Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expendable
Job title : Associate Clinical Data coordinator Experience : 1.5 to 3 years Location : Kochi and Bangalore Mode of work : Office based Job Overvie wPerform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to
Project Role: Associate Data Team Lead/Data Team Lead Work Experience: 8+ Years. Work location: Kochi/Kolkata Work Mode: Hybrid/Homebased Must Have Skills: Clinical data management, Rave, SSU experience. Shift Timings: 5:00 am -2:00 pm / 2:00 pm – 11:00 pm The shift
At Clario, part of Thermo Fisher Scientific. Join us in making clinical trials easier, faster, more engaging, and accessible to all. We are transforming the future of clinical trials. Our Specialty Solutions & Clinical Adjudication team supports some of
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Job Description Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals
Job Title: Clinical Research Associate (CRA)/ Senior Clinical Research Coordinator Company: MS Clinical Research Pvt Ltd Experience: Minimum 3 years About Us MS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct
Associate Manager - Clinical Data Management Experience: 8 Years Key Skills: Clinical Data Management (CDM) EDC & Query Management Data Review & Data Cleaning SAE Reconciliation eCOA / ePRO eTMF Database Lock Activities ICH-GCP CRO/Vendor Management Responsibilities: Review and clean clinical trial data. Manage queries
Job Title: Clinical Research Associate (CRA)/ Senior Clinical Research Coordinator Company: MS Clinical Research Pvt Ltd Experience: Minimum 3 years About Us MS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct
Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (i CRO). We are passionately focused on our vision to Connect Imaging to the Cure TM. Everything we do is aligned with this singular purpose.
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri)