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  • 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

  • Submitting regulatory documents to IRB and Sponsor. Submitting the clinical study agreement to organization for review. Attending investigator meeting(s). Developing a preliminary budget and verify all costs. Helping Pl negotiate the study budget direct cost with sponsor to cover all costs (F&A

  • Submitting regulatory documents to IRB and Sponsor. Submitting the clinical study agreement to organization for review. Attending investigator meeting(s). Developing a preliminary budget and verify all costs. Helping Pl negotiate the study budget direct cost with sponsor to cover all costs (F&A

  • Submitting regulatory documents to IRB and Sponsor. Submitting the clinical study agreement to organization for review. Attending investigator meeting(s). Developing a preliminary budget and verify all costs. Helping Pl negotiate the study budget direct cost with sponsor to cover all costs (F&A

  • Submitting regulatory documents to IRB and Sponsor. Submitting the clinical study agreement to organization for review. Attending investigator meeting(s). Developing a preliminary budget and verify all costs. Helping Pl negotiate the study budget direct cost with sponsor to cover all costs (F&A

  • 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 ...

  • Should have knowledge of GCP, Protocol, Safety Reporting, maintenance of essential documents & regulatory documents such as Ethics Committee submission and other regulatory requirements Coordinating Ethics Committee submission, approval and queries Assist in the process of administering the informed consent to potential patients Schedule subject visits as per the protocol to ensure maximal subject ...

  • 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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