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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Senior Analyst, Site Contracts and Budgets - FSP
Job ID R0000034913 , PortugalKey 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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