Job SummaryWe are currently seeking a full time, remote based Study Start up Submissions Manager to join our Clinical Operations team in…
Job Description SummaryAs a Country Associate, will be responsible for creating forecasting models and delivering impact files (for new product launches, patent…
By continuing to use and navigate this website, you are agreeing to the use of cookies. Accept ClosePress Tab to Move to…
Department: Global Medical Affairs Bangalore (Regions & Operations)The PositionThe position holder will assist closely in providing strategic and medical guidance covering portfolio…
Job Title: Sr Medical Writer /Medical Writer 2 (Clinical Trial Transparency)Job Location: Gurugram, Haryana, IndiaJob Location Type: On siteJob Contract Type: Full…
Job SummaryWe are currently seeking a full time, remote based Senior Study Start up Submissions Coordinator to join our Clinical Operations team…
Job OverviewJoin global organization with 82000+ employees around the world, as a Lead Frontend Developer based in IQVIA Bangalore. You will be…
By continuing to use and navigate this website, you are agreeing to the use of cookies. Accept ClosePress Tab to Move to…
TMF Specialist I India, Chennai Hybrid: Office basedICON plc is a world leading healthcare intelligence and clinical research organization. Were proud to…
Keeping the vehicle hygenic, clean and presentable. Must have a valid driving license. Knowledge of traffic rules and regulations. Proficiency in using…
DescriptionPosition at WebMDAbout the Company:Headquartered in El Segundo, Calif., Internet Brands\xc2\xae is a fully integrated online media and software services organization focused…
Job Overview:Join global organization with 82000+ employees around the world, as an Power BI Consultant based in IQVIA Bangalore/ Gurugram .You will…
Principal Medical Writer The Principal Medical Writer, will research, create, and edit all documents associated with clinical research. The Principal Medical Writer…
YOUR TASKS AND RESPONSIBILITIES: Develop and update process documents, SOPs and trackers for Medical Writing Function Prepare, review and edit clinical trial…
Job Description:Purpose of Pharmacovigilance Associate Role:The purpose of the Pharmacovigilance Associate role is to monitor and manage the safety aspects of clinical…
Job Summary :We are currently seeking a full time, remote based Study Start up Submissions Manager to join our Clinical Operations team…
Responsibilities:Monitor patient safety during clinical trials by reviewing adverse events, SAEs, and providing medical assessments. Ensure timely and accurate reporting of SAEs…
Job Overview Manage a team of Statistical Programming (SP) staff, including hiring, training, and supervising department members. Develop, recommend, and implement standard…
As a CDC II you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Location :…
b\'Medical Writer Immediate Joiner Job descriptionIndustry: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific CommunicationsPosition: InternReports to : Pubrica Business HeadWork…