Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs.Perform Site visits (i.e. Sit...

Medical Writer / Technical Content Writer - InternshipThis internship is ideal for someone passionate about simplifying medical or technical information into clear, structured documents and engaging content.Good Knowledge of ...

Should have knowledge in Clinical Data ManagemenShould have good knowledge in edit checks crf design SAE Reconcilation crf annotation Good knowledge in Startup conduct phase and close out phaseRequired Candidate profileStrong...

Should have Strong Knowledge in medical review of ICSRs and PharmacovigilanceKnowledge of safety databases, such as Argus, ARISg.Familiarity with medical coding dictionaries (e.g., MedDRA) and adverse event reporting standard...

Perform triage & intake of ICSR received daily in ARGUS databases within the agreed timelinesProcessing literature, spontaneous clinical trial and solicited casesResponsible for coding events, indications and patient hist...

Job descriptionShould have knowledge in clinical research studies Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits)should have knowledge in ICH GCP Guide...