25 Medical Specialist jobs in South Africa
MEDICAL SPECIALIST - RADIATION ONCOLOGY
Posted 5 days ago
Job Viewed
Job Description
- Package : R1 341 855.00 per annum (all-inclusive remuneration package)
Requirements :
- Appropriate qualification that allows registration with the HPCSA as a Medical specialist in Radiation Oncology. Registration with the HPCSA as a Medical Specialist in Radiation Oncology. No experience required after registration with the HPCSA as Medical Specialist in Radiation Oncology.
Duties :
- The successful candidate will be expected to render full spectrum of Radiation Oncology services at the department of radiation Oncology. Attends multi-disciplinary meetings. Conducts clinical assessment and formulation of treatments plans for patients. Plans and deliver Radiotherapy treatments, assessments and follow-ups. Assists with patient backlogs in treatment and ensure effective delivery of radiation therapy in a safe, evidence based, ethical way considering health economics. Assist the Head of Department with the day-to-day management of the unit. Oversee the work of Registrars to ensure adequate service delivery. Assist with the teaching program in the department of Radiation Oncology, including attendance and participation in academic meetings, providing supervision, informal and formal teaching to Registrars. The successful candidate will be involved in clinical research as well as supervising registrars on their MMeds. The employee will be required to work longer hours the assessment and treatment of Radiation Oncology emergencies.
Notes :
- Kindly note that NO payment of any kind is required when applying for posts advertised by the Gauteng Department of Health.The Department reserves the right not to fill any advertised posts.Applications should be submitted strictly online at the following E-Recruitment portal: No hand-delivered, faxed, or emailed applications will be accepted. For assistance with online applications please email your query to Applications should be accompanied by a fully completed and signed new Z83 form obtainable from any Public Service Department or on the internet at The new Z83 form must be fully completed and signed by the applicant. The following must be considered in relation to the completion of the Z83 by applicants: All the fields in Part A, Part C and Part D must be completed. Leave the following question blank if they are not in possession of such: “If your profession or occupation requires official registration, provide date and particulars of registration”. Application without proof of a new Z83 application form and detailed CV will be disqualified. Applicants must indicate the post reference number on their applications. Shortlisted candidates will receive communication from HR unit to submit certified copies of educational qualifications and other relevant documents not older than 6 months on or before the day of the interview). Personnel Suitability Checks (criminal checks, citizenship checks, qualification verification, company directorship, social media, financial record checks, reference checks) must be conducted prior appointment. Candidates in possession of a foreign qualification must furnish the Department with an evaluation certificate from the South African Qualifications Authority (SAQA). Applicants with foreign qualifications remain responsible for ensuring that their qualifications are evaluated by the South African Qualifications Authority (SAQA). Registrars will be required to rotate between the different institutions. Preference will be given to South African citizens. The performance of normal and commuted overtime is not mandatory, however it will be based on the operational needs of the hospitals.
Employer : Department of Health
Closing Date : 25-07-2025
Criteria Questions
Do you have an appropriate qualification that allows registration with the HPCSA as a Medical specialist in Radiation Oncology?
Do you have a registration with the HPCSA as a Medical Specialist in Radiation Oncology?
Please Notes :
- Due to the large number of applications we envisage receiving, applications will not be acknowledged. If youdo not receive any response within 3 months, please accept that your application was not successful.
Medical Content Specialist
Posted 7 days ago
Job Viewed
Job Description
Medical Content Specialist - South Africa
About the job
Inizio Medical is growing! We are expanding our team of Medical Content Specialists based in the South Africa. Our South Africa team will work alongside our global teams in ApotheCom, Nucleus Global and Ashfield MedComms across the US, UK, EU, and Philippines which will give you the opportunity to work on cutting edge projects, working at the forefront of drug development and commercialization.
Combining complex scientific understanding with creativity, Inizio Medical develops impactful medical affairs strategies and compelling communications. Underpinned by world-class medical analytics capabilities and applied AI tools, Inizio Medical redefines the role of medical affairs in drug development and commercialization.
Principal Role :
You are responsible for (a) accuracy checks of scientific content drafted by medical writers and / or clients, (b) managing citations eg sourcing and marking up references, uploading to and linking on document review platforms, (c) generating data tables and simple figures, (d) collating medical journal metrics from online database, (e) extracting data from scientific papers for consideration in systematic literature reviews, (f) checking alignment of manuscript content to standard reporting guidelines, (g) performing program landscaping for key international conferences.
Academic Background :
- A medical degree
- An advanced degree in a biomedical subject
- Nursing or pharmacist qualification
Skills Required :
Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.
