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IQVIA
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Amsterdam,
Netherlands
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interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes ... truly patient-centric
Responsibilities
As a Consultant you will be responsible for
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IQVIA
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Madrid,
Spain
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interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes ... truly patient-centric
Responsibilities
As a Consultant you will be responsible for
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IQVIA
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Bucuresti,
Romania
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Budapest,
Hungary
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Zagreb,
Croatia
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Lisbon,
Portugal
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Sofia,
Bulgaria
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Riga,
Latvia
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Bratislava,
Slovakia
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Belgrade,
Serbia
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internal consultant to pharmacovigilance case processing teams
Representing safety and clinical data ... evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to
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IQVIA
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Bucharest,
Romania
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IQVIA is looking for talented and passionate applicants at the Consultant level to join our Consulting team in Bucharest
As an consultant you will be involved in the development
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IQVIA
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Amsterdam,
Netherlands
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for an enthusiastic Consultant Real-World Evidence and Medical Affairs with a scientific ... are recruiting a consultant to be based in Amsterdam with the objective to contribute to the
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IQVIA
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Singapore
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As a Consultant at IQVIA, you will be responsible for the development & delivery of consulting ... consultant with at least 3 years of experience in Tier 1 or 5 years of experience in Tier 2 consulting firms
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IQVIA
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Wilayah Persekutuan Kuala Lumpur,
Malaysia
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As a Consultant at IQVIA, you will be responsible for the development & delivery of consulting ... consultant with at least 3 years of experience in Tier 1 or 5 years of experience in Tier 2 consulting firms
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IQVIA
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Philippines
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As a Consultant at IQVIA, you will be responsible for the development & delivery of consulting ... consultant with at least 3 years of experience in Tier 1 or 5 years of experience in Tier 2 consulting firms
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IQVIA
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Jakarta,
Indonesia
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As a Consultant at IQVIA, you will be responsible for the development & delivery of consulting ... consultant with at least 3 years of experience in Tier 1 or 5 years of experience in Tier 2 consulting firms
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IQVIA
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Bangkok,
Thailand
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As a Consultant at IQVIA, you will be responsible for the development & delivery of consulting ... consultant with at least 3 years of experience in Tier 1 or 5 years of experience in Tier 2 consulting firms
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IQVIA
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Athens,
Greece
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of statistical methodology to clinical trials.
Assist the Director in strategic planning and ... preparing integrated clinical and statistical reports.
Assist the Director in proposal development
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IQVIA
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London,
United Kingdom
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rich in development and growth.
Role & Responsibilities
As an Associate Consultant ... Consultant should have:**
Minimum of 1-3 years professional experience in strategy consulting, M&A
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IQVIA
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Paris,
France
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rich in development and growth.
Role & Responsibilities
As an Associate Consultant ... Consultant should have:**
Minimum of 1-3 years professional experience in strategy consulting, M&A
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IQVIA
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Warsaw,
Poland
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IQVIA is looking for talented and passionate applicants at the Consultant level to join our Consulting Team in Warsaw .
As a Consultant you will be involved in the development
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IQVIA
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Tallinn,
Estonia
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join us as a Consultant to support our Analytics Solutions team in the Nordics.
This role sits ... Consultant, you will be supporting projects for clients in the Nordics. Consultants are responsible for
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IQVIA
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Bloemfontein,
South Africa
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reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical ... consultant for any medical support for pharmacovigilance operations.**
**This role can be conducted
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IQVIA
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Bellville,
South Africa
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reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical ... consultant for any medical support for pharmacovigilance operations.**
**This role can be conducted
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IQVIA
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Centurion,
South Africa
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reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical ... consultant for any medical support for pharmacovigilance operations.**
**This role can be conducted
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IQVIA
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Wayne, Pennsylvania
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*Consultant(e) principal(e), épidémiologie et sécurité des médicaments, données probantes du monde ... sont à prévoir. *_Le(a) consultant(e) principal(e) est explicitement reconnu(e) comme un membre
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IQVIA
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Parsippany, New Jersey
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*Consultant(e) principal(e), épidémiologie et sécurité des médicaments, données probantes du monde ... sont à prévoir. *_Le(a) consultant(e) principal(e) est explicitement reconnu(e) comme un membre
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IQVIA
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Boston, Massachusetts
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*Consultant(e) principal(e), épidémiologie et sécurité des médicaments, données probantes du monde ... sont à prévoir. *_Le(a) consultant(e) principal(e) est explicitement reconnu(e) comme un membre
...
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IQVIA
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Durham, North Carolina
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*Consultant(e) principal(e), épidémiologie et sécurité des médicaments, données probantes du monde ... sont à prévoir. *_Le(a) consultant(e) principal(e) est explicitement reconnu(e) comme un membre
...
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IQVIA
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New York City, New York
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*Consultant(e) principal(e), épidémiologie et sécurité des médicaments, données probantes du monde ... sont à prévoir. *_Le(a) consultant(e) principal(e) est explicitement reconnu(e) comme un membre
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