25 Clinical Studies Jobs

As the Director Medical AI & Innovation at Novartis, you will be a key member of the Global Medical Affairs team, leading the medical strategy for the therapeutic area. Your role will involve developing and owning Integrated Evidence Plans (IEPs), providing input into development processes, and ensuring that both US and international medical perspectives are reflected. You will be responsible for implementing medical strategies for early programs globally, focusing on innovative evidence solutions such as interventional studies, Non-Interventional Studies (NIS), Real-World Evidence (RWE) studies, and implementation science projects. Your extensive experience in drug development will enable y...

Position Code : IIPHH-RF-06 Position Title : Research Fellow PANPREP- Dr. Cyrus Poonawalla Centre for Infectious Diseases and Pandemic Preparedness No. of Positions : 01 Location : IIPH Hyderabad Duration of Position requirement : Initially for 1 year, extendable based on the position Brief On The Organization The Indian Institute of Public Health Hyderabad (IIPH, H) commenced with a mission to deliver public health education, pursue research and advocacy and support policy development. It lays strong emphasis on pursuing public health policy, practice, training and research, positioning its programmes according to the public health priorities of the state and the nation. The institute has b...

Role Overview: As an Associate Scientific Director at Red Nucleus, you will be a key member of the Medical Communications team. Your role will involve leading scientific accounts, providing high-quality editorial review, and acting as a scientific and therapeutic expert for assigned project teams. You will set standards for content development, mentor medical writing staff, and support business development efforts. Key Responsibilities: - Set standards for the assigned team to drive continuous improvement in quality and client interactions - Evaluate internal processes related to content development and suggest improvements - Ensure high-quality outputs from the scientific team - Identify tr...

Role Overview: As a Scientific Advisor (MSL) for Rare Blood Disorders, your role involves combining technical and scientific expertise to plan and communicate effectively with internal and external partners. You are responsible for engaging with Key Opinion Leaders and healthcare professionals to discuss recent scientific evidence, clinical studies, and disease management within the therapeutic area of Rare Blood Disorders, with a focus on Hemophilia. Key Responsibilities: - Plan, organize, and execute field activities to disseminate medical knowledge and update healthcare professionals on the therapeutic area of Rare Blood Disorders - Provide information on relevant clinical studies and tre...

As a Manager/Sr Manager in the Medical Affairs team for Emerging Markets, your role will involve supporting the initiation, oversight, and follow up of clinical studies and medical projects within the therapeutic area under your responsibility. You will be responsible for utilizing tools, templates, and processes to create and deliver presentations for training, CMEs, and conferences while ensuring compliance with UpToDate guidelines and recent updates. Key responsibilities for this role include: - Identifying key opinion leaders (KOLs), expert speakers, and academicians in the industry to deliver defined curriculum with technical and clinical insights - Developing training and educational m...

As an R&D Biomedical Engineer, you will specialize in the research and development of biomedical technologies. Your role will involve designing, developing, and optimizing medical devices and systems to enhance healthcare delivery. Your expertise will contribute to innovation in medical technologies, advancing patient care and ensuring compliance with regulatory standards. By leading the development of cutting-edge solutions, you will play a key role in improving the safety, functionality, and reliability of critical healthcare equipment. Key Responsibilities: - Lead and coordinate research for the development of new medical devices, ensuring compliance with regulatory standards (CDSCO, FDA,...

Job Description: As a Clinical Psychiatrist at Tulasi Healthcare, your role will involve treatment planning, psychiatric care, specializing in psychiatry, medicine, and adolescent psychiatry. You will be responsible for providing direct patient care and collaborating with the multidisciplinary team to ensure comprehensive treatment plans and outcomes. Key Responsibilities: - Develop treatment plans for patients - Provide psychiatric care with a focus on psychiatry, medicine, and adolescent psychiatry - Collaborate with multidisciplinary teams for holistic patient care Qualifications: - Specialization in Psychiatry and Medicine - Expertise in Adolescent Psychiatry - Ability to collaborate eff...

As a Technical Configuration Specialist at our company, your responsibilities will include: - Performing the technical configuration of the CluePoint Central Monitoring Platform solution for clinical studies based on requirements. - Leading technical study level set-up and supporting ongoing refreshes based on defined frequency. - Creating templates and leading Prep Meetings with CM to review analysis set-up and dashboards in preparation for study team meetings. - Creating various dashboards such as KRI, DQA, QTL, and SPOT. - Managing Study Configuration and supporting CM in defining study requirements. - Ensuring pre-processing activities are complete, such as data availability (pre-defined...

