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Responsibilities
* Senior Safety Physician Come discover what our 25,000+ employees already know: work here matters everywhere. We re a growing and evolving biopharmaceutical industry leader, which...
medical reviewaudio masteringmicrosoft officestandard operating proceduresmusic makingwork instructionsadverse eventsmedical educationdrug developmentcase processing* Safety Physician Come discover what our 25,000+ employees already know: work here matters everywhere. We re a growing and evolving biopharmaceutical industry leader, which means ...
standard operating procedurescarelegislative relationsexcelprofessional liabilitysopcommunication skillsmicrosoft officework instructionsdrug developmentinterpersonal skillsamericans with disabilities actThis role will also have other responsibilities such as reconciliations of adverse drug reports with medical information and other business partners and updating other Pharmacovigilance staff regardin...
businesscasemedical educationargus safetydrug safetyelectronic common technical documentinternal medicinemeddrafamily medicinepsursmedical affairscase processinge2barisgdata entryadverse event reportingpharmacovigilancepsursafetymedical Skill required: Pharmacovigilance - Medical Writing
Designation: Senior Analyst
Qualifications: Master of Pharmacy
* Safety Physician Come discover what our 25,000+ employees already know: work here matters everywhere. We re a growing and evolving biopharmaceutical industry leader, which means y...
standard operating procedurescase processingmicrosoft officeamericans with disabilities actcarelegislative relationsmusic makingprofessional liabilityinterpersonal skillsmedical reviewwork instructionsexcelsopdrug developmentwritten coSkill required: Pharmacovigilance - Pharmaceutical Drug Safety Surveillance Designation: Management Level - Manager Job Location: Benga...
data entrydrug safetyadverse eventsbusiness processsenior managementmeddra codingsetvisitdealsdesignmanualmeddrachecksscienceresearchbusinessmedicalSkill required: Pharmacovigilance - Medical Affairs Designation: Associate Job Location: Bengaluru Qualifications:...
data entryadverse eventsquality controlmedical affairsadvisory boardsbusiness processbusiness solutionsthought leadershipdigital conversionstatements of work sowManager, Drug Safety PhysicianQualificationsMBBS/MD Electronic Common Technical Document ,...
drug safetysafetycasecompliancegvpMedDRAARISgPSURsArgus SafetyPSURE2BMedical AffairsElectronic Common Technical DocumentAdverse Event ReportingPRIMARY RESPONSIBILITIES As a Medical Safety Physician Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regu...
life cycledrug safetylife sciencesglobal healthmedical reviewpatient safetyadverse eventsteam managementclinical trialspeople managementEssential Duties and Responsibilities: As a Medical Reviewer
Essential Duties and Responsibilities: As Quality Check Reviewer
Essential Duties and Responsibilities: As Quality Check Reviewer
PRIMARY RESPONSIBILITIES As a Senior Medical Safety Physician Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determi...
life cycledrug safetylife sciencesglobal healthmedical reviewpatient safetyadverse eventsteam managementclinical trialspeople managementEssential Duties and Responsibilities: As Quality Check Reviewer
The role of the Senior Clinical Data Coder (Sr. CDC) is to manage the performance of clinical data coding activities from database set-up through database lock on assigned projects, commensurate with ...
medical terminology21 cfrclinical datawork effectivelydata managementdata codingms officetime managementclinical trialswritten communicationtechnical skills Skill required: Pharmacovigilance - Medical Writing
Designation: Senior Analyst
Qualifications: Master of Pharmacy
A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Elec...
active directorytroubleshootingenvironmentwindowsslarisk managementclinical trialsdata monitoringtherapeutic areasclinical developmentpersonal developmentJob Purpose: The Drug Safety Associate I, will provide technical and process-related support to drug safety management (clinical trial and post-marketed) and medical monitoring activities, ensuring ...
