28 Research Study jobs in South Africa
Research Study Coordinator
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Research Study Coordinator page is loadedResearch Study Coordinator Apply locations Kwazulu-Natal time type Full time posted on Posted 7 Days Ago time left to apply End Date: August 30, 2025 (4 days left to apply) job requisition id JR100562
Description:
Overview of Duties:
AHRI is looking for a Research Study Coordinator who will be based at our Mtubatuba, Somkhele site in KwaZulu-Natal, South Africa. The successful candidate will be responsible for the implementation of the ATTIS project conducted at AHRI Somkhele in Mtubatuba, Richards Bay, Empangeni and surrounding areas. Responsibilities include leading and coordinating clinical team working on the ATTIS TB study and ensuring TB case finding. The appointed candidate will be responsible for ensuring that the project clinical governance standards are met in line with Good Clinical Practice guidelines. The incumbent will be responsible for managing the day-to-day activities of the project by ensuring that all aspects-from recruitment to data collection to analysis-are handled in an efficient and effective manner. This will be done under the guidance of the PI, project manager/research associate and other project management team. The position will be based primarily in our Somkhele site.
Overview of duties:
- Develops, maintains, and manages appropriate study documentation in line with guidance including ICH-GCP, applicable regulatory requirements, and relevant SOPs.
- Organizing and managing project schedules, including setting milestones and deadlines for team members to ensure that projects are completed on time.
- Coordinating with study participants to ensure compliance with the study protocol.
- Coordinating with members of other departments to ensure that all tasks are completed successfully.
- Managing budgets by tracking expenses and requesting additional funds if needed.
- Implement core research protocol and associated research studies.
- Work in a multidisciplinary team and liaison with Department of Health and other key stakeholders to ensure good partnership between AHRI DOH and stakeholders.
- Support the programme manager/Research Associate to monitor the progress of the project, ensuring timely delivery of milestones.
- Attend and take minutes in weekly meetings with clinical staff.
- Prepare clinical reports.
Minimum Qualifications:
- Must have obtained Nursing Degree or other Clinical degree; or BSc degree, or related, preferably in Life Sciences.
Minimum Experience:
- A minimum of 2 - 3 years' experience coordinating a project and supervising junior staff members.
- A valid driver's licence and must have been driving longer than 2-years.
- Good Clinical Practice (GCP) certification is an added advantage.
Skills Required:
- Good verbal and written communication skills in English.
- Accuracy and precision.
- High computer literacy.
- Report writing.
- Must be able to work under pressure.
- Ability to document information accurately, methodically and pay attention to detail.
- Ability to work independently and show initiative.
- Excellent organizational, coordination and leadership skills.
- Must be able to show good interpersonal skills.
Worker Type:
EmployeeThe application closing date:
30 Aug 2025Please note that only shortlisted candidates will be contacted, kindly consider your application as unsuccessful if you do not hear from us within 14 days of the application closing date.
Similar Jobs (1) Research Associate locations Kwazulu-Natal time type Full time posted on Posted 7 Days Ago time left to apply End Date: August 30, 2025 (4 days left to apply) About UsAfrica Health Research Institute’s vision is optimal health and well-being of under-resourced populations.
Africa Health Research Institute (AHRI) is an independent, transdisciplinary scientific research institute based across two campuses in the province of KwaZulu-Natal (KZN) in South Africa.
AHRI’s research combines population, basic and translational, social, and clinical sciences to understand and intervene in the health and well-being of South African communities.
AHRI works in partnership with local communities and South African academic, governmental, and other policy stakeholders and collaborates with over 60 institutions globally. AHRI prioritises the training of the next generation of African scientists.
The work lives of AHRI’s ~700 scientists, students and staff members are driven by our values: ubuntu, transformation, leadership, innovation, excellence and collaboration.
Developer, SAP S4 BPT Group Reporting and Data Collection
Posted 19 days ago
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Developer, SAP S4 BPT Group Reporting and Data Collection
Job Overview
Business Segment: Group Functions
Location: ZA, GP, Johannesburg, Baker Street 30
To design, code, test, debug, and maintain programs in development environments. Apply agreed standards and tools to achieve a well-engineered result. Work within a strict framework of programming standards under the supervision of senior technical resources.