#J-18808-LjbffrMedical Sales Specialist Midrand
Posted 9 days ago
Job Viewed
Job Description
Leading medical supplier is looking for a Sales and Application Specialist to join their team. A Radiography / Sonography qualification is required.
Duties & ResponsibilitiesMinimum Requirements:
Grade 12 certificate as a minimum requirement.
Radiography / Sonography qualification and working experience is required.
Previous sales experience would be an advantage.
Own transport is essential.
Duties:
- Developing an in-depth knowledge of the Ultrasound product range and services provided.
- Responsible for the sales of the ultrasound products, including maintaining and growing existing business and expanding sales within the assigned territory.
- Scheduling and attending appointments with existing and potential customers.
- Demonstration of products to Clinical personnel and on-going training and support to customers.
- Completion of weekly planner and activity report for submission to direct manager.
- Achieving Sales Targets.
- Responsible for networking with and development of relationships with new customers and managing existing customers.
- Correct Management of demo stock.
- Preparing and following up on quotations.
- Attending meetings, conferences and exhibitions as required promoting Ultrasound products and services.
- Analysing the market and providing business feedback by using all available support tools.
- General Administration associated with the position.
Monthly plus Basic salary, car allowance, medical aid, provident fund.
#J-18808-LjbffrMedical Researcher Deputy Director (Specialist Medical Doctor)
Posted 4 days ago
Job Viewed
Job Description
Our well-established client in the pharmaceutical industry has a vacancy available for a Medical Researcher Deputy Director (Specialist Medical Doctor) to be based at the Parktown office.
Main Purpose of Job
To lead the design, execution, and oversight of all clinical research and development programs within the company. The Medical Research Deputy Director will apply medical and scientific expertise to drive innovation, oversee clinical trial design and execution, ensure regulatory compliance, and support the development of safe and effective pharmaceutical products aligned with the organization’s strategic objectives.
To oversee the Medical Affairs in the company.
Key Performance Areas (Core, essential responsibilities –outputs of the position)
Area Description
Clinical Trial Leadership - Lead the design and execution of Phase I–IV clinical trials, ensuring scientific and ethical integrity.
- Review and approve study protocols, investigator brochures, and clinical development plans.
Medical Oversight - Provide clinical guidance on drug development projects.
- Serve as the medical expert in cross-functional project teams.
Regulatory Compliance - Ensure adherence to GCP (Good Clinical Practice), ICH guidelines, SAHPRA regulations.
- Support the preparation of clinical sections of regulatory submissions and responses to authorities.
Scientific Innovation - Guide research strategy and medical innovation aligned with therapeutic focus areas.
- Evaluate opportunities for new molecules, reformulations, indications.
Team Collaboration - Collaborate with the team of researchers, medical writers, and clinical operations staff.
- Foster a high-performance and learning-oriented environment.
Stakeholder Engagement - Liaise with Key Opinion Leaders (KOLs), investigators, and academic institutions.
- Represent the company at scientific conferences and advisory boards.
Data Review & Analyse and interpret clinical data for decision-making.
Interpretation publications and presentations
- Ensure data integrity, safety reporting, and ethical standards.
Cross-Functional - Work closely with Regulatory Affairs, Pharmacovigilance, Medical
Integration - Affairs, and Marketing to align research with commercial and regulatory
goals
Minimum Requirements
EDUCATION
- MBChB/ Medical Doctor with Speciality Qualifications
EXPERIENCE.
- Experience in clinical research and execution of clinical trials
- Experience in the pharmaceutical industry will be an added
advantage
- Prior experience of using AI in research is highly advantageous
SKILLS/PHYSICAL COMPETENCIES
- Strategic thinking and high attention to detail.
- Leadership, collaboration, and cross-functional communication.
- High ethical standards and commitment to patient safety.
General working conditions (e.g. shift work, driver’s license, specific tools, special clothing, environmental requirements, etc.)
- Office-based most with business travel where and when required.
- Flexibility to work outside of regular office hours, as needed, to accommodate business
- requirements.
- Own driver’s license and transport.
Please attach cv, qualifications, id and drivers license
#J-18808-Ljbffr
Medical Researcher Deputy Director (Specialist Medical Doctor)
Posted today
Job Viewed
Job Description
Our well-established client in the pharmaceutical industry has a vacancy available for a Medical Researcher Deputy Director (Specialist Medical Doctor) to be based at the Parktown office. Main Purpose of Job
To lead the design, execution, and oversight of all clinical research and development programs within the company. The Medical Research Deputy Director will apply medical and scientific expertise to drive innovation, oversee clinical trial design and execution, ensure regulatory compliance, and support the development of safe and effective pharmaceutical products aligned with the organization’s strategic objectives. To oversee the Medical Affairs in the company. Key Performance Areas (Core, essential responsibilities –outputs of the position)
Area Description Clinical Trial Leadership - Lead the design and execution of Phase I–IV clinical trials, ensuring scientific and ethical integrity.
