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Durham, North Carolina
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We are seeking a Decentralized Trial Solutions Manager to join Q2 Solutions, IQVIA’s ... decentralized trial solutions.
What you’ll be doing:
· Lead cross functional teams to
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Durham, North Carolina
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Location: home-based in the U.S. or Canada
Summary: IQVIA is hiring to expand a ... clinical trial data review.
Job responsibilities:
Follow steps to set-up studies and
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Frankfurt,
Germany
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Join IQVIA as a CRA / SrCRA (m/w//d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications
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Netanya,
Israel
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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New Cairo,
Egypt
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Frankfurt,
Germany
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areas.
We currently offer the exciting opportunity to join the team as Local Trial Manager or Senior Local Trial Manager (m/w/d) in full-time and work **home-based
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Vienna,
Austria
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Manager (m/w/d)** in full-time and work home-based throughout Austria . In this role you will be accountable for the operational management of the component of a clinical trial. Furthermore, you
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Parsippany, New Jersey
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site staff and study staff for the protocol. The Medical Monitor will liaise with clinical trial sites ... * required *. **
**Establish relationships with clinical trial sites to discuss protocol questions
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Durham, North Carolina
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site staff and study staff for the protocol. The Medical Monitor will liaise with clinical trial sites ... * required *. **
**Establish relationships with clinical trial sites to discuss protocol questions
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Paris,
France
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Solna,
Sweden
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Vienna,
Austria
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Oslo,
Norway
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Amsterdam,
Netherlands
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Frankfurt,
Germany
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Frankfurt,
Germany
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Neurology.
When you join the IQVIA sponsor-dedicated cFSP team **home-based throughout Germany ... practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International
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Athens,
Greece
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Rome,
Italy
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Riga,
Latvia
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Madrid,
Spain
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Budapest,
Hungary
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Kaunas,
Lithuania
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Belgrade,
Serbia
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Livingston,
United Kingdom
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Bellville,
South Africa
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Lisbon,
Portugal
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Milan,
Italy
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Prague,
Czech Republic
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Kiev,
Ukraine
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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Sofia,
Bulgaria
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Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex
Ability to ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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