11 Clinical Studies Jobs

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