As a member of the team, your role will involve designing and analyzing clinical and observational studies related to cost-effectiveness and health outcomes. You will also be responsible for supporting the development and validation of economic models, such as Markov and decision trees. Conducting sensitivity analyses and interpreting statistical outputs for economic evaluations will be part of your daily tasks. Additionally, you will collaborate with health economists, epidemiologists, and clinical researchers to ensure the success of various projects. Qualifications required: - Previous experience in designing and analyzing clinical studies - Proficiency in conducting sensitivity analyses ...

Manager/Sr Manager- Medical Affairs (Emerging Markets) Support the initiation, oversight and follow up of clinical studies and medical projects initiated within the therapeutic area for which the carries responsibility Utilizes the tools, templates and processes that create and deliver the PPTs for training, CMEs and various conferences with UpToDate guidelines and recent updates. Identify key opinion leaders (KOLs) in the industry, expert speakers, and well-known academicians who can deliver the defined curriculum provide technical and clinical insight with real-world applications Develop training and educational materials and programs. Responsible for management of all educational content ...

As the Head of Clinical Research at PredOmix, you will lead the clinical research group to advance metabolomics-based technology for early and accurate cancer detection. Your responsibilities will include: - Proficiency in laboratory protocols, focusing on serum metabolite extraction and daily laboratory procedures following GLP guidelines. - Development and execution of clinical studies in alignment with the company's strategic goals. - Ensuring timely and efficient completion of clinical projects with independence and creativity. - Contribution to the regulatory process for the company's products. - Establishment and management of collaborations with clinicians and hospital partners. - Col...

As a candidate for the role of supporting the Clinical Developments (CD) portfolio at Novartis, you will work closely with the Head of Business Operations. Your role will involve the following key responsibilities: - Running portfolio analysis of clinical studies and projects for all Development Units (DUs) by collecting information from various sources like Andromeda, Horizon, BoW. - Compiling insights and providing analysis of the expected evolution of the portfolio, simulating various scenarios and their impact on resourcing, capability, and overall plans. - Establishing visualization and ongoing reporting of key portfolio insights. - Supporting the creation, implementation, and refinemen...

As a Statistical Programmer I, you will be responsible for creating, testing, and maintaining programs for clinical studies using SAS. Your key responsibilities will include: - Using SAS to generate summary tables, data listings, graphs and derived datasets as per statistical analysis plan and programming specifications. - Ensuring that outputs meet quality standards and project requirements. - Performing validation programming and collaborating with team members to resolve discrepancies. - Keeping project team members informed of programming progress and issues. - Following SOPs and relevant regulatory guidelines. - Maintaining well-organized project documentation and verification/quality c...

As a Statistical Programmer, your role will involve providing statistical input to the design, analysis, reporting, and interpretation of clinical studies, as well as contributing to publications. You will utilize SAS or other software to develop custom programming code for generating tables, data listings, graphs, and derived datasets as specified in the protocol or statistical analysis plan. Ensuring that all outputs meet quality standards and project requirements is crucial in this role. Key Responsibilities: - Perform validation programming and collaborate with other Programmers, Biostatisticians, and project team members to resolve any discrepancies or findings. - Keep the project team ...

a. Should be well versed with IVIVC concepts b. Should have excellent knowledge on product development and clinical studies. c. Should have hands on experience on operating various simulation tools necessary for IVIVC. d. Excellent communication skills are must. Excellent knowledge on product development and clinical studies

Role Overview: The Director, Clinical Operational Data Governance at GSK plays a crucial role in driving the governance and management of clinical operational data to support groundbreaking research and development efforts aimed at delivering transformative medicines. Your primary responsibility will be to ensure the availability of high-quality operational data from clinical studies, supporting informed decision-making for current and future clinical pipeline activities. As a key player in shaping the future of healthcare, you will play a pivotal role in ensuring the integrity and accessibility of operational data that drives our clinical studies, ultimately enabling us to bring innovative ...

