8317 Clinical Research Jobs - Page 14

To support the development, dissemination, and maintenance of Value & Access (Health Economics & Outcomes Research [HEOR]) deliverables for selected key strategic asset/s for a specific disease/condition. Deliverables Cost effectiveness models, budget impact models and their updates, and other activities as directed by clients (across Novartis - Pharma / Oncology / Sandoz) About the Role Location - Hyderabad #LI Hybrid About the Role To support the development, dissemination, and maintenance of Value & Access (Health Economics & Outcomes Research [HEOR]) deliverables for selected key strategic asset/s for a specific disease/condition. Deliverables Cost effectiveness models, budget impact mod...

Creation of high-quality highly-complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery. About the Role Associate Director Global Publications & Foundational Content Location - Hyderabad #LI Hybrid About the Role Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across th...

This position typically refers to any employee within the EPD Medical organization with medical /scientific qualifications and training who provides scientific/ medical support to EPD in a non-sales capacity, where the provision of such scientific/ medical support includes significant contact with Abbott customers in the field. This definition is not intended to apply to those employees whose primary job function relates to the monitoring or management of clinical studies. Reporting into the Senior Manager RMA / Head RMA this position participates in the initiation, oversight and follow-up of assigned clinical studies and medical projects initiated within the EPD Medical Organization, ensuri...

Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review. Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. Provide training and guidance to the case processing team on medical a...

Examine and diagnose patient conditions with the help of tests. Based on their findings, they prescribe treatment and medications to attempt to heal any illnesses. Providing treatment and follow - up on their patients progress. Making notes and preparing paperwork, both as a legal record of treatment and for the benefit of other healthcare professionals.

Meet the Team The Regulatory Affairs & Compliance team within Ciscos Legal department is comprised of lawyers, program managers, operational specialists, engineers, and subject matter experts focused on topics including compliance and ethics (anti-bribery and anti-corruption), global trade, cybersecurity, telecom, environmental sustainability, and various other regulatory practice areas and programs. We partner with colleagues in Legal and functional teams across the company to drive compliance and impact. The team is seeking a highly skilled and experienced Principal Corporate Counsel to advise on telecommunications regulations, lawful intercept laws and other market access regulatory issue...

Role Description: The International Regulatory Lead (IRL) Sr Associate will provide coordination and execution of regulatory deliverables for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams to optimize product development and regulatory approvals in International countries develop international regulatory strategy and provide regulatory support for in-country product registrations and life cycle management. Roles & Responsibilities: With support, advises Global teams on regulatory implications and requirements relevant to the global clinical development, Marketing Applications plans and objectives. Lia...

Key Responsibilities Manage the entire slot game production lifecycle from concept to launch and post-launch support. Coordinate with designers, developers, artists, animators, sound designers, and QA teams. Develop and maintain project schedules, budgets, and resource plans. Communicate project status, risks, and milestones to stakeholders and senior management. Ensure all slot games comply with industry standards and regulatory requirements. Drive team collaboration and maintain a productive work environment. Identify and implement process improvements to enhance efficiency and quality. Support marketing and business development teams with launch strategies and promotional activities. Mand...

Vacancy in Pharma and Chemical Industry at Chennai Designation - Quality Chemist / Production / ETP / Lab / Microbiologist / Biotechnologist Exp - 0 to 5 yrs

As a Clinical Researcher at Clinikally, you will be spearheading key areas of clinical research focusing on the science behind consumer health solutions. Your role will involve partnering with clinical collaborators globally to conduct efficacy studies on OTC and Rx-grade products in dermatology and nutrition. Some of the solutions you will be researching include the Hyaluronic acid serum, Vitamin C Serum, and a unique DMS technology-based moisturizing lotion. Key Responsibilities: - Undertake robust, verifiable, and in-depth clinical research on Clinikally's consumer health solutions - Conduct efficacy studies on a variety of products in dermatology and nutrition - Collaborate with clinical...

You will be responsible for: - Designing and analyzing clinical and observational studies related to cost-effectiveness and health outcomes - Supporting development and validation of economic models (e.g., Markov, decision trees) - Conducting sensitivity analyses and interpreting statistical outputs for economic evaluations - Collaborating with health economists, epidemiologists, and clinical researchers Qualifications required: - Relevant educational background in health economics, epidemiology, or a related field - Experience in conducting economic evaluations and analyzing health outcomes data The company offers health insurance and Provident Fund benefits for this full-time position with...

As a Medical Assistant in this role, you will be responsible for supporting consultants in both Outpatient (OP) and Inpatient (IP) patient care. Your duties will include assisting consultants in delivering our specialized clinical services. Additionally, if you have an interest, you will have the opportunity to contribute to clinical research work. **Qualifications Required:** - MBBS degree **Working Hours:** - 9:30am to 6:30pm, Monday to Saturday The compensation for this position ranges from 45k to 55k per month, depending on your experience and the quality of work you deliver. As a Medical Assistant in this role, you will be responsible for supporting consultants in both Outpatient (OP) a...

