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Our Healthcare client in Johannesburg, South Africa, is seeking two Junior Clinical Researchers to join their team. As a Junior Clinical Researcher, you will be responsible for assisting in the design, implementation, and monitoring of clinical trials and research studies. The role will assist in designing, implementing, and monitoring clinical trials and research studies. Work under the supervision of senior researchers and medical professionals. Ensure research activities adhere to ethical standards, regulatory requirements, and protocol guidelines. The successful candidate will gain valuable experience in clinical research and contribute to medical science advancement.
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•Collaborate with senior researchers to create clinical trial protocols, defining participant eligibility criteria and other relevant aspects.
•Conduct follow-up assessments with participants.
•Monitor adverse events promptly and report them to regulatory bodies and study sponsors.
•Coordinate activities at study sites, from initiation visits to close-out tasks.
•Ensure compliance with protocol requirements and maintain accurate documentation.
•Engage in data analysis, including statistical analysis and interpretation of study results.
•Assist in screening potential participants for eligibility criteria.
•Actively contribute to recruitment efforts.
•Identify and mitigate risks associated with clinical research activities.
•Implement quality assurance measures within the research team.
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•Bachelor’s degree in a relevant scientific field (e.g., Biology, Life Sciences, Nursing, Pharmacy, or related discipline).
•Good Clinical Practice (GCP) certification.
•Minimum of 2 years of relevant experience in clinical research or a related field (preferred).
•Prior experience in assisting with clinical trials, data collection, and regulatory compliance.
•Familiarity with Electronic Data Collection Systems (e.g., OpenClinica, REDCap, or Clindex).
•Competence in statistical software (e.g., SAS, SPSS, or R).
•Understanding of Clinical Trial Management Systems.
•Database handling skills.
•Awareness of regulatory compliance tools.
•Familiarity with data visualization tools.
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•Attractive salary with performance-based bonuses.
•Extensive health and dental insurance coverage.
•Flexible working hours with options for remote work.
•Ample vacation days and paid time off.
•Opportunities for professional development and ongoing education support
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We are an equal opportunity employer and value diversity at our company. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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If you require reasonable adjustments during the application process, please contact our HR department at
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Starting in this role provides invaluable hands-on experience in various aspects of clinical trials and research studies. As they gain proficiency through training and working closely with Senior Clinical Researchers in tasks such as study design, data collection, and regulatory compliance, Junior Clinical Researchers can gain more skills by taking on greater responsibility for monitoring and coordinating clinical trials.
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Submit your application by the due date, July 31st, through the company’s official job application URL as shown on the job application page.
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