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  • dept., payments to vendors, confirmation of payment receipt by vendors and Payment tracking sheet project-wise. To support Medical writing team in search of product specific with defined therapeutic indication published study literatures. To support in traveling to Clinical Study sites, if required Work Experience in Clinical Research Industry of 2 years or more. Willingness to travel at least 10-12 days ...

  • Responsible for review or approval of IP release packages k) Negotiate and manage the budget and payments for investigative sites, CRO and other third party vendors, if applicable l) Write or contribute to preparation of clinical protocols, amendments, informed consent forms, study guides, case report

  • head as appropriate; and participate in and support efforts to develop and implement process/system improvements. To provide clinical research expertise in support to other departments and line functions. Contributes in preparation and implementation of project specific training programs and training materials

  • head as appropriate; and participate in and support efforts to develop and implement process/system improvements. To provide clinical research expertise in support to other departments and line functions. Contributes in preparation and implementation of project specific training programs and training materials

  • head as appropriate; and participate in and support efforts to develop and implement process/system improvements. To provide clinical research expertise in support to other departments and line functions. Contributes in preparation and implementation of project specific training programs and training materials

  • head as appropriate; and participate in and support efforts to develop and implement process/system improvements. To provide clinical research expertise in support to other departments and line functions. Contributes in preparation and implementation of project specific training programs and training materials

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

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