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...
About the Role Dava Oncology is seeking a Clinical Research Associate (CRA) to support patient-focused programs in collaboration with government medical colleges and public hospitals across India. This role is not a site-monitoring CRO role, but a programmatic CRA position focused on structured patient data capture, longitudinal follow-up, treatment compliance, safety monitoring, and outcomes...
Job Title: Applied AI Consultant – Clinical Research (CRO) Engagement Type: Contract / Part-time / Full-time | Remote/Hybrid | Long-term potential Location: Bangalore We are a Clinical Research Organization (CRO) producing multiple clinical study protocols and reports every month. We maintain a strong internal database of historical protocols and reports, and want to build a practical AI...
Role : Clinical Research Associate Location: Bangalore/Mumbai/Ahmedabad/Delhi Work Mode: Hybrid Work Experience: 3+ year relevant experience Job Overview - Perform monitoring and site management work to ensure that sites are conducting the study and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements Essential Functions -...
Job Title: Clinical Research Associate Scientist III Company: Strand Life Sciences Pvt. Ltd. Location: Bengaluru, India Job Type: Full-Time | Hybrid About Strand Life Sciences Strand Life Sciences is a 25-year-old organization with a strong foundation in biomedical research and healthcare innovation. We are committed to improving human health by supporting high-quality clinical research and...
Job Role: - To coordinate and conduct the clinical studies for new product in line with SOPs, GCP and applicable guidelines- Setting up the trial site and Liaising with doctors/consultants or investigators on conducting the trial- Verify that ethics committee operates and complies as per GCP,SOP and applicable regulatory requirements- Ethics Committee coordination and prepare documents for...
We are seeking an experienced and highly driven Senior Clinical Trial Associate (Senior CTA) to join our clinical research team. The Senior CTA will play a critical role in independently supporting and overseeing the planning, execution, and management of clinical trials, ensuring full compliance with regulatory requirements, GCP guidelines, and company protocols.This role requires strong...
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...
Location: Delhi, Mumbai, Chennai/Bangalore, Kolkata, Hyderabad Job Responsibilities: 1.Clinical Training: Provide comprehensive training to surgeons, operating room staff, and other healthcare professionals on the proper use of our surgical robotic systems. Develop and deliver training programs to ensure proficiency and competency in utilizing the technology. 2.Clinical Support: Collaborate...
Job Title: Clinical Trial Coordinator (Fresher) Location: [Site / Hospital / CRO – specify] Experience: Freshers (0–1 year) Candidates with internship or clinical research training are welcome Qualification: BSc / MSc Life Sciences BPharm / MPharm BSc Nursing / GNM Biotechnology / Microbiology / Biochemistry or related life-science background Clinical Research / GCP training...
Tech Observer (www.tech-observer.com) is a global CRO with presence in 20+ countries. PFB JD (But not limited to) Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles. Ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures. Arrange and...
Company:DSS Imagetech is a New Delhi-based company with offices all over India, providing cutting-edge solutions to researchers and clinicians in various fields of Life Sciences and Healthcare. DSS Imagetech is recognised for its expertise in Micro-Imaging, Clinical Diagnostics, Medical Equipment and R&D. We currently maintain our focus on Research Imaging, Clinical Diagnostics, IVF and Food...
Clinical Services Coordinator Type: Full-time | PaidLocation: Pune (Hybrid) | Partially remote About The ADHD Chapter The 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...
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...
Position Summary: The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This...
About Amaha Amaha is a tech-enabled mental health platform supporting people with psychological needs. The firm is run by a team of mental health, technology, and wellness professionals. We are passionate about changing the lives of millions of people who will benefit from psychological support in all aspects of their lives. With our self-care app, we aim to make psychological wellness more...
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...
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 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities. 2 To submit protocol and other required study related documents to the Ethics Committee (as per the...
JOB DETAILS 1 Performing routine data collection from patients, 2 Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement 3 SOPs (standard operating procedures), and are aligned with the Monitoring Plan. 4 Some clinical research associates assist in reviewing study protocols, informed consent forms, and...