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168 jobs found for Clinical Research Internship Manager

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  • Responsible for aggregate safety report submission management in the country(ies), including report scheduling, submissions and submission compliance entries in accordance with Global Safety procedures and health authority requirements. Responsible for ensuring of after-hours coverage

  • Responsible for aggregate safety report submission management in the country(ies), including report scheduling, submissions and submission compliance entries in accordance with Global Safety procedures and health authority requirements. Responsible for ensuring of after-hours coverage

  • Uploading of executed contracts on CBREs contract database Management of CBREs contract database Will be trained on interpretation of relevant clauses in a commercial contract Extraction of relevant information from the executed contracts Review of commercial contracts/legal documentation Legal

  • Uploading of executed contracts on CBREs contract database Management of CBREs contract database Will be trained on interpretation of relevant clauses in a commercial contract Extraction of relevant information from the executed contracts Review of commercial contracts/legal documentation Legal

  • in accordance with the requirements of the Clinical Protocol. Perform database configuration and programming review and approve verification unit testing Collaborate with colleagues during planning & handover meetings regarding project timelines, and project-related issues focusing on capabilities within Data

  • to identify new markets and opportunities. 8. Direction to weak territories & weak brands 9. Engagement with KBLs/KOLs through different academic activities. 10. Key Account Management. 11. Regular CMEs in the zone. 12. Identification & follow up of training needs of M.Rs & Managers and giving them coaching

  • Position:4 Qualification:MD-Pathologist Experience:Min 5 yrs We are looking for an experienced pathologist. The ideal candidate will be knowledgeable in all laboratory and clinical procedures and have an extensive background in pathology. The position will require testing and analyzing samples

  • Position:4 Qualification:MD-Pathologist Experience:Min 5 yrs We are looking for an experienced pathologist. The ideal candidate will be knowledgeable in all laboratory and clinical procedures and have an extensive background in pathology. The position will require testing and analyzing samples

  • Position:4 Qualification:MD-Pathologist Experience:Min 5 yrs We are looking for an experienced pathologist. The ideal candidate will be knowledgeable in all laboratory and clinical procedures and have an extensive background in pathology. The position will require testing and analyzing samples

  • to identify new markets and opportunities. 8. Direction to weak territories & weak brands 9. Engagement with KBLs/KOLs through different academic activities. 10. Key Account Management. 11. Regular CMEs in the zone. 12. Identification & follow up of training needs of M.Rs & Managers and giving them coaching

  • to identify new markets and opportunities. 8. Direction to weak territories & weak brands 9. Engagement with KBLs/KOLs through different academic activities. 10. Key Account Management. 11. Regular CMEs in the zone. 12. Identification & follow up of training needs of M.Rs & Managers and giving them coaching

  • to identify new markets and opportunities. 8. Direction to weak territories & weak brands 9. Engagement with KBLs/KOLs through different academic activities. 10. Key Account Management. 11. Regular CMEs in the zone. 12. Identification & follow up of training needs of M.Rs & Managers and giving them coaching

  • that includes a wide range of therapeutic categories (OSD) and drug Delivery systems. Activity includes Formulation Development, Technology Transfer, Clinical Research, Regulatory Affairs, Intellectual Property, Projects Management etc. Responsible for ideation, review of literature, Patent search ...

  • that includes a wide range of therapeutic categories (OSD) and drug Delivery systems. Activity includes Formulation Development, Technology Transfer, Clinical Research, Regulatory Affairs, Intellectual Property, Projects Management etc. Responsible for ideation, review of literature, Patent search ...

  • Report regularly all matters of significance to the Director and Clinical Director. 5. To be responsible for co-ordinating the weekly High Risk meeting 6. Participate in quality improvement, peer review and research programs. 7. Participate in the lecturing and training of junior medical staff, medical

  • presentations and dashboards as required by management as per defined timelines Close coordination with all stakeholders: all support functions, field team, clinic team and partners Conduct a thorough research and summarize findings about untouched territories and go to market plan Be updated with latest Excellent analytical and logical thinking, Deliver accuracy with reasonable speed, Good command in ...

  • supervision of the Area (Surgical ICU): monitoring (including clinical observation), pain relief, fluid therapy, respiratory therapy, adverse effects which may be related to anesthesia, preoperative medical problems. If required consultation may be taken from Consultant Provide stand by anesthesia / general

  • supervision of the Area (Surgical ICU): monitoring (including clinical observation), pain relief, fluid therapy, respiratory therapy, adverse effects which may be related to anaesthesia, preoperative medical problems. If required consultation may be taken from Consultant Provide stand by anaesthesia / general MBBS + diploma/MD/MS/DNB in anaesthesia

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