The Quality Assurance & Clinical Validation Lead will be responsible for establishing and maintaining the Quality Management System (QMS) in compliance with ISO 13485, while simultaneously planning and executing clinical and design validation activities to demonstrate that medical devices meet intended use, user needs, and clinical performance requirements. This role acts as a critical bridge...
Role Overview:We are seeking an experienced Dermatologist to help evaluate and enhance large language model (LLM) outputs in the medical domain. You’ll assess AI-generated clinical content for dermatological accuracy, safety, and relevance — contributing to the development of responsible AI in healthcare.No AI experience required.What You'll Do Day-to-Day:- Review AI-generated medical text for...
Clinical Services CoordinatorType: Full-time | PaidLocation: Pune (Hybrid) | Partially remoteAbout The ADHD ChapterThe ADHD Chapter is a specialised mental health initiative focused on evidence-based care for adults with ADHD and training for mental health professionals. Founded by NIMHANS alumni, the organisation integrates Psychiatric & therapeutic services, advanced professional training, and...
Work Hours:U.S. time zones – requires evening/night shifts in India DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India. This is a fully remote position, but working hours will be based on U.S. time zones, meaning evening and night shifts will be...
The Analyst – Clinical Research plays a key role in developing two main artefacts: Human Readable and Data Dictionary using MAT tool and analyze measure specifications to translate data in clinical form. This role works closely with clinical teams, database management personnel, and project managers. Job Responsibilities: Registry Data Management: Create two main artefacts: Humar Readable and...
The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for production of Key Risk Indicators, working collaboratively across departments to produce quality deliverables within agreed...
As a Principal Biostatistician, you are responsible for statistical activities in support of pre-clinical trials, including assay qualification, dose‑response analysis, data visualization, What we’re looking for: - Minimum Education: Ph.D. or MS in Statistics, Biostatistics or related discipline. - Minimum Work Requirements: - At least 6 years of experience as biostatistician in the...
Job Title: Medical Writer – Fixed Term Contract (12 months, Full Time) - Spinal Devices Locations: India Department: Scientific Operations About the Role: We are seeking a Medical Writer to join a dynamic scientific operations team supporting medical device projects. This is a full-time, site-based role on a 12-month fixed-term contract with the potential for extension. The Medical Writer...
Who we are We are a fast-growing Johns Hopkins startup that is revolutionizing digital health. CurieDx is a mobile app that predicts diseases, like strep throat and urinary tract infections, with a smartphone image and AI analysis. Our mission is to help families feel better, faster, with lab tests on the phone. About the role We're seeking an experienced ML Ops Engineer to operationalize...
Job Title: Senior Statistical Programmer Location: IN/EU(Hybrid/Remote) Employment Type: Full-Time Experience Required: 7+ Years Job Summary We are looking for a strong Senior Statistical Programmer. The role requires hands-on expertise in SAS-based analysis and reporting, CDISC-compliant SDTM and ADaM development, and delivery of high-quality Tables, Listings, and Figures (TLFs) in a...
Overview Cactus Life Sciences partners with the global biopharma industry to drive innovation and elevate patient outcomes through agile, science-driven medical communications. As a growing scientific communications agency, we are seeking a driven leader (designation will be Manager, Quality and Training) to take on this pivotal role that spearheads the training and development of budding...
NOTE - - Looking for only 7+yeras of experience. - This Job requires you to work from PAN India Capgemini office. JOB DESCRIPTION The Statistical Programmer II (SP II) - Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR); - Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the...
Location India (Remote / Hybrid) | Supporting Global (US & EU) Clients Company Anervea.AI About Anervea & AlfaKinetic Anervea is an AI-native pharma intelligence company building next-generation platforms for Competitive Intelligence, Commercial Analytics, and Real-World Evidence–driven decision-making. AlfaKinetic is Anervea’s flagship Competitive Intelligence platform used by global...
Location: Pune (with travel to clinical trial sites across India) Experience: 2–3 years Salary: ₹5–6 Lakhs per annum About the Role We are seeking a Medical Device Test Engineer with hands-on experience in testing medical devices in clinical and laboratory environments. This role involves extensive travel and long-term stays at test sites to ensure rigorous validation and compliance of our...
TransPerfect is a world leader in language and technology solutions, trusted globally for more than 25 years. We are expanding our network of freelance linguists and agencies, and we invite agencies with teams experienced in Indic languages to collaborate with us on English (US) into Indic languages Clinical Research Protocol (CRP) translation and proofreading projects. We are specifically...
Hiring for Senior Manager / Ass Director - Marketing Location: Bangalore/Remote Knowledge and Application - Expertise in external client facing marketing and communications. - Expertise in supporting business development proposals. - Understanding of clinical research organization operations. Key Responsibilities and Authorities Candidate - Marketing will lead external communications and...
Role Summary We are seeking a highly experienced Senior / Lead Statistical Programmer for a part-time engagement to support clinical trial programming activities within a CRO environment. This role is ideal for seasoned professionals who can provide deep technical expertise, quality oversight, and delivery leadership on a flexible schedule. The role focuses on advanced SAS programming, CDISC...
The Clinical Study Builder will work closely with data management and statistical staff to design and develop electronic case report forms (eCRFs), visit schedules and associated data quality checks for medical research studies. This position is required to work in a dynamic and collaborative environment. In addition, solution creation includes implementation , testing, and system integrations....
The Advisor Clinical Research plays a key role in developing two main artefacts Human Readable and Data Dictionary using MAT tool and analyze measure specifications to translate data in clinical form. This role works closely with clinical teams, database management personnel, and project managers. Job Responsibilities: Registry Data Management: Create two main artefacts: Humar Readable and...
About Turing: Turing is one of the world’s fastest-growing AI companies, accelerating the advancement and deployment of powerful AI systems. Turing helps customers in two ways: Working with the world’s leading AI labs to advance frontier model capabilities in thinking, reasoning, coding, agentic behavior, multimodality, multilinguality, STEM, and frontier knowledge; and leveraging that work to...