Clinical Research jobs in Centurion

We are looking for a Clinical Research Specialist with the following key knowledge areas: - Basic understanding of evidence-based medicine. - Knowledge of health data standards. - Knowledge of “managed healthcare” or financial risk assessment principles (environment). - Knowledge of standards within the health industry. - Knowledge of the legislation governing company, policies and procedures. -...

Job Description We are seeking a Recruiter 2, to join our DSSM Talent Acquisition team at IQVIA. This is a fully remote opportunity based anywhere in South Africa, but if you prefer a hybrid work arrangement, working in our offices is also an option. Job Overview Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an...

We provide meaningful careers that connect people with purpose. We are united by a common purpose of providing the best and safest care; and by our shared values of Care, Truth, Participation, Compassion and Dignity. Netcare invites you to be part of our journey. KEY WORK OUTPUT AND ACCOUNTABILITIES CONSISTENCY OF CARE Research activities • Active involvement in research activities to discover...

Introduction Through our client-facing brands Momentum Group, with Multiply (wellness and rewards programme), and our other specialist brands, including Guardrisk and Eris Property Group, the group enables business and people from all walks of life to achieve their financial goals and life aspirations. We help people grow their savings, protect what matters to them and invest for the future. We...

Role Purpose Provide senior specialist leadership for the Clinical Policy and Governance function within Health Risk Management by ensuring robust, evidence-based clinical policy, regulatory interpretation, and coding standards. The role is responsible for guiding health technology assessment, PMB and statutory interpretation, and clinical coding frameworks to inform benefit design, risk...

Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is...

Job Description We are seeking a recent graduate from a reputable South African institution to join our clinical research team as a Clinical Research Graduate. The role provides a multi-disciplinary supportive function to all teams in GCTO SSA. Examples include assisting in team meetings, supporting Site Ready dates, taking ownership of select processes within GCTO (such as the Onboarding...

Responsibilities include supporting end-to-end product development (formulation, design controls, validation, documentation, and transfer to production) as well as maintaining existing products to ensure quality, stability, safety, and regulatory compliance in a GMP/ISO 13485 environment. The role involves both collaboration with internal teams and independently managing workstreams. Independent...

Position Overview: The successful candidate will be responsible collecting, analysing and interpreting complex healthcare data to support clinical, operational and strategic decision-making. The role requires strong technical expertise in SQL, data visualisation tools such as Power BI (or similar) and knowledge of clinical coding standards. Essential Job Functions: - Extract, manipulate and...

Research AudiologistINTRODUCTION:An exciting opportunity has become available within the medical research industry, for a Research Audiologist. Our client is an impact-driven digital health company passionate about affordable access to healthy hearing for everyone, everywhere. This is an opportunity to be part of making a change and impacting human lives.The position is based in PretoriaJOB...

Parexel are currently recruiting for Senior UAT/Clinical Data Analysts in South Africa.In this role, the successful individuals will independently perform/lead and/or coordinate all clinical data validation activities on assigned projects, with a high degree of proficiency and autonomy. Further responsibilities shall include providing technical expertise and/or operational leadership regarding...

Role Purpose Ensure accurate and compliant underwriting decisions through thorough investigation, alignment with guidelines, analysis of underwriting criteria, and maintaining quality and compliance standards. Requirements - Underwriting Certification is advantageous. - Bachelor degree or equivalent qualification in a relevant field such as healthcare administration, nursing, allied sciences,...

Brief Description of Position:Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The role is critical to meet...

Base level role - 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, Database Lock and...

IQVIA is growing Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests IQVIA is seeking experienced Clinical Data Management Leads to oversee...

Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered. Job Overview Clinical Trial Managers (CTM) are an integral part of clinical trial delivery, leading and...

Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare...

Base level role 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, Database Lock and...

Job Overview Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from...

Advance level role Provide timely status updates including issues & risks to DM and DMLs as needed Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations May communicate with the vendors to resolve reconciliation issues. Provide input to Study set up activities including but not limited to creation of DVRs Create and/or provide...