The role of Veeva CTMS Configuration Specialist involves a range of responsibilities related to Veeva Vault CTMS & TMF. You will be responsible for initiating and overseeing all changes and implementations within the Veeva Vault CTMS & TMF systems. It will be essential for you to thoroughly understand business requirements and devise appropriate technical solutions to address them. Your role will also entail leading various technical design and implementation meetings, ensuring that all work done by other configurators is reviewed for accuracy and efficacy. Additionally, you will be accountable for managing and executing deployments, which involves tasks such as preparing deployment checklis...

As the Medical Science Liaison, your primary responsibility is to develop and maintain in-depth knowledge of assigned products and relevant therapeutic areas. This involves actively participating in internal meetings, training sessions, congresses, seminars, and staying updated with national and international literature through self-study. You will be expected to provide expert medical and scientific advice for assigned products, respond to requests for scientific information, and contribute to the development of core dossiers. Building and nurturing professional relationships with key opinion leaders and academic centers will be crucial, including organizing and participating in scientific ...

At Medtronic, you can embark on a lifelong career dedicated to exploration and innovation, all while advocating for healthcare access and equity for all. Your role will be purpose-driven, aimed at breaking down barriers to innovation in a more interconnected and compassionate world. As a Clinical Research Specialist at Medtronic, based in India, your responsibilities will include overseeing, designing, planning, and developing clinical evaluation research studies. You will be involved in preparing and authoring protocols and patient record forms, as well as conducting clinical studies of products that address medical needs or have commercial potential. You will interpret the results of clini...

As a Clinical Education Specialist, your primary responsibility will be to support the initiation, oversight, and follow-up of clinical studies and medical projects within the therapeutic areas of Virology, Hormonal, Blood related, and Antibiotics. You will utilize various tools, templates, and processes to create and deliver presentations for training, Continuing Medical Education (CME) programs, and conferences, ensuring alignment with Up To Date guidelines and recent updates. Your role will involve identifying key opinion leaders (KOLs), expert speakers, and academicians in the industry who can provide technical and clinical insights with real-world applications. Additionally, you will be...

The Clinical Database Programmer (CDP) within the Global Clinical Data Management (GCDM) department is responsible for managing Clinical Data Programming activities. Your role involves ensuring the timely creation, validation, testing, implementation, and maintenance of databases required for all assigned projects. You will analyze study protocols and project requirements, identify data quality rules, and design data entry interfaces in compliance with study protocols, Data Management Plans (DMP), Standard Operating Procedures (SOP), and relevant regulatory requirements and standards. You will be responsible for deploying complete, accurate, and efficient clinical study databases to support ...

Job Purpose Responsible for the design and oversight of safety pharmacology, exploration, and GLP-compliant toxicology studies. Manage multiple projects efficiently across various stages of discovery, preclinical, and clinical development. Contribute to the preparation and review of regulatory submissions and engage with regulatory authorities and cross-functional asset teams This position is located in Hyderabad, Telangana, India. Duties And Responsibilities : Preclinical Pharmacology Design, supervise, and interpret in vivo efficacy studies using a range of disease models. Provide scientific and technical oversight for preclinical pharmacology programs. Prepare study proposals, budgets, an...

Project entitled :- Investigating the clinical relevance of environmental chemicals and exosomal miRNA biomarkers in the pathophysiology of Polycystic Ovary Syndrome funded by Indian Council of Medical Research. Name of the Post :- Project Research Scientist-I (Medical) No. of vacancy :- One Consolidated Salary :- Rs.87,100/- (Rs.67,000/- plus 30% HRA) Essential Qualification Desirable / Job Responsibilities :- MBBS / BVSc / BDS or equivalent. Desirable Qualification / Job Responsibilities :- Research experience in clinical studies. Experience in writing reports/manuscripts He/she will be looking after overall implementation of the project. He/she will be engaged in screening of the particip...

Outpace Consulting Services is seeking a Medical Writer specializing in Life Sciences and Clinical Studies for a leading ITES company. This role is responsible for developing clear, accurate, and well-structured medical and scientific documents for various audiences, including regulatory authorities. You'll translate complex clinical and scientific data into understandable content for regulatory submissions, clinical trial documentation, and other critical materials. The ideal candidate will have strong writing skills, a solid understanding of medical terminology and research practices, and experience with regulatory submission formats. Key Responsibilities: Clinical Document Preparation: Pr...

a. Should be well versed with IVIVC concepts b. Should have excellent knowledge on product development and clinical studies. c. Should have hands on experience on operating various simulation tools necessary for IVIVC. d. Excellent communication skills are must. Excellent knowledge on product development and clinical studies