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Clinical Payments Associate Analyst

Type

Full time

Location
USA IRV-17211 Redhill/MLE
Job reference

Req-37104

Posted for

1 day ago

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.

Dedicated to innovation, our Surgical business unit is focused on identifying and solving critical, unmet needs in cardiac surgery. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patients’ quality of life and expand their potential treatment opportunities. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

As the Clinical Payments Associate Analyst, you will analyze, track and process payments associated with clinical trials, ensure alignment with contractual and trial requirements and manage the lifecycle of payments. Analyze patient data in clinical CRFs (Case Review Form) to determine alignment to protocol requirements, contracts and budget (i.e. SOW) to proceed with payment processing. Identify invoice and payment management tracking and process improvements via collaboration with cross-functional teams and cross BU teams. The position will be on-site at our Irvine headquarters.

How you’ll make an impact:

  • Lead and develop moderate to complex projects to drive clinical trial payment efficiencies which may include development of reports, dashboards, resource guides, and system evaluation (i.e. review of payment logic setup in CTMS, etc.)

  • Provide recommendations/awareness to management and/or key stakeholders proactively. Monitor and evaluate post process implementation performance and implement changes if necessary.

  • Interact proactively with clinical trial sites and vendors as well as internal functions and management to resolve payment inquiries, including reconciliations, analytics, and other ad hoc requests.

  • Perform routine analysis and contribute to activities and projects related to clinical trial payments, contract and budget development, and preparation of analytics and reports.

  • Analyze patient data in clinical CRFs (Case Review Form) to determine alignment to protocol requirements.

  • Collaborate with manager and/or team members to evaluate and carry out process design and improvements.

  • Interact with global HCPs, clinical trial sites, and vendors as well as internal functions and management to resolve inquiries, including reconciliations, analytics, and other ad hoc requests.

  • Monitor and evaluate post process implementation performance and implement changes if necessary. Provide awareness to team members/management.

What you’ll need (required):

  • Bachelors Degree or equivalent

  • 1 year of previous finance, analytics, clinical payments and/or budget related experience

What else we look for (preferred):

  • Previous clinical research/clinical trials experience

  • Complex payments experience (e.g, invoices, expenses) clinical and/or medical affairs contractual costs using current processing systems (e.g., COUPA, JDE).

  • Experience working medical device industry

Additional skills:

  • Understanding of quantitative methodologies, techniques and tools

  • Knowledge of local and global regulations (e.g., AdvaMed, Anti-Kickback, Antibribery, Sunshine Act

  • Understanding of Good Clinical Practices, ICH guidelines, AdvaMed code, clinical research ethics, and patient privacy laws (plus applicable local regulations, when country based)

  • Understanding of clinical study protocols, clinical trial materials, and clinical costs

  • Knowledge of concepts of clinical research and device development

  • Understanding of contracts and negotiations

  • Computer skills in Excel and PowerPoint and other MS Office Suite apps including Word and Access

  • Strong written and verbal communication skills and interpersonal relationship skills

  • Problem-solving, organizational, analytical and critical thinking skills

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.

For California, the base pay range for this position is $66,000 to $90,000 (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.   

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Job reference

Req-37104

Apply Now
Type

Full time

Location
USA IRV-17211 Redhill/MLE
Posted for

1 day ago


SHARE THIS JOB
Apply Now
About Edwards Lifesciences

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease and critical care monitoring


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COVID Vaccination Requirement Notice

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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