Clinical Research Scientist

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...

Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. Essential Functions - Provide clinical research support...

**Educational qualification** **Years of experience** **Job Scope/ Purpose** Research Scientist / RS Educational qualification Ph.D in Organic Chemistry or related field 1-5 years - Excellent knowledge of basic and advance organic chemistry. - Very good knowledge of functional group conversion and multiple step synthesis. - Knowledge of retrosynthetic...

TCS is Hiring -Clinical Safety Scientistlocation - Mumbai, Noida, BengaluruExperience Range - 5 to 10Preferred Educational Qualification for the role - Any life science GraduateJob DescriptionLiterature ReviewLiterature review to assess ICSR, new safety signal, for inclusion in Aggregate report, for inclusion in DSR (Drug Safety reports).Provide MAH comments...

Job Title: Clinical Research Associate (CRA) - Ayurveda Job Summary: Key Responsibilities: 1. Clinical Trial Management: Manage clinical trials from initiation to close-out, ensuring compliance with GCP, regulatory requirements, and company SOPs. 2. Site Management: Coordinate with research sites, investigators, and site staff to ensure timely trial...

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...

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...

Our Company Changing the world through digital experiences is what Adobe’s all about. We give everyone—from emerging artists to global brands—everything they need to design and deliver exceptional digital experiences! We’re passionate about empowering people to create beautiful and powerful images, videos, and apps, and transform how companies...

Principal Data Scientist/Senior Data Scientist/Data Scientist - NLP/Machine LearningJob Role Responsibility:We are looking for passionate, Strong experience with an entrepreneur mindset to join us as Hardcore Full Stack Data Scientist end-to-end single-handed multi-hat role who is already working in applied AI in ML, deep Learning, ANN, and CNN platform...

Job Description New Opportunity for Data Scientist || Immediate to 30days Joiners Job Description Data Scientist (NLP/ML Research) Position: Data Scientist Location: [Hybrid Noida Office] Experience: 2+ years Team: AI/ML Advanced Research and Product Innovation Reports To: Director Data Science About the Role We're seeking a seasoned Data Scientist to lead...