53 Medical Data Collection jobs in South Africa
Clinical Data Risk Analyst
Posted 13 days ago
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Clinical Data Risk Analyst - Bulgaria, Sofia Hybrid: Office/Remote
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What you will be doingThe responsibilities of the Data Scientist include, but are not limited to:
- Identify data sources and propose data preparation approaches, e.g., using raw data sets as input
- Identify, select, and possibly combine key variables
- Prepare datasets based on specifications
- Set up and refresh Cluepoints reports (KRI, DQA) regularly according to study specifics
- Run additional analyses with B&P/TO teams to understand findings if appropriate
- Interpret findings to help RBM central monitors understand signals
- Prepare reports summarizing results, data findings, and signals
- Support the definition of actions to adapt RBM strategies to signals
- Collaborate closely with RBM Central Monitors
- Follow RBM processes for global and local teams
- Mentor new RBM Data Scientists
- Systems: SAS EG, Rave, Cluepoint, Anaconda3
- Skills:
- Cluepoint: Experience with Cluepoint is highly valuable. Understanding of CluePoint's smart engine, testing for KRI sensitivity, and familiarity with KRI & DQA dashboards setup and refresh process.
- SAS: Develop programs based on reference code and KRI specifications from scratch.
- Python: Update parameters, execute, debug, and perform minor or major updates to programs.
- Translate natural language specifications into programming code for KRI.
Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.
In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:
- Annual leave entitlements
- Health insurance options
- Retirement planning options
- Global Employee Assistance Programme through TELUS Health
- Life assurance
- Optional benefits like childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, etc.
Visit our careers site to learn more about our benefits.
ICON values inclusion and belonging, providing an accessible environment for all candidates. We are committed to equal employment opportunities and a workplace free of discrimination and harassment.
If you require reasonable accommodations during the application process or to perform job functions, please let us know or submit a request here .
Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly the candidate we're seeking.
If you are a current ICON employee, please click here to apply.
#J-18808-LjbffrClinical Data Manager (CDM)
Posted 17 days ago
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My client, a growing CRO is seeking a CDM (Clinical Data Manager) to be based in Bloemfontein.
Excellent salary and growth opportunities
The Clinical Data Manager (CDM) is responsible for maintaining and constantly improving the CRO’s performance and quality in data management services. This includes but is not limited to the following activities: Database set-up, maintenance and close-out activities for EDC and paper studies and development of data management-relevant study documents. Responsibilities also include supporting other (data management) team members, project management activities and communication with customers as well as process improvement.
Clinical data visualization expert
Posted today
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Clinical data risk analyst
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Clinical data visualization expert
Posted today
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Clinical data risk analyst
Posted today
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Online Data Research - Remote with Bonus!
Posted 1 day ago
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Be among the first 25 applicants
Job Description
Looking for a freelance opportunity where you can make an impact on technology from the comfort of your home? If you are dynamic, tech-savvy, and always online to learn more, this part-time flexible project is the perfect fit for you!
A Day in the Life of a Personalized Internet Assessor:
In this role, you'll analyze and provide feedback on texts, pages, images, and other types of information for top search engines, using an online tool.
Through reviewing and rating search results for relevance and quality, you'll help improve the overall user experience for millions of search engine users, including yourself.
Join our team today and start putting your skills to work for one of the world's leading search engines.
The estimated hourly earnings for this role are $14 USD per hour.
TELUS Digital AI Community
Our global AI Community is a vibrant network of over 1 million contributors from diverse backgrounds who help collect, enhance, train, translate, and localize content to build better AI models. Become part of our growing community and make an impact supporting machine learning models for some of the world's largest brands.
Qualification Path
No previous professional experience is required, but passing basic requirements and a standard assessment process are necessary. This is a part-time long-term project with quality assurance checks during the contract.
Basic Requirements
- Freelancer with excellent communication skills in English
- Resident in the US for the last 3 consecutive years, familiar with current and historical US business, media, sports, news, social media, and cultural affairs
- Active use of Gmail and social media, experience navigating web content
- Daily access to broadband internet, a smartphone (Android 5.0, iOS 14 or higher), and a personal computer
Assessment
Applicants will complete a language assessment, an open book qualification exam, and ID verification. Guidelines and learning materials will be provided. The exam must be completed within a specific timeframe at your convenience. Successful candidates will earn a $150 bonus if they pass the exam, verify their identity, and submit all required documents within 7 days, and stay active for at least 3 months.
Equal Opportunity
All qualified applicants will be considered regardless of race, color, religion, gender identity, national origin, disability, or veteran status. We are committed to diversity and inclusion, basing decisions on qualifications, merits, and performance.
Senior Level- Entry level
- Part-time
- Information Technology
- Technology, Information and Internet
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Online data research - remote with bonus!
