drjobs Imaging Operations Manager, Clinical Studies

Imaging Operations Manager, Clinical Studies

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1 Vacancy
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Job Location drjobs

London - UK

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Description Summary

Internal job title: Imaging Operations Manager
Location: London (UK) or Dublin (Irland)


As Imaging Operations Manager (IOM) you will be responsible for the operational implementation of the imaging strategy for assigned clinical studies in close collaboration with the Clinical Trial Team (CTT). You may support the full study lifecycle and/or contribute directly to the study sub-team(s).
In this role you will enable a flawless and accelerated vendor service delivery at the trial start-up phase and support implementation of defined category strategies and service standardization. You proactively assess risk and conclude contingency plans to de-risk study startup and milestones.

This position is part of VP&G (Vendor Partnership & Governance) Vendor Alliance Imaging team and reports directly to the Vendor Alliance Lead Associate Director.

It is a hybrid position and requires regular presence on site
#LI-Hybrid



Job Description

Key Responsibilities:

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

  • Contributing to development of Study Specification Worksheet (SSW) to facilitate bid process and selection of Vendors incl. reviewing Quote/Proposal review in collaboration with procurement (and vendor) supporting contract negotiations and budget review

  • Co-ordinating vendor kick-off meeting managing the imaging vendor interface with the study team including leading vendor meetings driving preparation of key documents tracking adherence of critical vendor milestones

  • Ensuring 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 (SSU) process in support of a timely vendor database (DB)-go-live

  • Monitoring vendor service excellence at study level ensuring vendors meet quality and service level standards in their service delivery for the trial

  • Pro-actively creating and maintaining vendor related risk maps with contingency plan for documentation in company tool documenting there also issues identified with vendor oversight / performance implementing and monitoring corrective actions escalating issues if required to the Vendor Alliance Lead (VAL).

  • Supporting the implementation of standards templates tools and processes for vendors at SSU for defined categories in collaboration with the VAL. Driving root cause analysis of supplier performance issues and look for trending supporting practice leaders in improvement projects and learning loops

  • Participating in the onboarding mentoring and training of new staff as applicable to specific category

  • In partnership with the vendor developing site and monitor training material and attend/support training if needed

Minimum Requirements:

  • Advanced degree in science or business with experience in trial vendor management ideally in the category Imaging

  • Fluent English oral and written

  • Solid working experience and excellent knowledge of the clinical operation processes and vendormanagement

  • Excellent knowledge of GxP and ICH regulations

  • Expert knowledge of clinical trial design and mapping to supplier requirements

  • Demonstrated leadership with supplier relationshipservice areasmanagement and/or expert knowledge of specific

  • Demonstrated partnering across divisions with internaland external stakeholders

  • Demonstrated root cause analysis problem solving andsolution generation skills

  • Knowledge of key deliverables that impact green lightmilestones and vendor readiness

  • Experience in outsourcing contracting sourcing of clinical services with Vendor/CROs (RFP RFQcontracting)

Why Novartis

Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:

Some restrictions on flexible working options may apply and will be discussed during interview if applicable

Youll receive:

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook: to Diversity & Inclusion:

Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.

Hiring decisions are only based on the qualification for the position regardless of gender ethnicity religion sexual orientation age and disability.

The law provides for severely disabled / equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you

would like to request this please let us know in advance as a note on your CV.

Adjustments for Applicants with Disabilities:

The law provides for severely disabled / equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you would like to request this please let us know in advance as a note on your CV.

Join our Novartis Network:

If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities join the Novartis Network here:

Desired

Budget Management Clinical Trials Negotiation Skills Process Improvement Project Planning Vendor Management Waterfall Model

Required Experience:

Manager

Employment Type

Full-Time

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