Qualifications
- Degree in BSc Computer Sciences or BCom in Finance or Accounting
- Good Knowledge of Accounting and Financial Consolidations
- Must have at least 1 to 2 years of design and development experience in SAP Business Technology Platform Workflow Management Service or other workflow capabilities such as Power Automate
- Ideally must have 1 to 2 years’ experience working on SAP Group Reporting and Group Reporting Data Collection
- 3-4 Years’ development experience on SAP Business Warehouse
Developer, SAP S4 BPT Group Reporting and Data Collection
Posted 19 days ago
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Job Description
Developer, SAP S4 BPT Group Reporting and Data Collection
Job Overview
Business Segment: Group Functions
Location: ZA, GP, Johannesburg, Baker Street 30
To design, code, test, debug, and maintain programs in development environments. Apply agreed standards and tools to achieve a well-engineered result. Work within a strict framework of programming standards under the supervision of senior technical resources.
Qualifications
- Degree in BSc Computer Sciences or BCom in Finance or Accounting
- Good knowledge of Accounting and Financial Consolidations
- Must have at least 1 to 2 years of design and development experience in SAP Business Technology Platform Workflow Management Service or other workflow capabilities such as Power Automate
- Ideally must have 1 to 2 years’ experience working on SAP Group Reporting and Group Reporting Data Collection
- 3-4 years’ development experience on SAP Business Warehouse
Developer, sap s4 bpt group reporting and data collection
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Developer, sap s4 bpt group reporting and data collection
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Clinical Research Associate
Posted 13 days ago
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Our clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team in South Africa. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you.
We kindly ask to submit applications in English.
Entry level associates with research associate or trial assistant-type backgrounds may also be considered.
Responsibilities- Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up;
- Assess patient recruitment and retention.
- Minimum a Bachelor of science in health-related field or equivalent
- Minimum of 1-year independent clinical monitoring; Entry level associates may be considered with relevant trial assistant or research associate-type backgrounds
- Broad knowledge of medical terminology and clinical patient management
- Basic knowledge of drug therapy techniques and clinical research methodologies
- Comprehensive knowledge of Local Regulations and ICH GCP
- Excellent oral and written communication skills
- Fluency in English
- Great attention to detail
- Must hold a valid driver’s license
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
#J-18808-LjbffrClinical Research Project Manager
Posted 13 days ago
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The candidate will report to the Vice President of Research. Incumbent will manage all aspects of ongoing research studies. Attention to detail, self-starter, well organized, as well as good communication skills are essential. The applicant must adhere to patient confidentiality. The individual will be responsible for the oversight of studies conducted out of the clinical trials unit, including contracts, overseeing the research coordinators, study progress reports, orders, and other tasks as needed.
Responsibilities- Monitor study metrics and site performance using standard study management tools.
- Oversee the individual study progress over the duration of each project.
- Act as the direct liaison between sponsors/investigators and the research coordinator or Vice President.
- Establish research data and workflow plans.
- Contribute to the development and implementation of SOPs, project-specific procedures, technical guidance documents, and patient acquisition plans.
- Direct the establishment of clinical and analytical study-related protocols and documents, as well as research/clinical data analysis.
- Manage the orders, sample deliveries, and supplies required for each study.
- Interface with investigational sites, clinical consultants, and labs.
- Manage research data sites and renewal terms related to each study and CTU functions.
- Direct all aspects of research data generation and analysis, including external site clinical studies and internal analytical studies.
- Drive internal communication, including timelines, budget, progress, and project needs for clinical trials to product teams and senior management.
- Interface with ORA, IRB, WMC, and other pharmaceutical/hospital research offices.
Education requirement: Bachelor's degree in biology, mathematics, computer science, natural sciences, or related areas.
Licenses or certifications: CITI certification.
Technical/Computer skills: Ability to use a combination of validated Electronic Data Capture (EDC) systems and/or other internal or commercial software tools and proven ability to learn and apply new software quickly as projects require. Familiarity with REDCap preferred. Strong IT skills, including excellent knowledge of various software programs and packages including MS Word, Excel, and Access.
Prior experience: Minimum of two years of related professional experience.
Skills:
- Ability to multi-task and meet established deadlines.
- Ability to work effectively both as part of a project team and independently.
- Excellent oral and written English communication skills.
- Proven experience using data management systems, tools, and processes to support multi-site, multimode research studies.
- Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to required guidelines, SOPs, and client expectations.
- Good organizational and analytical/problem-solving skills with strong attention to detail.
- Ability to work productively with minimal supervision.
- Ability to attain, maintain, and apply a working knowledge of GCPs and applicable SOPs.
- Strong customer focus and excellent interpersonal skills.
To qualify, applicants must be legally authorized to work in the United States and should not require now, or in the future, sponsorship for employment visa status.
Minimum SalaryUSD $70,000.00/Yr.
Maximum SalaryUSD $70,000.00/Yr.
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Clinical research project manager
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Clinical research project manager
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Senior clinical research associate, cape town based
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