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Senior Analyst, Site Contracts and Budgets - FSP

Primary Location: Portugal, Remote Job ID R0000034913 Category Clinical Trials
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About this Role

Key Accountabilities
Oversight of activities

  • Negotiate and maintain Clinical Trials Agreements (CTA), site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable contracts 
  • As required, oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols 
  • Ensures compliance of contracts with Fair Market Value (FMV) principles and guidelines. 
  • Track contract progress, complete required follow-ups and coordinate the timely completion of clinical sites contracts 
  • Oversee CRO and Functional Service Provider activities in regards to site CDAs 
  • Develop, maintain, and analyze tools and systems (spreadsheets, Smartsheet, databases, etc.) to manage contract lifecycle from initiation through contract execution, and build internal metadata to support accurate reporting 
  • Negotiate and maintain Clinical Trials Agreements (CTA), site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable contracts 
  • As required, oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols 
  • Ensures compliance of contracts with Fair Market Value (FMV) principles and guidelines. 
  • Track contract progress, complete required follow-ups and coordinate the timely completion of clinical sites contracts 
  • Oversee CRO and Functional Service Provider activities in regards to site CDAs 
  • Develop, maintain, and analyze tools and systems (spreadsheets, Smartsheet, databases, etc.) to manage contract lifecycle from initiation through contract execution, and build internal metadata to support accurate reporting 
  • Provide guidance and direction to new clinical operations and/or outsourcing team members and R&D teams on site contracts & budgets processes 
  • Provide accurate progress updates to Clinical Operations teams on all outstanding contracts and budgets 
  •  Complete required quality checks of appropriate documents and records for completeness and accuracy and ensure adherence to department guidelines/templates; collate quality issues for reporting to team leads 
  • Assist management with process improvement projects 
  • Coordinate and arrange meetings, prepare agendas, and meeting planning 
  • Submit purchase requisitions, where needed, through SAP systems 
  • Support the development and maintenance of guidelines, training programs, policies and procedures related to clinical trial contracts and budget. 
  • Support the Director and team in the management of other day-to-day activities related to clinical contracts and budgets as requested 

Collaborative relationships

  • Collaborate and coordinate with cross-functional teams; R&D, Legal, Compliance, Procurement and Finance in executing contracts 

Compliance with Parexel standards 

  • Complies with required training curriculum  
  • Completes timesheets accurately as required  
  • Submits expense reports as required  
  • Updates CV as required  
  • Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements  

Skills:

  • Excellent verbal, written and interpersonal communication skills in a dynamic and growing organization 
  • Proficient with Excel and PowerPoint 
  • Strong interest in learning more about contracts and budgeting in support of Sponsor clinical trials 
  • Ability to prioritize and manage multiple tasks simultaneously 
  • Some limited travel may be required 

Knowledge and Experience:  

  • Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety 
  • Willingness to learn international clinical pharmaceutical standards, ICH/GCP guidelines and regulatory compliance issues 
  • This position can be staffed also at Senior level based on years of experience in the pharmaceutical or biotechnology industry in clinical site contracts and/or outsourcing management 
  • Analyst, Site Contracts & Budgets level position require 1-3 years of relevant experience as assessed by the client
  • Senior Analyst, Site Contracts & Budgets level position require 3-5 years of relevant experience as assessed by the client

Education:

  • Educated to degree level or equivalent 


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