Clinical Data Coder, Sponsor-dedicated

4 days ago


Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

Job Overview

Home-based in South Africa

The Clinical Data Coder will manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer's satisfaction; provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs; provide leadership to the team in the area of coding, project planning and execution, financial management, communication and milestone tracking. You may perform the role of a Data Operations Coordinator (DOC), Data Team Lead (DTL), and a customer site lead or may be responsible for managing and delivering a program of studies for a customer.

Essential Functions

  1. Serve as an account lead, or internal or external point of contact on standalone coding studies or accounts.
  2. Manage the customer relationship for the project team including active participation in coding related customer negotiation on timeline, budgetary and other issues.
  3. Provide leadership and senior support to lead coders on one or more large global studies.
  4. Manage the relationship with a customer on a DM site level.
  5. Serve independently as a Lead Data Coder and/or Coding reviewer for one or more projects.
  6. May serve as a DOC or DTL for one or more projects.
  7. Perform comprehensive quality control procedures.
  8. Perform Serious Adverse Event (SAE) reconciliation activities.
  9. Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks.
  10. Proactively identify, solve quality issues and deliver projects as per agreed timeline.
  11. Identify and provide due diligence for out of scope activity.
  12. Manage resource capacity for the project team.
  13. Mentor other team members in training and developing coding expertise.
  14. Independently bring project solutions to the Coding and CDM team.
  15. Identify and implement processes and quality improvement initiatives in the DM and coding function.
  16. Developing and implementing best practices in the team.
  17. Manage the development and implementation of new technologies.
  18. Demonstrate scientific and research temperament by presenting at, or participating in local and international forums.
  19. Responsible for identifying and implementing process improvements using established methods (principles of lean and six sigma) in collaboration with experts.
  20. Provide review and expert opinion in developing, revising, and maintaining standard core operating procedures and work instructions.
  21. Perform other duties as directed by the DOC, DTL or Manager, or meet objectives as assigned.
  22. Develop and maintain good communications and working relationships with the CDM team and client stakeholders.

Qualifications

  1. High School Diploma or equivalent Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent Pref.
  2. 7 years (advanced role) or 3/4 years (base role) in clinical trials within a similar function, including proven competence in managing the delivery of coding or/and other data management processes for multiple global projects, also including experience in handling complex customer negotiations and bid defense meeting. Pref.
  3. Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.).
  4. Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology required for many tasks.
  5. Advanced knowledge of data management processes and systems and advanced ability to apply this knowledge in practice.
  6. Excellent understanding of clinical drug development process (detail oriented).
  7. Outstanding communication and organizational skills.
  8. Proven leadership skills.
  9. Good project management skills related to all phases of clinical studies.
  10. Excellent knowledge of operating procedures and work instructions and the ability to apply them in practice.
  11. Excellent English written and oral communication skills.
  12. Ability to work on computer systems with ease and good working knowledge of computer programs.
  13. Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems.
  14. Ability to establish and maintain effective working relationships with co-workers and managers.
  15. Comprehensive understanding of financial management concepts and able to interpret the financial information.
  16. Able to present information effectively to individuals and groups.
  17. Able to make independent decisions within scope of authority and considers the impact of decisions on other groups and people.
  18. Able to motivate and lead teams to reach defined objectives.
  19. Effective team management skills including conflict resolution, delegation, and change management.
  20. Excellent interpersonal skills.
  21. Able to establish trust and collaborative relationships with customers.
#J-18808-Ljbffr

