174 Data Review Jobs - Page 3

You will be responsible for assisting in the design, review, and testing of Case Report Forms (CRFs) and electronic data capture (EDC) systems. Your role will involve supporting data entry, review, and cleaning activities under the guidance of senior data managers. Additionally, you will perform data validation and run basic edit checks to identify discrepancies. Key Responsibilities: - Assist in the design, review, and testing of Case Report Forms (CRFs) and electronic data capture (EDC) systems - Support data entry, review, and cleaning activities under the guidance of senior data managers - Perform data validation and run basic edit checks to identify discrepancies - Help create and maint...

SUMMARY This is a remote position. Contour Education is seeking a Sales Auditor - a detail-oriented and process-driven professional who ensures that all sales activities and trial bookings meet company standards for accuracy, documentation, and compliance. You will work closely with the Sales Manager to review sales communications, CRM records, and booking data, ensuring that every action aligns with Contour’s defined procedures and policies. Your work will directly strengthen accountability, improve operational efficiency, and uphold Contour’s commitment to transparency and quality in every sales interaction. This role is ideal for someone who enjoys structured review work, precise document...

JOB DESCRIPTION: Represents Data Management as the clinical database and data management subject matter expert on Clinical Project Teams through the following: . Attend Clinical Project Team meetings to gather business need requirements and translate to technical requirements . Partner with other shared service functions such as Safety, Core Lab, etc. to gather business need requirements and translate to technical requirements . Identify, analyze, propose solutions, and effectively resolve complex data issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions . Train database End Users (internal and external users) o...

Responsible for Overall site QA compliance activities and drive the organization towards quality improvements Handling of Deviation, Change controls, OOS, OOT and CAPA including investigations and impact assessments

What We Are Looking For We are seeking an experienced Clinical Data Manager (CDM) / Lead Clinical Data Manager to joinour growing clinical data management team. The ideal candidate will have a strong background inend-to-end data management, EDC systems (preferably Medidata Rave, Veeva, InForm/CD orsimilar), and experience leading or mentoring data management teams. This role will be office-based in Gurugram, with close collaboration with leadership and cross-functional teams to ensuredata integrity, compliance, and quality throughout clinical studies. What You'll Do Manage and oversee all aspects of clinical data management (CDM) activities for assigned clinicalstudies. Develop and review Da...

Review and analyze health data to ensure accuracy and compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve data discrepancies.Develop/implement effective data review processes to improve quality Required Candidate profile Strong understanding of employment firms and recruitment services.Excellent analytical and problem-solving skills, with attention to detail and the ability to work independently.

Review and analyze health data to ensure accuracy and compliance with regulations.Identify trends and patterns in health data to inform business decisions.Collaborate with cross-functional teams to develop and implement data-driven solutions. Required Candidate profile Strong understanding of health data principles and regulations.Experience with data analysis and interpretation techniques.Excellent communication and collaboration skills.

Review and analyze health data to ensure accuracy and quality.Identify trends and patterns in health data to inform business decisions.Collaborate with cross-functional teams to develop and implement data-driven solutions. Required Candidate profile Strong analytical and problem-solving skills are required, along with attention to detail and the ability to interpret complex data.Excellent communication and interpersonal skills

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in the ECR system.Collaborate with cross-functional teams to resolve issues Required Candidate profile Strong understanding of ECR systems and data analysis principles. Excellent analytical and problem-solving skills with attention to detail.

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in the ECR system.Collaborate with cross-functional teams to resolve issues Required Candidate profile Strong understanding of ECR systems and data review principles. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a fast-paced environment

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in ECR data to the relevant team.Develop and implement effective data review Required Candidate profile Strong understanding of ECR data principles and practices. Excellent analytical and problem-solving skills, with attention to detail.

Conduct thorough reviews of clinical data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Required Candidate profile Strong understanding of clinical data review principles and practices. Proficiency in data analysis and interpretation software.

Conduct thorough reviews of clinical data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Required Candidate profile Strong understanding of clinical data management principles and practices. Proficient in using relevant software and tools for data review and analysis.

Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Required Candidate profile Strong understanding of clinical trial design, protocols, and regulatory requirements. Proficiency in data review software and tools, such as Excel, Word, PowerPoint, or statistical analysis software

Conduct thorough reviews of clinical data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Develop and implement effective data management strategies Required Candidate profile Strong understanding of clinical data review principles and practices. Excellent analytical and problem-solving skills with attention to detail. Effective communication and interpersonal skills

Conduct thorough reviews of ECRF data to ensure accuracy and compliance with regulatory requirements. Identify and report any discrepancies or issues found during data review. Collaborate with cross-functional teams to resolve data-related issues. Required Candidate profile Strong understanding of ECRF data management principles and practices. Excellent analytical and problem-solving skills, with attention to detail.

