Medical Research jobs in Gauteng
Clinical Data Reviewer
Often replies in 1 dayPSI CROPretoria, Gauteng- You will join a global yet closely-knit team with a shared commitment to developing smart and effective approaches to project monitoring.
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- Discovery Ltd.Sandton, Gauteng
- At least 3 years’ experience in the medical scheme / managed care industry.
- Experience in developing protocols, desk research, clinical policy, benefit designs.
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- Servest CareersSandton, Gauteng
- Data analysis and research skills.
- Check and book medical fitness for personnel.
- The OHS Training Officer will be responsible for ensuring that employees are…
- IQVIACenturion, Gauteng
- Bachelor’s degree in a Health or Science discipline with experience in clinical research.
- Experience working in highly diverse teams within clinical research;…
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- Indisense TechnologyJohannesburg, Gauteng
- Proven experience in the medical field and medical device sales.
- Experience training healthcare professionals on medical devices.
- Experience using a CRM system.
- Dow JonesJohannesburg, Gauteng
- The Research Analyst II, Global Thermal Coal position requires a junior research analyst with a minimum of 2 years of experience in researching coal, iron ore,…
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Clinical Data Reviewer
Often replies in 1 dayPSI CROPretoria, Gauteng- You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data.
- Hybrid position after trial period.
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- Dis-Chem Pharmacies LimitedMidrand, Gauteng
- Competency in quantitative and qualitative research methodology — designing, deploying, and analysing surveys and feedback instruments.
- IQVIACenturion, Gauteng
- Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs.
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- News CorpJohannesburg, Gauteng
- The Research Analyst II, Global Thermal Coal position requires a junior research analyst with a minimum of 2 years of experience in researching coal, iron ore,…
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- United Nations Development Programme (UNDP)Johannesburg, Gauteng
- Policy formulation, research, and advocacy, with previous experience working on comprehensive abortion care an advantage.
- Ampath LaboratoriesCenturion, Gauteng
- You will bring at least three years of experience within a clinical trials environment, coupled with exposure to project management activities within clinical…
- Ampath LaboratoriesCenturion, Gauteng
- You will bring at least three years of experience within a clinical trials environment, coupled with exposure to project management activities within clinical…
- IQVIACenturion, Gauteng
- Work appropriately with internal and external stakeholders to keep up to date with developments in government/regulatory provisions for both commercial and…
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- WildernessJohannesburg, Gauteng
- Escalate medical, legal or reputationally sensitive matters to the Head of Risk promptly.
- Conduct research into regional compliance requirements, regulatory…
- Momentum HealthSandton, Gauteng
- Collaborate with stakeholders in conducting underwriting and medical research in targeted areas, facilitating informed decisionmaking.
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Job Post Details
Job details
Job type
- Full-time
Location
Full job description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description
You will join a global yet closely-knit team with a shared commitment to developing smart and effective approaches to project monitoring. You will have the opportunity to help shape the future of risk-based monitoring at PSI and contribute to ensuring high-quality study data. As part of your role, you will remotely monitor study data, identify potential errors and trends, and flag issues related to site performance.
Hybrid position after trial period.
You will:
- Review EDC, IxRS, Laboratory and other vendors’ data and clinical listings
- Identify single errors and systematic issues related to site performance
- Generate, follow up and resolves data queries and site issues
- Identify and record protocol deviations
- Assist to Central Monitoring Manager with administrative activities, including managing study data, documents and reports
- Ensure site monitors receive information on site related risk & issues. Escalate findings to study teams
- Assists with root cause investigation and follow up on site performance signals identified during central monitoring review
Qualifications
- College/University degree or an equivalent combination of education, training & experience
- Prior experience in Clinical Research
- Experience in central monitoring and clinical data review is a plus
- Full working proficiency in English
- Proficiency in MS Office applications
- Analytical mindset and attention to detail
- Ability to learn, plan and work in a dynamic team environment
Additional Information
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.