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
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
Requirements:
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
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
This position is open to all candidates.