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Senior Clinical Data Science Programmer
Posted 1 day ago
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As a Rave Database Developer, you will join the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing:
- Develop and maintain data management documentation and guidelines in accordance with Good Clinical Practices (GCP) and Good Documentation Practices (GDP).
- Provide subject matter expertise to project team members during all phases of the project lifecycle.
- Develop, test, and maintain data management systems.
- Assist during internal and external audits and inspections with your expertise.
- Collaborate with Data Managers, Study Teams, Vendors, and Site Staff to formulate Data Transfer plans for secondary data sources (e.g., Lab data, Site data).
- Batch import agreed data sources into the EDC system.
- Develop, program, validate, and maintain Medidata Rave EDC clinical trial databases according to company standards.
- Create EDC design specifications including data dictionary, event definitions, electronic consent, branching logic, edit checks, query rules, calculated fields, and dynamic forms.
- Design and construct the EDC database based on global eCRF libraries in collaboration with Data Managers and study teams.
- Configure and optimize patient interfaces for various data collection modes (eCOA on mobile devices or tablets, EDC on laptops/desktops).
- Conduct, test, and produce activities related to Rave EDC Migration.
- Develop test scripts and coordinate user acceptance testing (UAT) to ensure database accuracy.
- Manage deployment of new or updated EDC databases into production.
- Assist in mapping the EDC database to the enterprise data warehouse.
- Develop and implement standards to improve quality and streamline database build processes.
- Be available to work on any BSC studies.
- Follow BSC SOPs/WIs.
You are:
- Possessing 5+ years of experience in development.
- Metadata Rave certified (REQUIRED).
- Holding a BS Degree.
- Medidata Rave EDC Certified Study Builder.
- This is a hybrid position requiring 3 days on-site and 2 days remote in Marlborough, MA.
Candidates must be certified and have either:
- Medidata Rave EDC Certified Study Builder, or
- At least the equivalent experience with Medidata Rave Study Design and Build Essentials (SDBE).
Pay Range: $75,809 - $94,550 USD per year. Actual compensation depends on location, experience, education, and skills.
What ICON offers:
We prioritize a diverse culture that rewards high performance and nurtures talent. Besides a competitive salary, we offer benefits focused on well-being and work-life balance, including:
- Various annual leave entitlements
- Health insurance options
- Retirement planning
- Global Employee Assistance Programme
- Life assurance
- Optional benefits like childcare vouchers, gym memberships, and more
Learn more at:
ICON values inclusion & belonging. We are committed to an accessible environment and equal opportunity employment. If you need accommodations during the application process, please let us know through this form .
If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for!
#J-18808-LjbffrClinical Data Manager (Data Review)
Posted 13 days ago
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The Clinical Data Manager (CDM) will perform scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).
Deliverables:
- Services rendered will adhere to applicable Client SOPs, WIs, policies, local regulatory requirements, ICH-GCP, etc.
- Provides scientific data review support for more than one low to moderate complexity trial or one high complexity trial.
- The data management expert, within the therapeutic area, performs scientific (complex) clinical data review in close collaboration with SRP and SRS, leveraging technical and clinical expertise. Collaborates with SRP, SRS, Data Management, and other study team members to implement data management activities, focusing on complex indication and therapy-related elements. Reviews data flows, Data Management Plans, and performs continuous complex data review activities.
- Involved in study activities from protocol design, providing input into data collection tools.
- Reviews scientific study data, manages CDM and SRS/SRP queries in eDC system, and discusses findings with SRS/SRP. May be involved in coding and SAE reconciliation. Leads or attends meetings as appropriate.
- Leads collaboration with SRP/SRS and GDM to establish and confirm scientific clinical data review expectations for assigned trials.
- With trial stakeholders, reviews eCRF content, establishes data conventions and quality expectations, and sets timelines for CDM milestones.
- Creates the Integrated Review Plan, ensuring quality, scientific content, clarity, accuracy, and regulatory compliance. Reviews related documents.
- Ensures inspection readiness of all deliverables; participates in inspections and audits as necessary.
- Plans, tracks, and ensures timely delivery of CDM activities.
- Collaborates with SRS/SRP to meet trial needs and deliverables.
- Identifies lessons learned, best practices, and FAQs at the trial level.
- Participates in process, system, and tool improvement initiatives within clinical data management.
Therapeutic Area: Oncology, Cardiovascular, and Immunology
Education/Experience:
- BS/BA degree or higher in Health Sciences or related field, or equivalent professional clinical experience.
- At least 5 years of Data Management experience, preferably including clinical data review and knowledge of medical terminology.
- Experience collaborating with clinical teams.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create connections to accelerate the development and commercialization of medical treatments to improve patient outcomes and population health worldwide. Learn more at .
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