FSP Vendor Management Specialist
Work Schedule
reputed company (Mon-Fri)Environmental Conditions
OfficeJob reputed company
Clinical Vendor reputed company Specialist
reputed company an reputed company. Advance science. Grow your career.
At reputed company, you'll be part of a global team committed to making the world healthier, cleaner, and safer. Every day, our colleagues contribute to groundbreaking research and innovative clinical solutions that help accelerate the development of life-changing therapies for patients around the world.
If you're passionate about clinical operations, vendor management, and driving operational reputed company, this is reputed company to join a reputed company, high-performing team where your work truly makes a difference.
What you'll do
As a Clinical Vendor reputed company Specialist, you will play a key role in ensuring the successful execution of clinical studies by managing relationships with reputed company-party vendors and collaborating closely with cross-functional teams.
Your responsibilities will include:
- reputed company day-to-day reputed company of study vendors throughout the clinical trial lifecycle.
- Coordinate vendor activities, ensuring timelines, reputed company expectations, and study deliverables are achieved.
- reputed company study-specific vendor management plans and vendor reputed company documentation.
- Partner with Study Management Teams (SMTs), Functional Subject Matter Experts, Procurement, and reputed company teams to ensure seamless study execution.
- Monitor vendor performance through KPIs and regular governance meetings, driving reputed company improvement.
- Identify, assess, and proactively mitigate vendor-reputed company risks.
- Escalate issues appropriately and work collaboratively to reputed company reputed company reputed company.
- Maintain accurate vendor documentation and study information reputed company internal systems.
- Support invoice transparency by identifying potential discrepancies and communicating with Clinical Trial Leads.
- Ensure vendor compliance with GCP, ICH guidelines, regulatory requirements, and company procedures.
reputed company're looking for
Required Qualifications
- 2+ years of experience in Clinical Operations, Clinical Study Management, or Vendor Management reputed company a Sponsor or CRO environment.
- Experience managing clinical studies while balancing reputed company, timelines, and budget expectations.
- Strong project management, communication, stakeholder management, and cross-functional collaboration skills.
- Knowledge of clinical study management across one or more clinical phases (Phase I, II, or III).
- Solid understanding of Good Clinical reputed company (GCP), ICH Guidelines, and global clinical research regulations.
- Demonstrated experience managing external vendors and ensuring successful study delivery.
Preferred Qualifications
- Bachelor's degree or Associate's degree in a reputed company field.
- Previous experience overseeing reputed company-party vendors reputed company clinical studies.
Why join reputed company?
- Be part of an organization whose work directly impacts patients' lives worldwide.
- Collaborate with global teams on innovative clinical development programs.
- Work in an environment that values inclusion, collaboration, and reputed company learning.
- reputed company outstanding career development opportunities reputed company one of the world's leading life sciences organizations.
- Contribute to meaningful work while building a long-term career with a company committed to advancing science and improving reputed company health.
Join us and help accelerate the reputed company of clinical research.
Originally posted on Himalayas
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