Role Overview: As a Clinical Data Coder 1, you will be responsible for providing comprehensive data management expertise to the Data Management team in order to meet sponsor and company needs. You will perform Clinical Data Management and/or Coding activities, and may also provide leadership in roles such as Lead Coder or Data Operations Coordinator (DOC) for specific CDM tasks. Key Responsibilities: - Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols. - Manage delivery of coding activities and/or stand-alone coding projects throughout the full study life-cycle with minimal guidance. - Validate/test the coding application and programming of codin...

Role Overview: As a Recovery and Resolution Planning Specialist at Deutsche Bank, you will play a crucial role in ensuring compliance with US and Global regulations by creating and maintaining Contingency Strategy (CS) documents for material relationships with Financial Market Infrastructures (FMIs) and Agent Banks. Your responsibilities will involve coordinating annual data collection, interpreting regulatory guidance, engaging with various internal functions, and managing the creation and review of CS documents. Key Responsibilities: - Support the completion of the annual data gathering outreach, including validation and review of data. - Analyze and interpret regulatory guidance to enhanc...

Annotate Chemistry-related data to improve AI comprehension. Provide feedback on AI-generated responses to ensure scientific accuracy. Assist in developing problem sets and solutions for AI training. Collaborate with AI researchers to refine AI capabilities in the field of Chemistry. Must Required Traits: Strong academic background in Chemistry. Experience in Chemistry education, research, or content creation preferred. Familiarity with AI, machine learning, or data annotation is a plus. Excellent problem-solving and analytical skills.

As a Centralized Clinical Trial Manager at ICON, you will be responsible for leading the centralized monitoring activities for clinical trials to ensure trial quality and patient safety. Your key responsibilities will include: - Leading the centralized monitoring activities for clinical trials, including data review and risk-based monitoring. - Collaborating with clinical operations, data management, and biostatistics teams to identify potential risks and ensure proactive management of trial data. - Ensuring study compliance with regulatory requirements and protocols by overseeing real-time data reviews and monitoring activities. - Providing oversight on site performance, patient safety, and...

As a Senior Clinical Data Co-ordinator, your role will involve overseeing and co-ordinating tasks delegated to the study team members. You will be responsible for providing training to new data management personnel on data management processes and procedures. Your key responsibilities will include: - Planning, managing, controlling, and performing data processing and management activities for assigned projects in a timely and accurate manner, adhering to trial Sponsors requirements. - Creating and developing study specifications, implementing, testing eCRF or paper CRF edit checks, and conducting data review and overview listings. - Authoring and reviewing the Data Management Plan (DMP) and ...

- Understand and follow study start-up, conduct, and close out activities per the standard process, which will be made known to Service Provider and to the Data Manager in advance and in writing by Baxter. - Act as a single point of contact from the Service Provider for the studies as assigned - Prepare/review eCRFs, Edit checks, and Custom Functions requirement document - Prepare or review edit checks requirement and functional test script document - Perform functional testing for eCRF/edit checks and Custom Functions - Identify reports and DM Tables requirements and prepare a report specification document - Review and provide feedback for study conduct activities performed by the Service P...

Job Title : Clinical Trail Administrator Function: R&D - Clinical Development Job Location : Corp. Office, Jubilee Hills, Hyderabad Role & responsibilities 1. Assist with the Ethics / Regulatory Submissions; keep a track of submissions & approvals for the study. 2. Help medical team in preparing Protocols, Investigator Brochures and CRFs which includes keeping track and re-ordering supplies. 3. Set up and maintenance of the Trial Master Files (TMF) or Electronic filing systems/ set up of the Investigator Site File (ISF)/Site Master Files (SMF). 4. Managing and maintaining study documents & trial supplies e.g.; Patient/subject Information Sheets, Patient/subject Diaries, Source document templ...

Role Overview: You will provide expert support and functional and technical knowledge to ensure the scientific integrity and validity for clinical development, early development, and/or research projects. You will participate in the full lifecycle of producing key data and/or reports, including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities, and provide quantitative analytical support. Additionally, you will provide statistical support for regulatory submissions, planning, analysis, and reporting of clinical safety and efficacy summaries. You may also provide statistical support to research or othe...

As a SAS Programmer at Precision for Medicine, you will play a crucial role in supporting the success of clinical trials through your SAS programming skills. Your responsibilities will include: - Developing and maintaining SAS programming to support the review of clinical data as part of a cross-functional data review and cleaning approach - Providing collaborative input to design SAS outputs for metrics, reconciliation reports, tools, listings, and standard patient profiles - Supporting the development of complex proprietary patient profiles for efficient data review and monitoring - Ensuring on-time delivery of projects, communicating project status to internal teams - Developing, testing,...