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Site Contract Specialist

Role overview

Qualifications

  • Paralegal certification or Associate’s degree
  • At least two years of experience in a professional administrative/business role
  • Fluent in spoken and written Italian and English

Responsibilities

  • Initiate site contact and follow-up for CDA and CTA drafts
  • Administer contract language within sponsor guidelines and work with legal counsel on revisions
  • Facilitate CDA and CTA completion and execution
  • Maintain contract files and CDA and CTA tracking sheets

Key facts

  • Remote from: Spain
  • Fixed term
  • English, Italian

Hard skills

Other skills

  • Communication
  • Teamwork
  • Detail Oriented

About the company

CTI Clinical Trial and Consulting Services logo

CTI Clinical Trial and Consulting Services

Contract Research Organizations (CRO)

CTI Clinical Trial and Consulting Services is a global, privately held, full-service contract research organization (CRO), delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI’s focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare diseases, regenerative medicine/gene therapy, immunology, transplantation, nephrology, hematology/oncology, neurology, infectious diseases, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site that conducts phase I-IV trials. CTI has a passion for helping life-changing therapies succeed in chronically and critically ill patient populations. With clinical trial experience across 6 continents, CTI partners with research sites, patients, and sponsors to fulfill unmet medical needs. CTI is headquartered in Cincinnati, OH, with operations across North America, Europe, Latin America, and Asia-Pacific. For more information visit www.ctifacts.com

Company details

IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

** Please submit your application in English **

What You'll Do:

  • Initiate site contact and follow-up as necessary to turn study confidentiality agreements (CDA) and study clinical trial agreement (CTA) drafts
  • Administer contract language to ensure it remains within approved sponsor guidelines and work with legal counsel on contract revision and negotiation
  • Facilitate CDA and CTA completion and execution
  • Attend internal and external project team meetings and report on CDA and CTA progress
  • Maintain contract files and internal/external CDA and CTA tracking sheets
  • Update CTA status within the internal study start-up module for all assigned studies
  • Assist with contract preparation, review, revision, execution and filing
  • Advise appropriate parties of significant terms (e.g. expiration dates, renewal terms, compliance obligations, etc.)
  • Assist with CDA preparation, review, negotiation, execution and filing.
  • Maintain CDA tracking
  • Maintain CDA archives
  • Process new consultant paperwork and maintain files

What You'll Bring:

  • Paralegal certification or Associate’s degree
  • At least two years of experience in a professional administrative/business role
  • Fluent in spoken and written Italian and English

About CTI

  • Advance Your Career – We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals.
  • Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
  • Make a Lasting Impact – At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.

Important Note

In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.

Please Note

  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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