Investigator Contracts Lead - Oncology
- United States
- ICON Strategic Solutions
- Contracts Administration
- Remote
About the role
Investigator Clinical Contracts Lead is responsible for direct site-facing contract and budget negotiations thought contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies.
What Do you Need to Have?
- Exercise good judgment in balancing the risks in making budget and contractual decisions against the impacts to clinical trial timelines.
- Follow GPD processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials.
- Work with partners to develop and oversee the global site budget process.
- Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters.
- Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface.
- Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space.
- Partner with Legal, Finance and other divisions to identify and implement areas of improvement in the site contracting space.
- Has knowledge of the principles, concepts and theories in applicable business discipline.
- Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements.
- Applies acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in applicable discipline.
- Draft, review, negotiate clinical trial contracts and associated clinical budgets.
- Must have Lead experience negotiating CTA's and budgets.
- Minimum 2 years of experience in clinical study contracts at pharma or CRO environment with a JD
- Minimum 5 years of experience in clinical study contracts at pharma or CRO environment without a JD
- Minimum 7 years clinical study contracts to be considered at the Senior level. With JD would need 2 years.
- Bachelor degree or graduation on law, finance, business administration, health science or related field - Required.
- Preferred soft skills: Negotiation capacity, proactivity, effective priorization & organization and problem solving mindset.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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