Medical Affairs
6 days ago
Medical Affairs Co-Founder – Evidence AI Platform (OneRx.ai)Location: Gurgaon, India | Full -Time | Evidence Intelligence & Ai HealthTechAbout OneRx.aiOneRx.ai is India’s first Evidence Intelligence Platform for Doctors , being built on trusted sources like ICMR, NEJM,, and PubMed among others— powered by a medical-grade AI engine.We are a self-funded startup building an AI powered future of clinical decision-making , where every doctor can access clear, cited, and contextual evidence in seconds.We are looking for a medical affairs lead to power medical intelligence in the team. This person will be a part of the core founding team and make a difference to the product and the marketRole OverviewWe are looking for a Medical Affairs Pharmacologist who wants to move beyond traditional roles and help build the next generation of AI-powered medical evidence product .This is a hybrid position combining clinical knowledge, product innovation, and hospital collaboration — ideal for someone excited by science, technology and entrepreneurship .Key ResponsibilitiesAI Product Development:Co-create therapy wise evidence modules with the product and tech teams, starting with onco.Evidence Curation:Identify, summarize, and validate key trials, drug studies, and treatment guidelines for integration into OneRx’s evidence engine.Hospital & Doctor Partnerships:Build collaborations with doctors, hospitals, oncology departments, for pilots and validation.Doctor Engagement & Training:Introduce the product to oncologists, and other therapy area doctors; conduct demos, training sessions, and workshops to ensure adoption.Product Testing with Clinicians:Lead user trials, gather real-world feedback, and translate findings into product improvements.Cross-Functional Collaboration:Work closely with AI, engineering, and UX teams to align clinical logic with product design.Thought Leadership:Represent OneRx at medical conferences, digital health forums, and academic partnerships; publish and speak on evidence-based AI in oncology and pharmacology.Who You AreEducation: MBBS + MD (Pharmacology, or related specialty)Location: Gurgaon (preferred)Skills:Building hospital and doctor partnershipsConducting demos and training programs for doctorsTranslating clinical insights into product logicCollaborating across medical, product, and engineering teamsExcellent scientific writing and communicationBonus: Experience in medical affairs, AI tools, or evidence synthesis platformsWhy Join UsShape the future of evidence-based healthcare in IndiaCollaborate with AI engineers, data scientists, and medical expertsBuild and test products used by doctors nationwideCompetitive compensation, ESOP potential, and high-growth trajectoryWhat you should know about usWe are a young company, 12 people with inhouse AI tech teamWe are self fundedWe believe in making a difference through the work we doCompensationWill be fixed monthly and founder equityApply Now “Application – Co-Founder Medical Affairs AI & Product”
-
Medical Affairs
5 days ago
Faridabad, India OneOrg.AI | Business AI Full timeMedical Affairs Co-Founder – Evidence AI Platform (OneRx.ai)Location: Gurgaon, India | Full -Time | Evidence Intelligence & Ai HealthTechAbout OneRx.aiOneRx.ai is India’s first Evidence Intelligence Platform for Doctors , being built on trusted sources like ICMR, NEJM,, and PubMed among others— powered by a medical-grade AI engine.We are a...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: - Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.). - Ensure compliance with ISO 13485, EU...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.). Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:- Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).- Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India Whatjobs IN C2 Full timeRole Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: Prepare and compile regulatory submissions (e.G., Device Master File, Technical File, 510(k), CE marking, etc.). Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.). Ensure compliance with ISO 13485, EU MDR...
-
Regulatory Affairs Specialist
2 weeks ago
Faridabad, India vueverse. Full timeRole Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:- Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).- Ensure compliance with ISO 13485, EU MDR...
