Clinical Trial Manager (Contracts & Payments)

ICON

  • Brasil
  • Permanente
  • Período integral
  • Há 9 horas
We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation.By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON's success as an industry leader.Full ServiceFull-service roles offer the opportunity to work on projects and programmes on behalf of the world's most innovative pharma, biotech and medical device companies.ICON Strategic SolutionsOur Strategic Solutions team is embedded in our clients' businesses, helping to deliver cutting edge research.Government and public health servicesWith our Government and Public Sector Solutions (GPHS) team you could be on the ground helping to resolve a crisis or having an impact on global health issues.Global Business ServicesGlobal Business Services functions are the backbone of the organisation, providing support services in areas including Finance, IT, HR, Sales, QA, Facilities & Administration, Legal & Procurement.Commercial roles offer opportunities to be involved in the exciting world of proposals, sales and marketing.Overview of Service LinesICON offers a broad range of specialised services to assist pharmaceutical, biotechnology and medical device companies to bring new drugs and devices to market faster. Our services span the entire lifecycle of product development and can be adapted to suit small local trials or large global programs.
  • Our Locations
Our LocationsWith headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries.
  • Why ICON?
Why ICON?No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples' lives, right across the world.Why icon? full service mean for you?Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula.Events? full service mean for you?Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. * Early TalentEarly TalentEarly talent programs are designed to provide participants with opportunities to gain valuable experience, develop their skills, and build relationships with experienced leaders within the organization. Early talent programs can take many forms, including internships, academy programs, and leadership development programs. ICON is committed to recruiting top talent while also fostering a culture of learning and development within the organization.graduate What does full service mean for you?Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula.Clinical Trial Manager (Contracts & Payments)
  • Location:
BrazilReference: 2025-121541
  • Categories
Clinical Monitoring * __vacancyopjusttionswidget.opt-Business Area__
ICON Strategic Solutions * __vacancyopjusttionswidget.opt-Remote Working __
Office BasedTalent Acquisition Team Lead
  • Icon Strategic Solutions
EmailSend me a messageFirst Name*Last Name*()\[\]\.,;:\s@"]+(\.[^()\\[\]\\.,;:\s@"]+)*)|(".+"))@((\[[0-9]{1,3}\.[0-9]{1,3}\.[0-9]{1,3}\.[0-9]{1,3}])|(([a-zA-Z\-0-9]+\.)+[a-zA-Z]{2,}))$" data-required="true" id="emailinput" maxlength="256" name="emailinput" placeholder="Email address" type="text">Email address*Enquiry*About the roleAs a Clinical Trial Manager (Contracts & Payments) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:
  • Plan and manage all aspects of contracts and payments in the clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
  • Bachelor's degree.
  • Previous experience in site payments and contract negotiation within clinical research in CROs or pharma companies.
  • Demonstrated ability to drive the clinical deliverables of a study.
  • Leadership skills.
  • Advanced English level.
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/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. 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, colour, 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-accommodationsInterested 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.Share:ICON and youImpactful work. Meaningful careers. Quality rewards.At ICON, our employees are our greatest strength. That's why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential.List #1Day in the lifeTeaser labelContent typePublish date08/29/2023SummaryTo excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares herTeaser labelBrazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.Teaser labelContent typePublish date05/23/2023SummaryHow to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to excellTeaser labelSenior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.Teaser labelContent typePublish date04/05/2023SummarySenior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?Teaser labelSenior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.bySuzaita HipolitobySuzaita HipolitoSimilar jobs at ICONSalaryLocationWuhanDepartmentClinical MonitoringLocationWuhanRemote WorkingOffice BasedBusiness AreaICON Strategic SolutionsJob CategoriesClinical MonitoringJob TypePermanentDescriptionAs a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Reference2025-122092Expiry date01/01/0001AuthorAuthorSalaryLocationKorea, SouthDepartmentClinical MonitoringLocationSouth KoreaSeoulRemote WorkingHome-BasedBusiness AreaICON Strategic SolutionsJob CategoriesClinical MonitoringJob TypePermanentDescriptionOncology (Sr.)CRA II, Home-Based, South Korea As a (CRA II/SCRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You wilReference2025-121487Expiry date01/01/0001AuthorAuthorSalaryLocationArgentinaDepartmentClinical MonitoringLocationArgentinaRemote WorkingHome-BasedBusiness AreaICON Strategic SolutionsJob CategoriesClinical MonitoringJob TypePermanentDescriptionThe Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with thReference2025-122023Expiry date01/01/0001AuthorAuthorSalaryLocationBrazilDepartmentClinical MonitoringLocationBrazilRemote WorkingHome-BasedBusiness AreaICON Strategic SolutionsJob CategoriesClinical MonitoringJob TypePermanentDescriptionA Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. 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