CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services
1,001 – 5,000 Employees
BiotechnologyConsultingHealthcare
CTI Clinical Trial and Consulting Services is a contract research organization serving biotechnology and pharmaceutical sponsors throughout the clinical development process. Its work spans clinical trial execution, regulatory strategy, laboratory and bioanalytical services, real-world evidence, and research center management across Phase I–IV studies. CTI brings experience in areas such as rare diseases, cell and gene therapy, oncology, neurology, and transplantation, supporting study design, site management, patient recruitment, monitoring, safety and pharmacovigilance, biometrics, and quality assurance. The company combines integrated trial services with patient-focused research and global regulatory guidance.

Site Contract Specialist – Remote in Poland

Remote, full-time role in Poland supporting confidentiality and clinical trial agreements for CTI Clinical Trial and Consulting Services. The position coordinates contract negotiations, execution, tracking, and regulatory file management.

Description

  • Contact study sites and follow up as needed to convert confidentiality agreement (CDA) and clinical trial agreement (CTA) drafts
  • Manage contract language within approved sponsor guidelines and collaborate with legal counsel on revisions and negotiations
  • Coordinate the completion and execution of CDAs and CTAs
  • Participate in internal and external project meetings and provide updates on CDA and CTA progress
  • Maintain contract files and internal and external CDA and CTA tracking records
  • Update CTA status in the internal study start-up module for assigned studies
  • Support contract preparation, review, revision, execution, and filing
  • Inform relevant stakeholders about key terms, including expiration dates, renewal provisions, and compliance obligations
  • Support CDA preparation, review, negotiation, execution, and filing
  • Maintain CDA tracking records and archives
  • Process new consultant documentation and maintain related files

Requirements

  • Paralegal certification or an associate degree
  • At least two years of experience in a professional administrative or business role
  • Experience with a pharmaceutical company or Clinical Research Organization (CRO) preferred
  • Basic knowledge of medical and pharmaceutical terminology preferred

Benefits

  • Structured mentoring and leadership development courses
  • Tuition reimbursement
  • Dedicated training department
  • Comprehensive health benefits
  • Vacation packages
  • Hybrid work-from-home opportunities
  • Paid parental leave
  • CTI Cares program
  • Support for work-life balance

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