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43 jobs found for Biotech Clinical Laboratory

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  • 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 ...

  • 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

  • email, fax,etc.) with subjects, sponsor, monitor and other site study personnel, including: o Ethics Committee o Sponsor o Research Accounting o Laboratories Completing case report forms (CRF) for Pl review and approval. Helping study monitors with CRA corrections Maintaining study- specific supplies ...

  • for developing strong motivated team. 13. Vacancy management. 14. To develop the skills of the team members. 15. To keep the moral high of all team members. Salary: Not Disclosed by Recruiter Industry:Pharma / Biotech / Clinical Research Functional Area:Sales, Retail, Business Development Role Category:Retail

  • for developing strong motivated team. 13. Vacancy management. 14. To develop the skills of the team members. 15. To keep the moral high of all team members. Salary: Not Disclosed by Recruiter Industry:Pharma / Biotech / Clinical Research Functional Area:Sales, Retail, Business Development Role Category:Retail

  • for developing strong motivated team. 13. Vacancy management. 14. To develop the skills of the team members. 15. To keep the moral high of all team members. Salary: Not Disclosed by Recruiter Industry:Pharma / Biotech / Clinical Research Functional Area:Sales, Retail, Business Development Role Category:Retail

  • for developing strong motivated team. 13. Vacancy management. 14. To develop the skills of the team members. 15. To keep the moral high of all team members. Salary: Not Disclosed by Recruiter Industry:Pharma / Biotech / Clinical Research Functional Area:Sales, Retail, Business Development Role Category:Retail

  • activities including MedDRA upgrade, change request initiation. 6. Responsible for preparation and review of department SOPs. 7. Responsible to provide pharmacovigilance training. 8. Assist in Clinical trial activities related to safety issues. 9. Assist in quality management activities ...

  • activities including MedDRA upgrade, change request initiation. 6. Responsible for preparation and review of department SOPs. 7. Responsible to provide pharmacovigilance training. 8. Assist in Clinical trial activities related to safety issues. 9. Assist in quality management activities ...

  • activities including MedDRA upgrade, change request initiation. 6. Responsible for preparation and review of department SOPs. 7. Responsible to provide pharmacovigilance training. 8. Assist in Clinical trial activities related to safety issues. 9. Assist in quality management activities ...

  • Coordination between medical services and axillary and ancillary services. Recruitment and formulation of roster for RMO's. Managing Clinical Nutrition, Biomedical Engineering, Quality, Physiotherapy, Radiology, Laboratory. Handling billing issues ...

  • Coordination between medical services and axillary and ancillary services. Recruitment and formulation of roster for RMO's. Managing Clinical Nutrition, Biomedical Engineering, Quality, Physiotherapy, Radiology, Laboratory. Handling billing issues ...

  • Coordination between medical services and axillary and ancillary services. Recruitment and formulation of roster for RMO's. Managing Clinical Nutrition, Biomedical Engineering, Quality, Physiotherapy, Radiology, Laboratory. Handling billing issues ...

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