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3369 jobs found for Senior Manager Clinical Research

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  • To perform the Site Monitoring Visits for in-house projects To perform the Co-Visits for outsourced projects To prepare the study budget in consultation with line manager/business development team for the assigned projects. To negotiate with Investigators for sites budget and execution of CTAs To prepare

  • To perform the Site Monitoring Visits for in-house projects To perform the Co-Visits for outsourced projects To prepare the study budget in consultation with line manager/business development team for the assigned projects. To negotiate with Investigators for sites budget and execution of CTAs To prepare

  • To perform the Site Monitoring Visits for in-house projects To perform the Co-Visits for outsourced projects To prepare the study budget in consultation with line manager/business development team for the assigned projects. To negotiate with Investigators for sites budget and execution of CTAs To prepare

  • To perform the Site Monitoring Visits for in-house projects To perform the Co-Visits for outsourced projects To prepare the study budget in consultation with line manager/business development team for the assigned projects. To negotiate with Investigators for sites budget and execution of CTAs To prepare

  • Job role will typically involve- a) Oversee performance of CROs, third party vendors, and field CRAs including co-monitoring, to ensure compliance with study protocol and in accordance with scope of work; identify areas of concern and escalate to Director or CRO as appropriate b) Perform clinical

  • package (including SMF). Co-ordination & tracking for dispatch, maintenance & retention/disposition of Clinical trial supplies (IP & non-IP) as per SOP & study requirement. Ensure that the sites have the required clinical supplies for proper conduct of the study. Prepare & finalize study specific

  • clinical supplies for proper conduct of the study. Perform site visits i.e. site selection, initiation, monitoring & close out, prepare and submit follow up letter, visit reports as per SOP & monitoring plan Perform SDV & CRF review as per the monitoring plan Review key study quality metrics (e.g ...

  • clinical supplies for proper conduct of the study. Perform site visits i.e. site selection, initiation, monitoring & close out, prepare and submit follow up letter, visit reports as per SOP & monitoring plan Perform SDV & CRF review as per the monitoring plan Review key study quality metrics (e.g ...

  • clinical supplies for proper conduct of the study. Perform site visits i.e. site selection, initiation, monitoring & close out, prepare and submit follow up letter, visit reports as per SOP & monitoring plan Perform SDV & CRF review as per the monitoring plan Review key study quality metrics (e.g ...

  • clinical supplies for proper conduct of the study. Perform site visits i.e. site selection, initiation, monitoring & close out, prepare and submit follow up letter, visit reports as per SOP & monitoring plan Perform SDV & CRF review as per the monitoring plan Review key study quality metrics (e.g ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

  • Clinnovo Provides training,internships,diploma and hands of experience in Clinical research,SAS,CDM. Clinnovo offers above aspects in Clinical Research Clinical Data Management SAS Pharmacovigilance Clinical trial management,drug regulatory affairs Needed to be passion about science. 1. Bsc, Msc,B.E bio,M tech Bio,Phd 2. Good % aggregate in school and university 3. Excellent verbal and written ...

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