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Clinical Vendor Manager - Central Labs

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 
United Kingdom

Offer summary

Qualifications:

Bachelor’s degree or equivalent required, 3+ years’ experience with Central laboratories, Excellent knowledge of clinical operations, Vendor management expertise.

Key responsabilities:

  • Accountable for vendor service delivery
  • Review and refine protocol specifications
  • Ensure timely study start-up process
  • Maintain vendor risk maps and contingency plans
Parexel logo
Parexel XLarge http://www.parexel.com
10001 Employees
About Parexel
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is currently seeking an experienced clinical research professional to join us, you be assigned to one of our key sponsors in the region, as a Vendor Stat Up Manager assigned to the Central Labs category.

Working as a Vendor Start Up Manager role, you will be independently accountable for flawless and accelerated vendor service delivery at the trial start-up phase whilst supporting the implementation of defined category strategies and service standardization. This role proactively assesses risk and concludes contingency plans to de-risk study startup.

Some specifics about this advertised role

  • Dedicated to one client.

  • Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol

  • Ensures changes to protocol or study designs are consistently shared with vendors and incorporated into supplier budgets, timelines, and specifications. Supports amendment of vendor contracts with Procurement team

  • Optimizing a frontloaded and timely study start-up process in support of a timely vendor database-go-live

  • Vendor service excellence at study level, ensures vendors meet quality and service level standards in their service delivery for the trial

  • Pro-actively creates and maintains vendor related risk maps with contingency plan for documentation in Facilitated Issue and Risk Surveillance Tool

Here are a few requirements specific to this advertised role.

  • Bachelor’s degree or equivalent degree is required, with advanced degree preferred.
  • 3+ years’ experience working with Central laboratories and specialty labs.
  • Excellent knowledge of the clinical operation processes and vendor management

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Risk AnalysisSurgical ProceduresVendor ManagementProtocol AnalysisContract LawService Level ObjectivesContingency PlanningLaboratory Experience

Other Skills

  • Teamwork
  • Communication
  • Problem Solving
Are you interested?

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