משרות נוספות בתחום: מחקר ופיתוח , ניהול פרוייקטים
Manager, Clinical Trial optimization and planning
  • כפר יונה, נתניה, תל מונד
  • משרה מלאה
  • לא צוין שכר
תיאור המשרה:
Lead the evaluation and assessment of the protocol related to optimization initiatives for clinical trial success, which may include but not limited to population evaluation, eligibility criteria, burden of study, etc. Work in collaboration with internal and external functions to ensure efficient processes are being planned, agreed, and executed.
Lead cross functional team meeting including internal Teva teams (operations, clinical development, procurement, health economics and outcomes research, finance etc.) and external suppliers/vendors (CRO, others) through early engagement process to support the insight generation for the program and protocol development
Support TOPS Lead on overall strategy for operational and planning processes to bring innovative or creative approaches, optimized and efficient processes to other/new early project initiatives, for example decentralized strategy.
Working with TOPS Lead to re-evaluate methodologies in the areas of optimization and planning including monitoring the marketplace for new vendors, redefining internal processes by gaining supportive information from industry benchmark and competitive intelligence.
Strong ability to transition analytical outputs to presentation format and deliver the presentation to multi-level functions and teams.
Identifies and aligns with the Teva values, work respectfully, knowledgeably, and effectively with all nationalities in a global environment.
Ensure timely, efficient and high quality deliverables in all projects.
דרישות המשרה:
Bachelors or higher degree in Science, Industrial Engineering, or equivalent combination of education and related work experience
At least 2-3 years’ experience as a project manager in Clinical trial planning/feasibility departments, study start up team, study manager or equivalent in other sponsors, CRO or relevant vendors.
Knowledge of standard Windows programs (Word, Power Point, Outlook etc.).
Ability to effectively interact with and influence others without direct reporting relationships
Experience in setting new methodologies and processes in clinical trials related organizations
ICH-GCP
A proven knowledge in clinical trials and clinical development processes
Understanding of clinical data and pharmaceutical development
Strong written and verbal English
Strong resources management and project management skills
מעבר למשרות דומות בתחומים:
משרה מספר 9189610
metapel
על החברה:
טבע תעשיות פרמצבטיות
גודל חברה: 1001-5000
תעשייה: תרופות
טבע תעשיות פרמצבטיות בע"מ
המשרות באתר מיועדות לנשים וגברים כאחד