635 Clinical Data Jobs - Page 12

As a Clinical Data Management (CDM) professional, you will be responsible for overseeing the full lifecycle of clinical data management processes. Your role will involve ensuring the quality and integrity of clinical trial data, developing and implementing data management plans, and monitoring data entry and validation processes. You will coordinate with clinical teams to ensure timely data collection and conduct data cleaning and review activities. Additionally, you will be preparing data for statistical analysis and reporting while ensuring compliance with regulatory requirements and industry standards. Participating in protocol development and study design, utilizing data management softw...

About The Role Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Analyst Qualifications: Master Degree in Life Sciences Years of Experience: 3 to 5 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 ...

Review and analyses ED medical records for completeness and accuracy. Assign ICD 10CM, CPT and HCPCS codes for diagnosis, procedures, and services provided in the ED Abstract clinical data for reporting, billing and quality improvement purposes and querying providers when necessary. Meet productivity and accuracy standards set by the department Stay updated on coding guidelines, Payer policies and regulatory changes Assist in reducing claim denials by ensuring correct and complete coding What you will need: Minimum of 2+ Years of Medical coding in ED Profee specialty is required AAPC or AHIMA is mandatory Any Graduation is required Must have good knowledge of medical terminology, ICD 10CM, C...

Review and analyses ED medical records for completeness and accuracy. Assign ICD 10CM, CPT and HCPCS codes for diagnosis, procedures, and services provided in the ED Abstract clinical data for reporting, billing and quality improvement purposes and querying providers when necessary. Meet productivity and accuracy standards set by the department Stay updated on coding guidelines, Payer policies and regulatory changes Assist in reducing claim denials by ensuring correct and complete coding What you will need: Minimum of 1+ Years of Medical coding in Multi-specialty Denials is required AAPC or AHIMA is mandatory Any Graduation is required Must have good knowledge of medical terminology, ICD 10C...

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Document...

Provide technical assistance as part of a team to develop and maintain clinical systems that meet internal and external clients needs. Assist with the development of database for local, regional, or transnational use. Assist in planning and coordinating database design, development, implementation, maintenance, and user support of clinical systems. Assist with programming, testing, and documenting databases in accordance with programming standards and validation procedures. Assist with programming database manipulations and transfers of data for internal and external clients. May assist IT in testing new upgrades to technologies. Understand and comply with core operating procedures and worki...

Skills and Experience that Will Help You Succeed Proven expertise coding and analyzing healthcare datasets to generate metrics based on real-world data Demonstrated ability to execute implementation requirements that include subsetting a large clinical database to a select set of patients that meet a number of criteria Ability to collaborate cross-functionally with teams (e.g., Commercial, Product, Medical, Engineering, etc.) to translate clinical investigation questions into programming logic Essential Requirements Masters or Doctorate in Engineering, Computer Science, Math, Statistics, or related quantitative field, or equivalent hands-on experience 3+ years of direct experience with healt...

Validation Manager is a client-facing role , supporting pharmaceutical and life sciences clients with the validation of the elluminate Clinical Data Cloud platform. This role is critical in ensuring clients achieve and maintain compliance with global regulatory requirements during the deployment and use of elluminate. As a trusted advisor, you will guide clients through validation planning, execution, and documentation, while ensuring alignment with best practices and industry standards. KEY TASKS & RESPONSIBILITIES Act as the primary validation subject matter expert (SME) during client implementations of elluminate. Provide strategic guidance to clients on Computer System Validation (CSV) a...

Position Overview We are seeking an experienced Senior Clinical Data Manager to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration between CTMS, EDC platforms, and clinical operations. Key Responsibilities CTMS Operations & Strategy Develop and maintain e-source, CTMS workflows, user roles, and system permissions. Ensure integration between CTMS and EDC systems for seamless data flow. Lead system upgrades, validation activities, and change control processes. Establish ...

Position Title: Photographer Activation Date: 28 July, 2025 Announced Date: 28 July, 2025 Expire Date: 08 August, 2025 Job Location: Badakhshan Nationality: National Category: Media-Journalism Employment Type: Full Time Salary: As per organization salary scale Vacancy Number: HHWO-47-2025 Of Jobs: 6 City: Faizabad Organization: Helping Hands for Women Organization HHWO Years of Experience: 3 Contract Duration: Short term Gender: Female Education: Bachelors degree in Photography, Visual Arts, Media & Communication, or a related field is required Close date: 2025-08-08 About Helping Hands For Women Organization HHWO HHWO, is a humanitarian non-profit, non-governmental, non-political, and non-p...

POSITION TITLE: Accounts & Receivables Associate DEPARTMENT: Finance Ora Values the Daily Practice of Prioritizing Kindness Operational Excellence Cultivating Joy Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world s leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past 45 years, our expert teams have helped earn more than 85 new product approvals. Oras pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 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&...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 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&...

Job Title - Research Investigator Job Location - Bangalore Department - Computational and Data Sciences (CDS) About Syngene Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical sectors. Syngene s 4500+ scientists offer both skills and the capacity to deliver great science, robust data management and IP security and quality manufacturing, at speed, to improve time-to-market and lower the cost of innovation. With a combination of dedicated research facilities for Amgen, Baxter, Bristol-...

About The Role Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 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 outcom...

As a(n) Senior Analytics Application Developer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Leading Creating healthcare analytics software solutions for HIS products and clients, collaborating within an agile team of engineers and developers Implementing Enterprise scale application, and reporting solutions. Determining the design, coding, and delivery of Solventum HIS products and customer solutions. Supporting Solventum HIS product development for customers across the US and the globe. Working closely with other teams to deliver our data driven products. Will...

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

- Collaborate with project managers to define scope, timelines, and deliverables - Ensure timely and effective execution of clinical trial software solution projects - Provide consulting for CTMS platform implementation, configuration Required Candidate profile - Advise on solution architecture, workflows, and usability enhancements in CTM systems - Validate the alignment of software features with clinical workflows and regulatory requirements Perks and benefits -GPA &term Insurance -5 days week -open to discuss

Role & responsibilities: Minimum 2 to 5 years of Experience with Clinical Data Management practices and relational database management software systems preferred. Strong background in conducting CDM activities. Must have experience in Conduct & Closeout, preferably in Inform EDC. Conduct Exp: Discrepancy Management, Vendor Recon, SAE, PK & PD, IVRS and lab, Data Cleaning, Manual data review. . Preferred to have startup experience Therapeutic area: Preferably Vaccine & Oncology Good to have Experience in CPT/Metrics Strong communication skills.

Build and maintain Power BI dashboards and data models for cross-functional business reporting. Develop and optimize data queries from the Enterprise Data Warehouse (EDW) and other systems. Normalize, transform, and integrate data to support both managed reporting and self-serve BI . Design reusable, governed datasets and provide training to help stakeholders adopt self-serve analytics confidently. Develop and maintain ETL workflows using Alteryx , Informatica , and MS Azure Data Factory . Apply advanced analytics and basic data science techniques for forecasting, costing, and workforce planning. Review work from junior analysts, provide coaching, and support enterprise data education initia...

Skill required: Clinical Data Services - Clinical eTMF Management Designation: Clinical Data Svs Associate Qualifications: BTech/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 outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: BTech/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 outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 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 outcomes by convergin...