426 Clinical Data Jobs - Page 17

About The Role Skill required: Clinical Data Operations - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: MSc/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve o...

About The Role Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/BSc Years of Experience: 7 to 11 years Language - Ability: English(Domestic) - Intermediate What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life...

About The Role Skill required: Clinical Data Operations - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: MSc/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve o...

Role & responsibilities Handle, organize, and maintain clinical, medical, and healthcare project documentation. Accurately enter and validate healthcare and research data in internal systems. Review medical case records, lab reports, and related documentation for completeness. Collaborate with research, operations, and regulatory teams to gather required information. Prepare, format, and update reports for ongoing research and healthcare projects. Track timelines for documentation deliverables in line with project schedules. Maintain data confidentiality and adhere to industry compliance standards. Assist in the preparation of records for audits, inspections, and submissions. Perform quality...

We are looking for a highly skilled Medical Data Abstractor with 2-4 years of experience to join our team in Bengaluru. The ideal candidate will have a strong background in medical data abstraction and analysis, with excellent analytical and problem-solving skills. Roles and Responsibility Accurately and efficiently abstract medical data from various sources. Analyze and interpret complex medical information to identify key trends and patterns. Develop and maintain databases and systems to support medical data management. Collaborate with cross-functional teams to ensure data quality and integrity. Identify and resolve discrepancies or errors in medical data. Provide training and support to ...

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/MCA Years of Experience: 7 to 11 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertica...

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Sr Analyst Qualifications: BE/BTech/MCA Years of Experience: 5 to 8 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical...

The Position The Statistical Monitor plays a critical role in supporting Risk-Based Monitoring within Clinical Drug Development by operating and maintaining the centralized Statistical Monitoring function. This position focuses on detecting unusual data patterns, systematic errors, and potential instances of non-compliance or fraud that may not be identified through routine monitoring processes. The Statistical Monitor analyses clinical data across trials and projects to safeguard data integrity, which is essential for the approval of new drug. The role requires a high level of independence, with the potential to mentor junior colleagues and contribute to continuous improvement in data relia...

Role & responsibilities Should be responsible and have a good attitude. Must have good written and communication skills in English and Malayalam. Desire to work in a fast-paced, entrepreneurial environment. Should be a fast learner and ready to work on any modules. As a Business System Analyst, you will analyze user needs and data to generate concepts, create prototypes, and iteratively improve solutions. Develop mock-ups and user requirements that IT and technical teams can use to build or enhance solutions. Collaborate with cross-functional teams to gather required data, interpret analysis insights, and explore potential solutions. Document, translate, and communicate findings effectively ...

Project Name :- Use of Multi-omics approaches to understand auto inflammatory disorders (AID) and identify targets for precision medicine" Name of the Post :- Senior Project Assistant No. of Vacancy :- 01 Emoluments :- 30,600/- p.m. Essential Qualification :- Graduate in Life Sciences/Biochemistry/ Microbiology/Biotechnology/Bio-informatics from a recognized University with three years work experience from recognized Institute. Desirable Qualification :- M.Sc. In Life Sciences/Biotechnology. Experience in molecular biology, Flowcytometry ELISA, experience of working in Clinical Lab knowledge of computer application & Data Management. Age limit :- The Upper age limit is 30 years. Duration :- ...

What you’ll do You will spearhead the design & implementation of various innovative solutions in the realms of clinical trial, data management, analytics and RBQM. As a solution leader, your role will involve strategizing, offering tech consultancy, conducting assessments, and overseeing technology projects as the solution leader. You will be engaging with clients to review clinical business processes, determining requirements, establishing user narratives, and delivering solutions that have significant impact. You will lead requirements gathering activities and collaborate with product owner to prioritize and groom the backlog to ensure appropriate level of detail is captured at the right t...

What you’ll do - You will design & implement various innovative solutions in the realms of clinical trial, data management, analytics You will work in designing common data model based on clinical standards like SDTM / ADAM/ I ISS/ ISE . You will work on designing safety data mart for cross study analysis and exploratory analysis You will work on building analysis ready datasets which serves various safety and exploratory use cases across clinical trials. You have experience of building usecases like safety signal detection, reverse translation research, combination therapy exploration As a solution lead, your role will involve planning, offering tech consultancy, conducting assessments,and ...

Looking for Trainer Who Provides Offline training on Clinical Data Management On Part time basis Provides training and monitors performance to ensure the team are operating at the highest level to design and deploy clinical databases. Required Candidate profile Should have Experience on clinical data management Entire Work Process EDC SAE Reconciliation. should have Experience on Softwares (Oracle Inform/ Mediidata Rave) Interested Contact - 9133469786

Major Accountabilities Provides DM support across multiple (4 or more) assigned trial(s). Acts as the Trial Data Manager for 1 trial in sequence where needed Provides feedback to assure well-developed databases and data validation setup and execution while making the best use of standards and best practices Supports the team through database build requirements and complete startup activities for study including: building the eCRF, completion guidelines, standard and simple rules, data validation plan and user acceptance testing (UAT); can lead a study in sequence under PCDM supervision. Set up and manages external data in accordance with protocol requirements, process and validation requirem...

