3474 Clinical Trials Jobs - Page 39

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Experience working in Client On-boarding, Account Maintenance, Customer Identification Program (CIP) and Know Your Customer (KYC) processes.Conducting PEPs (Politically Exposed Persons) screening and adverse media checksProven analytical skills, problem solving ability, and a control mentality paired with meticulous attention to detail.Aptitude for building relationships and ability to communicate complex issues to a wide array of internal clients with differing levels of product experience.Sel...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

Responsibilities: Assist in designing business collaterals, including presentations, reports, and promotional materials. Create visual content for events, such as flyers, posters, banners, and social media posts. Develop business videos, mailers, and digital assets to support marketing campaigns. Support the execution of design projects from conceptualization to completion. Collaborate with other teams to understand project requirements and provide design solutions. Maintain high-quality standards and consistency in design across all materials. Contribute to the overall creative process and offer suggestions to improve design and layout. What are we looking for Bachelors or Masters degree in...

Role & responsibilities To support the QA department (Maintenance of QMS documents) & CSV Computer System Validation & Training Records. Manage the auditing process and keep detailed records. To collaborate with the QA team to ensure that the different departments meet the quality standards and collaborate in the audits contracted by suppliers and internal auditors. All this under the established standards in terms of SOPs, Good Clinical Practice, and the needs of the client. Provide advice, interpretation, help and training to other departments, in GCP, SOPs, regulatory issues and internal company policies related to Quality Assurance. Manage in the definition of internal tools and remote a...

You will use and develop your clinical expertise (including independent prescribing where applicable), working with a cohort of patients as part of a multidisciplinary practice team Part of the role will also include ensuring quality and cost effective prescribing within GP practices to meet NHS Ayrshire & Arrans efficiency savings Knowledge, Training And/or Experience Required To Do The Job Master of Pharmacy Degree or equivalent, Member of the General Pharmaceutical Council of Great Britain (including evidence of continuing professional development), Vocational Training (Level 2) or training experience to an equivalent level, Relevant experience as a pharmacist and dealing with prescribers...

Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries May also provide statistical support to research or other R&...

Step into a role where innovation meets impact As a Digital Endpoint Expert, youll be a key member of the Digital Endpoint Capability Centre, driving the coordination, implementation, and deployment of digital endpoints and digital health technologies across clinical trials Youll bridge digital health expertise and clinical trial excellence, working closely with trial teams and cross-functional stakeholders to ensure seamless delivery Your leadership will shape the integration of novel measures across the development organization, while your expertise will help define implementation strategies tailored to each indication and trial design If you're passionate about digital health and ready to...

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics and APIs, comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research and Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another a...

Position: Biostatistician Location: Nashik Experience: Minimum 2 Years Notice Period: 15 - 30 Days Qualification: Bachelors or Diploma degree in Medical Engineering Industry: Medical / Hospitals Job Summary: We are seeking a detail-oriented and analytical Biostatistician to join our medical research and clinical team in Nashik. The role involves applying statistical methods to design, analyze, and interpret data from medical and healthcare studies to support evidence-based decision-making. Key Responsibilities: Design, develop, and implement statistical methodologies for medical and clinical research projects. Analyze biomedical data from clinical trials, laboratory research, or healthcare s...

Location Hyderabad, India Novartis is unable to offer relocation support for this role please only apply if this location is accessible for you About The Role Are you passionate about driving clinical trial excellence from the ground upNovartis Global Drug Development is seeking a dynamic Study Start-Up Lead to spearhead global SSU activities, ensuring timely site activation and regulatory submissions This is your opportunity to lead cross-functional teams and make a meaningful impact in global health innovation About The Role Key Responsibilities Lead global SSU planning and execution to enable timely site activation and regulatory submissions Configure and manage SSU systems including CTMS...

The Clinical Database Programmer is primarily responsible for LSH Setup and Data Loading activities (both Inbound and Outbound) with External Data providers Also provide support to manage the load, Transfer and conform Clinical Trial Data to Novartis Internal standards and the provision of Clinical Data extracts to Clinical Data Consumers of study-level or project level deliverables under minimal guidance About The Role Major accountabilities Contribute to LSH and Data Loading activities as Clinical Database Programmer for phase I to IV clinical studies in Novartis Global Drug Development Participate in the review of Data Transfer specification documents and provide comments if required Resp...

Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support These tasks are to be performed independently or team based with guidance and supervision About The Role Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders Facilitate interaction with en...

Assist in the timely & professional ongoing Mgmt of data Operations on Use Cases/Demand deliverables and of clinical data warehouse maintenance with respect to cost, quality and timelines within Clinical Pipeline team Ensure high quality data available for secondary analysis use Support content development and upgrade to training modules into engaging and interactive applications Follows data regulations and laws, data-handling procedures and data mapping guidelines Supports quality deliverables within Clinical Data Operations (DO) Manage data Load, Transfer from Novartis Clinical Data Lake and conform of Clinical trial data to SDTM/ADaM compliant standards within the Clinical Data Warehouse...

In this role you will lead an impactful deliverable across the pharma value chain from drug discovery to commercialization by leveraging Indepth understanding in business process and Generative AI About The Role Major accountabilities Domain Expertise Possess a knowledge across the end-to-end pharmaceutical value chain, including drug discovery, preclinical and clinical trials, regulatory affairs, pharmacovigilance, technical operations (manufacturing, supply chain, and quality assurance), and commercial operations (market access, sales, and marketing), to lead AI-driven initiatives, Stay updated on advancements in Generative AI and their applications to optimize processes across the pharmac...

UNITTAS HOSPITALS IS A MULTISPECIALITY HOSPITALS

You will strategically and tactically support the Director Clinical Data Standards by advising and leading the planning, development, and implementation of Industry compliant, high-quality clinical data standards, infrastructure, or automation technologies. Your responsibilities will include providing expert support and excellent customer focus to business users and teams on various aspects such as data standard collection tools, data transfer specifications, analysis data standards, automation solutions, and business infrastructure. Additionally, you may lead global teams. - Ensure alignment with the CDS strategy - Plan, define, develop, validate, and support Clinical Data Standard/automati...

Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries May also provide statistical support to research or other R&...

Location Mumbai / Hyderabad, India Novartis is unable to offer relocation support for this role please only apply if this location is accessible for you, About The Role As the Clinical Research Medical Advisor (CRMA), your responsibility lies within the development of Global Clinical Trials this includes medical oversight for all trials, portfolio and/or protocol medical feasibility, scientific engagement of investigators, protocol and TA training for internal and external stakeholders, medical issue or question management, safety review, strategic input in pre-launch planning, You will drive compliance across all aspects of clinical trials and CRMA related activities It will be critical to ...

Location Mumbai / Hyderabad, India Novartis is unable to offer relocation support for this role please only apply if this location is accessible for you, About The Role As the Clinical Research Medical Advisor (CRMA), your responsibility lies within the development of Global Clinical Trials this includes medical oversight for all trials, portfolio and/or protocol medical feasibility, scientific engagement of investigators, protocol and TA training for internal and external stakeholders, medical issue or question management, safety review, strategic input in pre-launch planning, You will drive compliance across all aspects of clinical trials and CRMA related activities It will be critical to ...

Step into a role where innovation meets impact As a Digital Endpoint Expert, youll be a key member of the Digital Endpoint Capability Centre, driving the coordination, implementation, and deployment of digital endpoints and digital health technologies across clinical trials Youll bridge digital health expertise and clinical trial excellence, working closely with trial teams and cross-functional stakeholders to ensure seamless delivery Your leadership will shape the integration of novel measures across the development organization, while your expertise will help define implementation strategies tailored to each indication and trial design If you're passionate about digital health and ready to...

As a Protocol Review Specialist, you will play a crucial role in the clinical trials process. Your responsibilities will include reviewing protocols, responding to queries and clarifications from EC/IRB, answering medical questions, attending drug safety meetings, reviewing AE/SAEs, and providing protocol training to site staff, CRAs, etc. during investigator meetings. Key Responsibilities: - Reviewing protocol and providing suggestions to enhance the process - Responding promptly to queries/clarifications from EC/IRB - Addressing medical questions from sites or project teams effectively - Attending important drug safety meetings and external meetings - Thoroughly reviewing and documenting A...

As a Clinical Researcher at Clinikally, you will spearhead key areas of clinical research focused on the science behind consumer health solutions. You will collaborate with clinical partners globally to conduct efficacy studies on various OTC and Rx-grade products in dermatology and nutrition. Some specific 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 - Partner with clinical collaborators for efficacy studies on a range of products - Research consumer health solutions such as the Hyaluronic acid serum, Vitamin C S...