We are looking for a highly skilled and experienced Sales Operations Coordinator to join our team. The ideal candidate will have a strong background in sales operations and coordination, with excellent communication and organizational skills. Roles and Responsibility Coordinate and manage sales operations activities, including lead generation, customer engagement, and sales pipeline management. Develop and implement effective sales strategies to achieve business objectives. Collaborate with cross-functional teams to ensure seamless sales operations processes. Analyze sales data and performance metrics to identify areas for improvement. Provide exceptional customer service and support to clie...

Summary of Responsibilities: Management of projects under direction of a Project Manager/Director as assigned. Ensure site monitoring responsibility for clinical studies is conducted according to Fortrea Standard Operating Procedures (SOP), ICH Guidelines and GCP. Work closely with project teams in implementation of best trip report review practices and applicable project plans as assigned (implementation of Initiatives either independently or with team). Proactively identified opportunities for process improvements and work collaboratively with project team in case further action required. Complete required training within timelines and ensure training resources are up to date with changes ...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digita...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS To determine whether all trial related activities were conducted, data recorded, analyzed and reported accurately & in compliance to all applicable Regulatory requirements, Organizational requirements (Policy, Procedures and processes) a...

Cotiviti Hiring Subject Matter Expert (SME) Program: Coding Validation Educational Qualification : MBBS / BAMS / BHMS / BPT Certification : CPC certification is mandatory (CPC Pursuing Candidates can also apply. Relevant Experience : E&M or IPDRG Speciality candidates are preferrable Experience : Min 3+ Years Position Summary SME will be responsible for analyzing and interpreting the correct codes for the descriptions available on various medical procedures and diagnosis and other related medical coding as per the medical policy requirements, ensuring work delivery as per set expectations while maintaining the required quality standards. Also, the SME would be responsible for extending proce...

Expertise in Geriatric Medicine, including diagnosis, treatment, and management of age-related health conditions. Strong clinical skills in chronic disease management, preventive care, and rehabilitation for seniors. Ability to collaborate with interdisciplinary teams, including nurses, physiotherapists, and caregivers. Experience in patient communication, medication management, and clinical supervision.

We are looking for an a nalyst to join our Immune & Inflammation team in Noida , India. The role comprises three broad functions: 1) market research and insights generation; 2) project management and execution; and 3) client service. The a nalyst will translate therapeutic expertise and market research data into targeted insights for key decision-makers within the biopharmaceutical industry. Areas of coverage will span the teams diverse research portfolio in autoimmune disorders. The team consists of around 12 colleagues based in India, Spain, and the United State s and is reporting to the respective team managers. We have a great skill set in the market research domain related to healthcare...

Align Prescription. Do IP Billing / OP Billing. Check In house ware. Arrange emergency local purchase. Dispersal of medicines for OP and IP. Remove expiring items. Replacing of expiring medicines from different departments. Stock out monitoring. Discharge medicines handling Any other principal duties and key tasks assigned by the management from time to time.

Coordinate the scheduling, logistics, and execution of central review activities, including imaging assessments, laboratory analyses, and other centralized evaluations. Collaborate closely with study teams, clinical sites, and external vendors to ensure timely and accurate collection, transfer, and interpretation of clinical trial data. Monitor the progress and quality of central review processes, proactively identifying and addressing issues or deviations to ensure adherence to protocol requirements and regulatory standards. Maintain comprehensive documentation and records of central review activities, ensuring compliance with data management procedures and regulatory requirements. Provide ...

We are currently seeking a Central Review Lead to join our diverse and dynamic team. As a Central Review Lead at ICON, you will play a pivotal role in overseeing and coordinating centralized review activities for clinical trials, contributing to the advancement of inNvative treatments and therapies. What you will be doing Lead and oversee the planning, execution, and monitoring of centralized review activities, including imaging assessments, laboratory analyses, and other centralized evaluations. Collaborate closely with study teams, clinical sites, and external vendors to ensure the timely and accurate collection, transfer, and interpretation of clinical trial data. Develop and implement st...

We are seeking qualified B.Pharm / M.Pharm professionals to support pharmaceutical operations including production, quality assurance, Please call- 9845514305 / 8050011328

Manages a team of professional-level employees. Develops and communicates plans and priorities to meet team performance and results requirements. Essential Functions Manages a team of professional-level employees. Develops and communicates plans and priorities to meet team performance and results requirements. Establishes team processes, goals, and procedures and tracks performance. Informs and influences decision-making at the management level. Provides coaching and guidance on job performance and career development to direct reports. Qualifications Bachelors Degree Computer Engineering, Computer Science or related field Req 5-7 years+ experience in software development 5+ years of experien...

Managing assigned monitoring responsibilities (simple protocols/ non-protocol tasks) competently, in a timely manner and with quality. Essential Functions Under minimal supervision perform centralized monitoring activities for the assigned projects which includes but is not limited to On time completion of assigned role specific trainings (self-learning courses, instructor led training, acknowledgement of e-SOP/WI etc) and related assessment Loading and updating the active databases with details of participating sites Provisioning of access for Infosario Portal Ensuring on-time completion of documentation(s) that form a part of the regulatory dossier for kit shipment [Kit Contents Chart(KCC)...