Associate Clinical Research Monitor, Midwest

Edwards Lifesciences; Indiana (PA); Hybrid; USD 60,000 - 90,000; Full time

Job summary

Join a forward-thinking company dedicated to transforming patient care through innovative technologies. As an Associate Clinical Research Monitor, you will play a crucial role in ensuring the safety and compliance of clinical trials. You will work closely with medical professionals and regulatory authorities to monitor data, verify documentation, and provide insights into trial activities. This position offers the chance to make a significant impact on patient outcomes while working in a collaborative environment focused on excellence and innovation in healthcare. If you are passionate about clinical research and eager to contribute to groundbreaking advancements, this opportunity is for you.

Qualifications

• 1 year experience in field monitoring or clinical research.
• Understanding of cardiovascular anatomy and medical device regulations.

Responsibilities

• Monitor clinical trials for compliance with protocols and regulations.
• Validate data and maintain regulatory documents for trials.
• Provide training on GCPs and compliance requirements.

Skills

Field Monitoring

Regulatory Compliance

Data Analysis

Technical Writing

Communication Skills

Education

Bachelor's Degree in related field

Tools

MS Office (Word, Excel, Adobe)

Electronic Data Capture Systems

Job description

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

Patients with mitral and tricuspid heart valve disease often have complex conditions with limitedtreatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldlypursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s ourdriving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

We are searching for an Associate Clinical Research Monitor to join Edwards Tricuspid team based in the Midwest region. As the Associate Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence. The ideal candidate will reside in Midwest / Northeast region.

How you'll make an impact :

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.

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.

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 / Clinical Operations (e.g. Contracts), and recommend and develop process improvements.

Develop and deliver training on GCPs, protocols, and database, compliance, device accountability, and adverse event reporting.

Edit / amend informed consent documents.

Other incidental duties

What you'll need (Required) :

Bachelor's Degree or equivalent in related field

1 year experience field monitoring experience, quality assurance / control and regulatory compliance OR

1 year experience working in an environment with hands-on clinical research experience encompassing all aspects of the clinical process, including 1) Cardiovascular device trials; and 2) Cath lab, operating room and / or intensive care unit familiarity, preferred

Ability to travel up to 75% for clinical site visits

What else we look for (Preferred) :

Substantial computer literacy in MS Office, to include Word, Excel, Adobe and ability to operate general computer software and office machinery

Understanding of cardiovascular anatomy, pathology and physiology

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 with electronic data capture

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

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

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Clinical Research Associate • USA, Indiana, Remote