{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/thane/"},"x-facet":{"type":"city","slug":"thane","display":"Thane","count":1},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bf9c13e0-018"},"title":"Medical Advisor/Associate Medical Director","description":"<p>IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies.</p>\n<p>You will support compliance with protocol execution from a medical and scientific perspective. You will provide medical expertise during project delivery lifecycles; provide medical support to project teams and investigative sites; clarify protocols and inclusion/exclusion determinations; advise around patient safety issues; perform medical reviews and clarifications of trial-related and post marketing studies Adverse Events; signal detection and aggregated reporting; and conducting project delivery lifecycles (pre-marketing and post-marketing).</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects.</li>\n<li>Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.</li>\n<li>Contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs).</li>\n<li>Provide therapeutic area/indication training for the project clinical team.</li>\n<li>Attends and may present at Investigator Meetings.</li>\n<li>Performs review and clarification of trial-related Adverse Events (AEs).</li>\n<li>May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.</li>\n<li>May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.</li>\n<li>May perform medical review of adverse event coding.</li>\n<li>Performs review of the Clinical Study Report (CSR) and patient narratives.</li>\n<li>Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.</li>\n<li>Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Medical degree with training in Hematology or Oncology from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.</li>\n<li>Specialty Board certification in relevant specialty area preferred.</li>\n<li>Some years of prior relevant experience in general clinical medicine including experience in the requested applicable medical specialty area or equivalent combination of education, training, and experience.</li>\n<li>Current knowledge of medical, scientific and clinical landscape in applicable therapeutic area.</li>\n<li>Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.</li>\n<li>Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).</li>\n<li>Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li>\n<li>May require occasional travel.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Thane-Maharashtra-India/Medical-Advisor-Associate-Medical-Director---Oncology-Hematology_R1576521","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Thane-Maharashtra-India/Medical-Advisor-Associate-Medical-Director---Oncology-Hematology_R1576521","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Hematology","Oncology","English"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Thane, Maharashtra"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Hematology, Oncology, English"}]}