case processingpharmacovigilancesafetycasedata entryitem response theorystandard operating proceduresdrug safetymusic makinglife sciencesstudy reportssearch strategyquery managementsafety managementROLE RESPONSIBILITIES
Skill required: Pharmacovigilance - Medical Affairs
Designation: Management Level - Associate
Job Location: Bengaluru
The Senior Clinical Data Analyst (SCDA) shall be responsible for data processing activities on a project and shall ensure quality standards according to SOPs and ICH-GCP. Areas of responsibility shall...
deliverybasisbillingcrfdata managementdata entrydata analysisclinical datadata cleaningmedical codingdata processingclinical researchquality standardssae reconciliationmedical terminologySkill required: Pharmacovigilance - Medical Affairs Designation: Management Level - Analyst Qualifications: Bachelor of Aryurvedic Medi...
data entryadverse eventsquality controlmedical affairsadvisory boardsbusiness processbusiness solutionsthought leadershipSkill required: Pharmacovigilance - Pharmaceutical Drug Safety Surveillance Designation: Management Level - Associate Qualifications: B...
data entrydrug safetyadverse eventsbusiness processmeddra codingbasicvisitdealsdesignmanualmeddrastatements of work sowEssential Duties and Responsibilities: As a Medical Reviewer
PRIMARY RESPONSIBILITIES As a Medical Safety Physician Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regu...
life cycledrug safetylife sciencesglobal healthmedical reviewpatient safetyadverse eventsteam managementclinical trialspeople managementSkill required: Pharmacovigilance - Medical Writing Designation: Management Level - New Associate Qualifications: Any Graduation accounts payableaccounts payablereceivableapproval processbudgetingcreditdata entryadverse eventsclinical trialsbusiness process
Drug Safety Physician - Pharmacovigilance
Candidates with experience in Pharmacovigilance ICSR Review for minimum 1- 4 year
Department- Pharmacovigilance
<... drug safetysafetycasecompliancegvppharmacovigilanceMedDRAARISgPSURsArgus SafetyPSURE2BMedical AffairsElectronic Common Technical DocumentAdverse Event ReportingElectronic Common Technical Document eCTD
Responsibilities
Medical review of Aggregate reports. QualificationsMBBS MD 2 - 3 years of PV experience(experience in Aggregate reporting desirable); Experience in safety document or medical writing ...
safetycasedrug safetygvpreportingmedical writingdrawritingpreparationdictionariesMedical CommunicationsPublication PlanningMedical AffairsAbstractsContinuing Medical EducationMedDRAPSURPSURsmedicalEssential Duties and Responsibilities: As Case Intake Member:
Essential Duties and Responsibilities: As Quality Check Reviewer
Essential Duties and Responsibilities: As Quality Check Reviewer
Essential Duties and Responsibilities: As Quality Check Reviewer
Performs medical review of adverse events reported for investigational and marketed products Maintains familiarity with MedDRA, WHO-DRL, and safety databases such as ARGUS. Works closely with Safet...
americans with disabilities actstandard operating proceduresmusic makingmedical reviewadverse eventscase processingaudio masteringSkill required: Pharmacovigilance - Pharmaceutical Drug Safety Surveillance Designation: Management Level - New Associate Job Location: accounts payableaccounts payablereceivableapproval processbudgetingcreditdata entrydrug safetyadverse eventsbusiness processmeddra codingbasicvisitdealsdesign
Job Purpose: The Senior Clinical Data Analyst (SCDA) independently performs/lead and/or coordinate all clinical data validation activities on assigned projects, commensurate with experience and/or pr...
data managementuser acceptance testingclinical data managementclinical data validationstandard operating proceduresdata entryroot causemusic makingdata analysisJob Title: Clinical Coding Specialist Job Location: Anywhere in India ( Full time home based) Job Overview: Perform medical coding ...
problem solvingcrf designcomputer skillsclinical datadata managementpharmaceutical industrymedical codingmedical terminologyprotocol writingclinical data managementstatements of work sow© 2019 Hireejobs All Rights Reserved