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JOB SUMMARY The position is responsible for performing medical review of Individual Case Safety Reports (ICSRs),conducting medical assessement of all safety related data and ensuring medical accuracy...
standardoperatingprocedures musicmaking medicalreview adverseevents caseprocessing drugdevelopment workinstructions professionalliability pv sop psurs meddra clinical reporting hospitals databases edical
Essential Duties and Responsibilities:
As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer
SALARY: upto 6 lacs VACANCIES: 1 QUALIFICATION: MBBS MALE/FEMALE: both EXPERIENCE: above 3 years JOB DETAILS ...
research hplc chemistry validation api research development musicmaking dataintegrity adverseevents datamonitoring informedconsent clinicalresearch it sop dcgi sound ethics agency inform ecJob Description JOB DESCRIPTION/ RESPONSIBILITIES: The LT will report administratively, on a day-to-day basisto theDirector and Head of the concerned TB Laband shall functionally be under the direct...
biochemistry sams hr control science agency mis lc medical tests dst payroll pathology hematology microbiology tandardoperatingprocedures adverseevents qualitycontrol annualreports infectioncontrolSR. DRUG SAFETY ASSOCIATE - As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to ...
caseprocessing pharmacovigilance safety case dataentry drugsafety adverseevents trackingsystems clinicalresearch processimprovement dsa mss icon argus pharma medical research egulat yrequirements acle buEssential Duties and Responsibilities: As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prod
Essential Duties and Responsibilities:
As a Medical Reviewer
Essential Duties and Responsibilities:
As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
safety case drugsafety gvp lifesciences teammanagement clinicaltrials ep ting policiesprocedures peoplemanagementskills stronginterpersonalskills lifecycle globalhealth medicalreview adverseeventsTeam Lead PV Job Description Team Lead JOB Role: Pharmacovigilance Track all adverse event reports received and completed Review and assess all source documents, and compile data in an adverse event...
databases filing pharma genomics adverseevents database pv 10key biomarkers phoneetiquette fax lifesciences drugdiscovery dataentry filemanagement pharmacovigilance spreadsheets copying officeequipment ultilinephoneOverall site management of clinical trialsensuring that projects are progressing according to contract and defined quality standards, Protocol, SOPs, GCP and other applicable guidelines to fulfill loc...
site safety gcp documentation itemonitoring qualitymanagementsystem backoffice siteinitiation riskanalysis qualitystandards humanrights clinicalresearch sitevisits adverseevents sitemanagementEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prodEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
safety case drugsafety gvp lifesciences teammanagement clinicaltrials ep ting policiesprocedures peoplemanagementskills stronginterpersonalskills lifecycle globalhealth medicalreview adverseeventsPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorPrinicipal Investigator Biopeople India Job details Job Details Prinicipal Investigator Description : Review of Study Protocol, Informed Consent Form and CRF, for BA/ BE studies with a focus on pro...
adverseevents informedconsent screening supervision rinicipalInvestigatorOverall site management of clinical trialsensuring that projects are progressing according to contract and defined quality standards, Protocol, SOPs, GCP and other applicable guidelines to fulfill loc...
site safety gcp documentation itemonitoring qualitymanagementsystem backoffice siteinitiation riskanalysis qualitystandards humanrights clinicalresearch sitevisits adverseevents sitemanagementEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials , spontaneous and solicited reports Det...
safety case drugsafety gvp lifesciences teammanagement clinicaltrials ep ting policiesprocedures peoplemanagementskills stronginterpersonalskills lifecycle globalhealth medicalreview adverseeventsEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prodEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
safety case drugsafety gvp lifesciences teammanagement clinicaltrials ep ting policiesprocedures peoplemanagementskills stronginterpersonalskills lifecycle globalhealth medicalreview adverseeventsJOB DESCRIPTION/ RESPONSIBILITIES: The LT will report administratively, on a day-to-day basis to the Director and Head of the concerned TB Lab and shall functionally be under the direct supervision o...
microbiology pathology biochemistry dst lc mis hematology sam nnualreports adverseevents communicationskills qualitycontrol writtencommunication standardoperatingprocedures infectioncontrol teamorientationJob Description JOB DESCRIPTION/ RESPONSIBILITIES: The LT will report administratively, on a day-to-day basisto theDirector and Head of the concerned TB Laband shall functionally be under the direct...
biochemistry sams hr control science agency mis lc medical tests dst payroll pathology hematology microbiology tandardoperatingprocedures adverseevents qualitycontrol annualreports infectioncontrolEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prodSR. DRUG SAFETY ASSOCIATE - As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to ...
caseprocessing pharmacovigilance safety case dataentry drugsafety adverseevents trackingsystems clinicalresearch processimprovement dsa mss icon argus pharma medical research egulat yrequirements acle buPURPOSE OF THE ROLE
Vacancy for Data Analyst Designation: Subject Matter Expert -Data Analyst Work Location: Coimbatore Notice: 30 days / Immediate Joiner Package: 5.5 LPA Experience: 1 to 4 Years can apply...
fax reporting sql ataanalysis adverseevents communicationskills microsoftexcel customerrelationsPURPOSE OF THE ROLE
Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
stronginterpersonalskills lifecycle drugsafety lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures productp tfolio customerhandlEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prodAnalyze, design develop, troubleshoot and debug software programs for commercial or end user applications. Writes code, completes programming and performs testing and debugging of applications. As a m...
unixshellscripting argussafety adverseevents shellscripting automationtools operatingsystems softwareengineering microsofttechnologies applicationdeployment cledatabase netw ktopology
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
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