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...
**Career CategoryInformation Systems**Job Description**Join Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four...
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...
Ready to shape the future of work? At Genpact, we don’t just adapt to change—we drive it. AI and digital innovation are redefining industries, and we’re leading the charge. Genpact’s AI Gigafactory, our industry-first accelerator, is an example of how we’re scaling advanced technology solutions to help global enterprises work smarter, grow faster, and transform at scale. From large-scale models...
JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3. Review informed consent document /...
ARI has initiated this stand-alone F2F internship program at many of its locations to provide hands-on training after a basic theoretical knowledge in clinical Research. It gives the opportunity to the candidate to get a peek into live trial conduct and enables them to understand the practical domain in a better way. In an internship, it is the hands-on practice approach under the shadow of an...
Position Overview: The Associate Director of CSC Business Capabilities plays a pivotal role in overseeing and optimizing the functions within the Clinical Supply Chain (CSC). The Associate Director leads a team that provides Clinical Supply Chain (CSC) representation for Interactive Response Technology (IRT), Clinical Supply Chain Logistics (CSCL) and Business Operational activities related to...
Hey there! Are you a compassionate and skilled Clinical Psychologist looking for an exciting opportunity to make a real difference in people's lives? Look no further! At DISHA LAW FIRM, we're on the hunt for a talented individual like you to join our dynamic team. Our firm is dedicated to providing top-notch legal services, but we also recognize the critical role mental health plays in the...
Locations: Hyderabad Department: Clinical Development Centre-India Novo Nordisk India Pvt. Ltd. Are you a skilled medical professional with a passion for Clinical development strategy and a drive to make a real impact? Join Novo Nordisk as a Clinical Medical Manager and be part of a fast-growing, dynamic team where your expertise will shape strategy and execution of Novo Nordisk pipeline in...
Clinical Specialist / Stroke Rater – Punjabi Speaking Location: Remote Hours: Estimated 2–12 hours per month, flexible Role Overview The Clinical Specialist supports stroke clinical trials byadministering standardized assessments and ensuring data quality and consistency. This includes rating patients using validated stroke scales and reviewing assessments performed by other raters to maintain...
Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic...
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of...
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...
Job Title/Role: Sr. Support Manager, Interactive Response Technology Department Name/Functional Area: Global Clinical Supply Chain > Clinical Supply Chain Technologies > IRT Location: Office based. Position Summary - This position supports multiple IRT studies (system development, study management, change management, audits and data provisioning). Supports UAT Services organization as...
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...
JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee regarding rights, safety and...
Description The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trialsSuccessfully leads, plans, and...
JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee regarding rights, safety and...
JOB DETAILS 1 Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. 2 Provide expert medical/scientific advice for assigned products and related therapeutic areas, including...
JOB DETAILS 1. Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions 2. Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol...