Medical Clinical Trial Operations Specialist (m/f/d)

☞ Universal-Job

View: 150

Update day: 10-04-2024

Location: Baar Zug ZG

Category: Pharmacist / Pharmaceutical representatives

Industry:

Job type: 100%, Intérim, Temps de travail : 90-100%

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Job content

The Manager, MRO provides operational expertise in and oversight of the execution of post-drug approval research. This position supports the generation of post-approval data and medical evidence in the disease areas that our client addresses. In this role, you will act as an operational partner in driving data generation program execution. Working across late-stage development and marketed products, the incumbent will manage the operations for Phase 4 studies, patient registries, outcomes research, and real-world evidence programs. Activities include study planning, start-up, vendor management, site management, tracking and reporting.

Motivation
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!

Firmenprofil
Global Pharma Company.

Spezielles
If you are interested then kindly send your resume to: a.ahanor@universaljob.ch

Erfahrung
- Minimum of 7+ years of clinical research experience with minimum of 5+ years of CRO/Sponsor Project Management - Strong Project Management skills including risk assessment and contingency planning - Demonstrated learning agility - Possess a combination of critical thinking and operational know-how and efficiency

Ausbildung
Minimum of a Bachelor’s degree in a health-related field with clinical research experience

Sprachen
English: Advanced


Arbeitsort
Baar

Arbeitsbeginn
Asap

Vakanz-Nummer
P-13-8070

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Deadline: 25-05-2024

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