Edwards Lifesciences Veterans Jobs

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Edwards Lifesciences Senior Clinical Research Monitor - Transcatheter Mitral and Tricuspid Therapies - Texas - South West Region in Dallas, Texas

This is an exciting opportunity for you to join a team boldly designing transcatheter mitral and tricuspid therapies from the ground up. Edwards’ Transcatheter Mitral and Tricuspid Therapies team is deeply dedicated to solving the complex challenges of mitral and tricuspid disease in order to transform treatment and significantly improve patients’ lives around the world.

The Senior Clinical Research Monitor will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence.

This position will travel up to 75% south west Texas Region with nationwide flexiblity.

Responsibilities include, but not limited to:

  • 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.

  • Develop and deliver 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. Act as a mentor to new or junior level employees.

  • 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 Boards, Contract, and Training, developing process improvements.

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

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

  • 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.

  • Edit/amend informed consent documents.

Minimum Requirements:

  • Bachelor's Degree with 5 years of previous field monitoring experience

  • Associate's Degree with 7 years of previous field monitoring experience quality assurance/control and regulatory compliance experiencerequired

Preferred Qualifications: In addition to meeting minimum requirements, it would be nice to have the following:

  • Experience working in a medical device or regulated industry

  • Experience with electronic data capture

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

  • 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

  • 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

  • Experience in training new hires

  • 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

Additional Talents and General Expectations:

Clinical research certification (ACRP or SoCRA, Clinical Coordinator/CRA certification) Preferred

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.

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