Analyst, Clinical Contracts and Budgets

Edwards; Irvine, Northern (CA, KY); Hybrid; USD 68,000 - 96,000; Full time

Benefits offered by this job

Competitive salary

Performance-based incentives

Benefits programs

Job summary

Edwards Lifesciences, a leader in transcatheter heart valve solutions, is seeking a Clinical Contracts and Budgets Analyst for a hybrid role near Irvine, CA. You will draft and negotiate NDAs, Master Clinical Trial Agreements, Scopes of Work, Trial Budgets, and Trial Purchase Agreements, ensuring compliance with regulations and Edwards policies.

You will collaborate with study teams and legal to mitigate risks, monitor timelines, and support site activations while maintaining high attention to

Qualifications

• Bachelor’s degree with 3 years of contract negotiation/administration and financial tracking/analysis against contracts or equivalent experience.
• Healthcare‑related contracts experience preferred as Edwards criteria.

Responsibilities

• Draft, redline, and negotiate moderately complex clinical contracts (NDA, Master CTA, SOW, Budget, TPA).
• Identify risks and advise management on mitigation.
• Analyze need for amendments or renewals and negotiate terms.
• Track timelines and impact on deliverables with stakeholders.
• Submit drafts for CLM approvals and signatures within authority.
• Partner with cross‑functional teams to implement process improvements.

Skills

Contract negotiation

Financial analysis

Cross-functional collaboration

Communication skills

Attention to detail

Education

Bachelor’s degree in related field

Contract or paralegal certification

Tools

CLM

MS Office

Job description

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.

Aortic stenosis impacts millions of people globally, yet it often remains under‑diagnosed and under‑treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life‑changing solution for patients by offering heart valve replacement without the need for open‑heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. 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 Contracts and Budgets Analyst, you will draft and negotiate Non‑Disclosure Agreements, Master Clinical Trial Agreements, Scopes of Work, Trial Budgets, and Trial Purchase Agreements for clinical trials, ensuring all terms and conditions comply with applicable regulations and guidelines.

This is a hybrid role (office and remote blend). Selected candidate must reside within a reasonable distance from the Irvine corporate location and have the ability to commute on required onsite days.

How you'll make an impact:

• Initiating, drafting, redlining, and negotiating moderately complex clinical related contracts (Non-Disclosure Agreements, Master Clinical Trial Agreements, Scope of Work, Trial Budgets, Trial Purchase Agreements) based on substantial knowledge policy and regulations governing Clinical Trials and Edwards Policy.
• Identifying risks (e.g. site incentives, legal issues, conflict of interest) and actively engaging with management to provide recommendations for mitigation. Providing clinical input on functional contract terms.
• Analyzing need for contract and budget amendments or renewals and making recommendations, and/or negotiating changes to terms and conditions.
• Identifying risk associated with project timelines set by project teams, impacting team’s deliverables and timelines, and key stakeholders’ workload (e.g., Legal Compliance, legal contracts, legal privacy, and risk management) based on revised timelines.
• Submitting proposed final draft and supporting documentation through ECLM or CLM system for contract approval and securing appropriate signatures within specified signing authority.
• Identify opportunities for process improvement in collaboration with cross-functional teams; present and implement process improvement plans to management and/or key stakeholders.

What you'll need (Required):

• Bachelor’s degree in related field with 3 years of previous related work experience in contract negotiation/administration and financial tracking/analysis against contracts, or equivalent work experience based on Edward's criteria.
• Experience in healthcare‑related contracts or equivalent work experience based on Edward's criteria.

What else we look for (Preferred):

• Contract or paralegal certification or equivalent work experience based on Edward's criteria.
• Strong experience with drafting and routing contracts in a Contract Life Cycle Management System (CLM).
• Proven expertise in Microsoft Office Suite including Word, PowerPoint, Access, Excel, and SharePoint.
• Extensive knowledge and understanding of Edwards policies, procedures, and guidelines relevant to contract negotiation and administration.
• Extensive understanding of the NDA, MCTA, SOW, and TPA templates and drafting to negotiate and redline contractual language.
• Understanding of medical device trials, GCP, and compliance requirements.
• Ability to collaborate with the Study Team and Clinical Project Manager to strategize on site prioritization and enable fast site activation.
• Advanced written and verbal communication skills and interpersonal relationship skills.
• Proven problem‑solving, organizational, analytical, and critical‑thinking skills.
• Ability to work in a team environment, including inter‑departmental teams and representing the organization on specific projects.
• Ability to build internal/external working relationships.
• Strict attention to detail.
• Ability to manage competing priorities in a fast‑paced environment.
• Ability to interact professionally with all organizational levels.

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 (CA), the base pay range for this position is $68,000 to $96,000 (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 Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world‑class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient‑focused culture to deliver life‑changing innovations to those who need them most.

Edwards Lifesciences is an equal opportunity employer. We believe that diversity and inclusion are essential to creating an environment where all our employees can grow and thrive. Guided by our values of integrity and service, we are committed to maintaining a culture of inclusivity and belonging by creating a welcoming workplace for people of all backgrounds.

Edwards Lifesciences is committed to providing reasonable accommodations and adjustments to individuals with a disability or neurodivergence. If you need an accommodation or adjustment during the application, interview, or hiring process, please see the disability accommodation section below.