribute to the development of clinical protocols, informed consent forms, and case report forms.

  • Edit/amend informed consent documents.

Basic Qualifications

  • Bachelor’s degree in related field with 1-2 years of previous field monitoring experience

  • Associate’s degree in related field with 5 years of previous field monitoring experience

  • Experience working in a medical device or regulated industry

  • Experience with electronic data capture

Preferred Qualifications

  • Clinical research certification (ACRP or SoCRA clinical coordinator/ CRA certification)

Additional Expectations

  • Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills

  • Proven expertise in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery

  • Demonstrated problem-solving and critical thinking skills

  • Strong 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

  • Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

For Colorado Residents Only

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

The base pay range for this position is $91,000.00 to $107,000.00

Additional information can be found through the link below:

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

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.

For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.