Our Team: The Patient Safety & Pharmacovigilance (PSPV) aspiration is to be a cutting-age safety group, to enable Sanofi to optimize the benefit-risk of our therapies, so we can best serve our patients and consumers. The PV Regions group is an international, dynamic, and culturally diverse team dedicated to the safety of Sanofi products in regions/countries. The [Multi] Country Safety Head ensures that local PV activities are performed in compliance with the global/regional/local PV regulations and PSPV Quality Documents (QDs) to warrant safe and appropriate use of Sanofi products in the assigned country (or countries for the M-CSH). CSH Main responsibilities: The face of the Safety organiza...

Bachelors degree from reputable university preferably in science/ mathematics related fields Preferred SAS certification Technical Skills Requirements Must have expertise of SAS Base, and good knowledge of SAS graph and SAS Macros. Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician. Must have excellent knowledge of CDISC standards (SDTM and ADaM) Thorough understanding of relational database components and theory. Excellent application development skills. Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results. Good understanding of ICH E6, ICH E3, ICH E8, ...

Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulat...

We are looking for a passionate Applied AI Engineer to join our innovative team, focusing on the exciting field of Large Language Models (LLMs) in the context of Public Health . In this role, y ou will lead the design, fine-tuning, deployment, and evaluation of AI/ML systems based on pre-trained models (e.g., LLaMA, Mistral, GPT, Phi) that help ease the lives of healthcare workers and clinicians. You will work closely with back-end and mobile engineers to bring cutting-edge AI capabilities to life. The ideal candidate will possess the expertise to leverage existing Large Language Models (LLMs) to train and evaluate models using program-specific clinical data (e.g., patient notes, SMS interac...

Product Management at Innovaccer Our product team is a dynamic group of skilled individuals who transform ideas into real-life solutions. They mastermind new product creation, development, and launch, ensuring alignment with the overall business strategy. Additionally, we are leveraging AI across all our solutions, revolutionizing healthcare and shaping the future to make a meaningful impact on the world. Your Role We are seeking a Senior Product Manager to drive the 0-1 development of a new utilization management platform. You will manage the end-to-end product lifecycle: conceptualize, prioritize requests and requirements from multiple internal and external stakeholders, and drive product ...

Summary Supports Head CDS in setting the standards and automation strategy across Novartis. Manage a global team(s) responsible for executing data standards / automation objectives across DO. Responsible for ensuring quality, scalable, reusable, (CDISC and regulatory) compliant data standards and technologies are transparently deployed across GDO in close collaboration with external industry peers and internal stakeholders delivering stellar customer focus. Responsible for planning and overseeing KPIs/metrics, frameworks, policies, business rules and processes for development, maintenance, deployment. Responsible to ensure Novartis fulfills a ROI across the standards and automation landscape...

Job title: Data Steward Location: Hyderabad, India About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients daily life, wherever they live and enabling them to enjoy a healthier life. As a company with a global vision of drug ...

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of c...

Responsibilities: Develop and maintain strong relationships with KOLs, academic institutions, medical societies, and other relevant stakeholders in assigned therapeutic areas. Serve as a credible and trusted scientific resource for healthcare professionals, providing accurate and up-to-date information on our products, disease states, clinical data, and treatment guidelines. Identify and engage with potential investigators for company-sponsored clinical trials and support investigator-initiated research studies (IIS) by providing scientific and logistical support. Deliver scientific presentations and educational programs to HCPs, both individually and in group settings, to enhance understand...

Position Summary We are seeking a talented and driven Data Scientist to join our dynamic team at Illumina. In this role, you will collaborate with cross-functional teams of scientists, engineers, and bioinformaticians to analyze complex biological data, develop advanced models, and deliver actionable insights that propel Illumina s research, development, and commercial objectives. Your work will directly support initiatives across genomics, clinical applications, and product development, helping to shape the future of personalized medicine and health care. Key Responsibilities Design, develop, and implement robust statistical models, machine learning algorithms, and analytical pipelines. Par...

Position Summary We are seeking a talented and driven Data Scientist to join our dynamic team at Illumina. In this role, you will collaborate with cross-functional teams of scientists, engineers, and bioinformaticians to analyze complex biological data, develop advanced models, and deliver actionable insights that propel Illumina s research, development, and commercial objectives. Your work will directly support initiatives across genomics, clinical applications, and product development, helping to shape the future of personalized medicine and health care. Key Responsibilities Design, develop, and implement robust statistical models, machine learning algorithms, and analytical pipelines. Par...