Senior Site Contracts Leader (COM F) - FSP
at Parexel
Home Office, Iowa, Czech -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 13 Feb, 2025 | Not Specified | 14 Nov, 2024 | 5 year(s) or above | Clinical Research,Completion,Financial Forecasting,Negotiation,Life Science,Oversight | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
EXPERIENCE REQUIRED:
- 5 years in clinical research or combined experience in Clinical Research and Finance/Business.
- Experience in the development, negotiation, and completion of clinical trial agreements.
- Experience in oversight and tracking of clinical research‐related payments
- Experience in payment reconciliation at study close‐out.
- Experience in financial forecasting.
- Education: Bachelor’s degree in business finance/administration, life science, or equivalent healthcare-related experience.
Responsibilities:
ABOUT THIS ROLE
Join the Parexel FSP Team as a Senior Site Contracts Leader!
Are you ready to make a real impact on the success of our clinical trials? We’re seeking a talented individual to play a crucial role in ensuring performance and compliance with assigned protocols. As a Site Contracts Leader, you’ll navigate the complexities of ICH/GCP regulations, oversee budget and finance aspects, and drive excellence to deliver results.
Dedicated to one sponsor, a global pharmaceutical company that leads the way in discovering and developing innovative health solutions that help prevent and treat diseases in animals and people.
Our sponsor has a long history of excellence in research and has delivered medicines, vaccines, and other health solutions for some of the world’s most difficult diseases.
RESPONSIBILITIES:
- Budget Ownership: Manage country and site budgets, including development, negotiation, and completion of Clinical Trial Research Agreements (CTRA).
- Financial Oversight: Track clinical research-related payments, reconcile payments at study closeout, and maintain financial systems. Collaborate with Sr. COM and other roles for financial forecasting.
- Protocol Management: Ensure country deliverables, timelines, and results align with commitments. Maintain quality and compliance with assigned protocols.
- Local SOP Development: Contribute to developing local Standard Operating Procedures (SOPs) and oversee Clinical Trial Coordinators (CTCs) as applicable.
- Collaboration: Coordinate with CRM, CTC, CRA, and other relevant teams (Finance and Legal) to obtain country deliverables for submissions, budgets, CTRAs, and local milestones. Align country timelines with headquarters for assigned protocols.
- Vendor Support: Provide oversight and support to local vendors as needed.
- Financial Compliance: Oversee local financial compliance, ensuring adherence to budget targets and payment timelines.
- Influence and Partnership: Work internally with GCTO country operations, finance, legal, and regional teams, as well as externally with vendors and sites. Influence investigators and external partners.
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Business finance/administration life science or equivalent healthcare-related experience
Proficient
1
Home Office, Czech