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IQVIA
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Madrid,
Spain
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EMEA external comparator offering lead, you will be responsible for organising our regional efforts to ... European external comparators, in close collaboration with the Global Medical Affairs Product Strategy Lead
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IQVIA
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Madrid,
Spain
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Job Overview
This role applies requires applying technical skills to quality assurance an
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IQVIA
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Madrid,
Spain
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• Manage the allocation of development staff to projects at a sub-regional level, business develo
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IQVIA
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Madrid,
Spain
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mentor to junior members of staff. You may also act as functional lead on medium to large operational ... **
• Contribute knowledge and expertise to or lead assigned deliverables in the field of Safety Publishing, Risk
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IQVIA
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Madrid,
Spain
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Sales Engineering Director
Location: London, UK (Hybrid role)
Additional Locat
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IQVIA
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Madrid,
Spain
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Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
Essential Functions
• Serve ... .
• May conduct data review.
• May write and resolve data clarifications.
• May lead database audit
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IQVIA
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Madrid,
Spain
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use of RIM systems and RIM configuration
• Lead gathering and analysis of regulatory business processes and requirements
• Lead RIM system design and configuration sessions with the clients
• Lead
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IQVIA
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Madrid,
Spain
...
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This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data ... as a CDM project lead; or equivalent combination of education, training and experience
Previous
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IQVIA
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Madrid,
Spain
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Join us on our exciting journey!
Position Purpose
The tasks of the **Data Bas
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IQVIA
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Madrid,
Spain
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environment with Lifecycle safety team members,* *lead by example, provide training and mentoring for less
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IQVIA
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Madrid,
Spain
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; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site ... improvements, issue escalation, workload projections, and provide technical expertise
• Lead direct
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IQVIA
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Madrid,
Spain
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Practice Segment Strategy Lead, Medical Specialties & Healthcare
**Team Overview ... .
Job Summary: Lead segment/domain-specific innovation and technology strategy in the Integrated
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IQVIA
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Madrid,
Spain
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. Perform role of Data Team Lead (DTL).
Essential Functions
• Gather Study Set up requirements ... deliverables in contract/Scope of Work (SOW).
• Support Training of New joiners.
• Lead internal study
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IQVIA
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Madrid,
Spain
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Overview - Associate Principal – Patient Centered Solutions, CNS Practice
IQVIA pro
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IQVIA
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Madrid,
Spain
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maximum ROI.
Lead market data analyses projects and provides recommendations for pay levels and
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IQVIA
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Madrid,
Spain
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Join us on our exciting journey!
IQVIA™ is the leading human data science company focused
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IQVIA
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Madrid,
Spain
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Job Overview
_IQVIA Connected Devices is a service that accelerates trial outcomes by str
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IQVIA
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Madrid,
Spain
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The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory ... and rest of the world.
• Lead Regulatory submission Team Leaders under his/her remit and
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IQVIA
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Madrid,
Spain
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Technology Lead will be responsible for MDM Offering Definition and supervision of all the initiatives
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IQVIA
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Madrid,
Spain
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IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in
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IQVIA
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Madrid,
Spain
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Associate Epidemiology Director
IQVIA Real World Solutions
Home-Ba
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IQVIA
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Madrid,
Spain
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The role-holder will need to be a committed individual, who combines high emotional intelligence and
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IQVIA
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Madrid,
Spain
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Join us on our exciting journey!
Position Purpose
We are looking for a **Cust
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IQVIA
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Madrid,
Spain
...
Join us on our exciting journey!
Position Purpose
We are looking for a **Cust
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IQVIA
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Madrid,
Spain
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Join us o n our exciting journey!
We are looking for a F **resh Graduate Frenc
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IQVIA
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Madrid,
Spain
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Join us on our exciting journey!
Position Purpose:
We are recruiting an awesome team of Nordic language speakers to join us at our Madrid Production Hub office! We are looking
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IQVIA
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Madrid,
Spain
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Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently pr
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IQVIA
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Madrid,
Spain
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Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently pr
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