  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    About the RoleWe are seeking a highly skilled Clinical Data Coder, Sponsor-dedicated to join our team at IQVIA LLC. In this role, you will work closely with Study Data Managers to develop coding guidelines, deliver timely and accurate coding, and perform quality control checks.ResponsibilitiesDevelop coding guidelines in line with study requirements defining...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    Job DescriptionWe are seeking a highly skilled Clinical Data Coder, Sponsor-dedicated to join our team at IQVIA LLC. In this role, you will be responsible for managing single and multi-service projects, providing expert skills as part of a Clinical Data Management (CDM) team, and delivering timely, consistent, accurate, and reproducible coding.Key...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    Job SummaryClinical data coders play a crucial role in ensuring the quality and accuracy of clinical trial data. As a Clinical Data Coder, Sponsor-dedicated at IQVIA LLC, you will be responsible for managing single and multi-service projects, providing expert skills as part of a Clinical Data Management (CDM) team, and delivering timely, consistent,...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    Role OverviewIQVIA LLC is a leading provider of clinical research services, commercial insights, and healthcare intelligence. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments. As a Clinical Data Coder, Sponsor-dedicated, you will be an integral part of our team, working on various projects...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    About the RoleIQVIA LLC seeks a skilled Clinical Data Coder to manage single and multi-service projects, ensuring quality deliverables on time and to customer satisfaction.The successful candidate will provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs.Key Responsibilities:Serve as an...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    About the PositionWe are seeking a highly skilled Clinical Data Coder to join our IQVIA LLC team.The successful candidate will be responsible for managing single and multi-service projects, ensuring quality deliverables on time and to customer satisfaction.Key Responsibilities:Serve as an account lead for standalone coding studies or accounts.Manage the...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    About the JobWe are seeking a highly skilled Clinical Data Coder to join our IQVIA LLC team.The successful candidate will be responsible for managing single and multi-service projects, ensuring quality deliverables on time and to customer satisfaction.Key Responsibilities:Serve as an account lead for standalone coding studies or accounts.Manage the customer...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Clinical Data Management Project LeadIQVIA is a global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We're seeking an experienced Clinical Data Management Project Lead to join our team.Job Summary:You will be responsible for managing end-to-end delivery of data management services for...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Clinical Data Management ExpertiseWe are seeking an experienced Clinical Data Management Lead to join our team. As a key member of our Data Management department, you will play a vital role in managing end-to-end delivery of data management services for multi-service projects.Main Responsibilities:Leadership and Vision:Develop and maintain a positive and...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    About This OpportunityIQVIA LLC is seeking a talented Clinical Data Coder to manage single and multi-service projects.The successful candidate will provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs.Key Responsibilities:Serve as an account lead for standalone coding studies or...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    Clinical Data Associates at IQVIA LLC are responsible for ensuring the integrity and quality of clinical data. Key responsibilities include data review, query generation, data reconciliation, and study closeout activities.Required Skills and Qualifications:Bachelor's degree in a Health or Science discipline with experience in clinical research.Data...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution,...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution,...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    IQVIA: Leading Human Data ScienceIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We push the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.Data Management Lead RoleYou will be...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Job OverviewIQVIA Argentina is seeking a highly skilled Senior Clinical Research Associate to join our team. The ideal candidate will have extensive experience in clinical research and a proven track record of conducting monitoring and site management work.Conduct site visits to ensure that sites are conducting studies and reporting data as required by the...


  • Bloemfontein, Orange Free State, South Africa IQVIA LLC Full time

    Clinical Data Associate - Hybrid (Bloemfontein)Apply locations: Bloemfontein, South Africa; Cape Town, Western Cape, South Africa; Centurion, South AfricaTime type: Full timePosted on: Posted YesterdayTime left to apply: End Date: May 1, 2025 (30+ days left to apply)Job requisition id: R1468141Base level rolePerform comprehensive data management tasks...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Job OverviewIQVIA Argentina is seeking a skilled Clinical Data Management Lead to oversee the management of clinical trials.This role involves providing data management support, oversight and/or accountability for one or more clinical trials. The successful candidate will take the lead with trial customers and other internal and external partners to...


  • Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Lead Clinical Data Manager OpportunityIQVIA is a global leader in human data science, providing advanced analytics, technology solutions and clinical research services to the life sciences industry. We're seeking an experienced Clinical Data Management Lead to join our team.Job Summary:You will be responsible for managing end-to-end delivery of data...


  • Bloemfontein, Orange Free State, South Africa IQVIA Full time

    About the JobWe are looking for an experienced Clinical Data Manager to join our team at IQVIA. In this role, you will be responsible for managing and analyzing large datasets, developing and implementing eCRF and other data collection tools, ensuring data quality and integrity, and collaborating with cross-functional teams.Main Duties:Data Analysis: Analyze...

  • Senior Data Manager

    3 days ago


    Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

    Key ResponsibilitiesOversee the management of clinical trials, providing data management support, oversight and/or accountability.Work with trial customers and other internal and external partners to establish, align and confirm data management expectations.Create, plan and track content, format, quality and timing of data management deliverables.Perform...