Clinical Content Developer Medical

Subject Matter Expert (SME) — Medical / Nursing Education (VR Training Content)Engagement Type: Full-time / Part-time Consultant (3-month pilot)Location: Flexible / Remote + occasional on-site sessions at XploR Medica, BengaluruDuration: 12 weeks (extendable based on pilot success)Reporting to: Project Lead – Immersive Training (XploR Medica)Who you...

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdExperience: Minimum 3 yearsAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the...

At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to...

Job Title: Senior Clinical Research Associate (Sr. CRA)Company: MS Clinical Research Pvt LtdExperience: Minimum 5 yearsAbout UsMS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct high-quality clinical trials that adhere to global standards of...

Primary Responsibilities:Test case creation and executionTesting new features being developed to make sure the product is functionally & clinically viableTesting clinical rules/patterns being developed to ensure the rule correctly captures the essence of the sourced clinical/medical guidelinesEnsure the product is compliant to the US Healthcare systemWork...

Senior Medical Writer IQVIA is looking for candidates who have expertise in regulatory writing to join our Real World Evidence team. The Ideal candidate will have 5-12 years of experience working as Regulatory Medical Writer, adept in developing and authoring clinical study protocols, informed consent documents, clinical study reports. ...

Senior Medical Safety Advisor Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product's safety profile as...

Associate Medical Safety Director Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety...

Job OverviewProvide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential Functions• Perform...

Job OverviewProvide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential FunctionsPerform...