-
IQVIA
-
São Paulo,
Brazil
...
members of the team.
RESPONSIBILITIES
Acts as a Clinical Trials Regulatory Manager (CTRM) on complex clinical trial projects/programs and may act as a Regulatory Oversight for a key
...
-
IQVIA
-
Mexico City,
Mexico
...
members of the team.
RESPONSIBILITIES
Acts as a Clinical Trials Regulatory Manager (CTRM) on complex clinical trial projects/programs and may act as a Regulatory Oversight for a key
...
-
IQVIA
-
Buenos Aires,
Argentina
...
members of the team.
RESPONSIBILITIES
Acts as a Clinical Trials Regulatory Manager (CTRM) on complex clinical trial projects/programs and may act as a Regulatory Oversight for a key
...
-
IQVIA
-
Durham, North Carolina
...
Job Overview
Clinical Trial Educator (CTE) Manager manages CTE teams and supports internal stakeholders and sponsors to ensure research teams can optimize clinical trial enrolment. May act
...
-
IQVIA
-
Lima,
Peru
...
Clinical Trial Manager – Sponsor Dedicated.
Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or
...
-
IQVIA
-
Mexico City,
Mexico
...
Clinical Trial Manager – Sponsor Dedicated.
Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or
...
-
IQVIA
-
São Paulo,
Brazil
...
Clinical Trial Manager – Sponsor Dedicated.
Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or
...
-
IQVIA
-
Buenos Aires,
Argentina
...
Clinical Trial Manager – Sponsor Dedicated.
Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or
...
-
IQVIA
-
Santiago,
Chile
...
Clinical Trial Manager – Sponsor Dedicated.
Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or
...
-
IQVIA
-
Brussels,
Belgium
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Tel Aviv,
Israel
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
New Cairo,
Egypt
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Frankfurt,
Germany
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Vienna,
Austria
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Solna,
Sweden
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Paris,
France
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Gothenburg,
Sweden
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Amsterdam,
Netherlands
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Oslo,
Norway
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Ljubljana – Dunajska,
Slovenia
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Lisbon,
Portugal
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Belgrade,
Serbia
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Warsaw,
Poland
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Kiev,
Ukraine
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Istanbul,
Turkey
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Athens,
Greece
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Riga,
Latvia
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Livingston,
United Kingdom
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Reading,
United Kingdom
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
-
IQVIA
-
Kaunas,
Lithuania
...
a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
...