- Review and approve study protocols, investigator brochures, and clinical development plans. Medical Oversight - Provide clinical guidance on drug development projects.
- Serve as the medical expert in cross-functional project teams. Regulatory Compliance - Ensure adherence to GCP (Good Clinical Practice), ICH guidelines, SAHPRA regulations.
- Support the preparation of clinical sections of regulatory submissions and responses to authorities. Scientific Innovation - Guide research strategy and medical innovation aligned with therapeutic focus areas.
- Evaluate opportunities for new molecules, reformulations, indications. Team Collaboration - Collaborate with the team of researchers, medical writers, and clinical operations staff.
- Foster a high-performance and learning-oriented environment. Stakeholder Engagement - Liaise with Key Opinion Leaders (KOLs), investigators, and academic institutions.
- Represent the company at scientific conferences and advisory boards. Data Review & Analyse and interpret clinical data for decision-making.
Interpretation publications and presentations
- Ensure data integrity, safety reporting, and ethical standards. Cross-Functional - Work closely with Regulatory Affairs, Pharmacovigilance, Medical
Integration - Affairs, and Marketing to align research with commercial and regulatory
goals Minimum Requirements
EDUCATION
- MBChB/ Medical Doctor with Speciality Qualifications EXPERIENCE.
- Experience in clinical research and execution of clinical trials
- Experience in the pharmaceutical industry will be an added
advantage
- Prior experience of using AI in research is highly advantageous SKILLS/PHYSICAL COMPETENCIES
- Strategic thinking and high attention to detail.
- Leadership, collaboration, and cross-functional communication.
- High ethical standards and commitment to patient safety. General working conditions (e.g. shift work, driver’s license, specific tools, special clothing, environmental requirements, etc.) - Office-based most with business travel where and when required.
- Flexibility to work outside of regular office hours, as needed, to accommodate business
- requirements.
- Own driver’s license and transport. Please attach cv, qualifications, id and drivers license #J-18808-Ljbffr
Medical Researcher Deputy Director (Specialist Medical Doctor)_Jhb
Posted today
Job Viewed
Job Description
Medical Researcher Deputy Director (Specialist Medical Doctor)
Business Unit : Medical Research Department
Geographic Location
Parktown, Johannesburg
Number of Immediate Subordinates / Direct Reports x 1
Main Purpose of Job
To lead the design, execution, and oversight of all clinical research and development programs within the company. The Medical Research Deputy Director will apply medical and scientific expertise to drive innovation, oversee clinical trial design and execution, ensure regulatory compliance, and support the development of safe and effective pharmaceutical products aligned with the organization’s strategic objectives.
To oversee the Medical Affairs in the company.
Key Performance Areas (Core, essential responsibilities –outputs of the position)
Area
Description
Clinical Trial Leadership
- Lead the design and execution of Phase I–IV clinical trials, ensuring scientific and ethical integrity.
- Review and approve study protocols, investigator brochures, and clinical development plans.
Medical Oversight
- Provide clinical guidance on drug development projects.
- Serve as the medical expert in cross-functional project teams.
Regulatory Compliance
- Ensure adherence to GCP (Good Clinical Practice), ICH guidelines, SAHPRA regulations.
- Support the preparation of clinical sections of regulatory submissions and responses to authorities.
Scientific Innovation
- Guide research strategy and medical innovation aligned with therapeutic focus areas.
- Evaluate opportunities for new molecules, reformulations, indications.
- Collaborate with the team of researchers, medical writers, and clinical operations staff.
- Foster a high-performance and learning-oriented environment.
Stakeholder Engagement
- Liaise with Key Opinion Leaders (KOLs), investigators, and academic institutions.
- Represent the company at scientific conferences and advisory boards.
Data Review & - Analyze and interpret clinical data for decision-making,
Interpretation publications and presentations
- Ensure data integrity, safety reporting, and ethical standards.
Cross-Functional - Work closely with Regulatory Affairs, Pharmacovigilance, Medical
Integration - Affairs, and Marketing to align research with commercial and regulatory
goals
EDUCATION
- MBChB / Medical Doctor with Specialty Qualifications
EXPERIENCE .
- Experience in clinical research and execution of clinical trails
- Experience in the pharmaceutical industry will be an added
advantage
- Prior experience of using AI in research highly advantageous
SKILLS / PHYSICAL COMPETENCIES
- Strategic thinking and high attention to detail.
- Leadership, collaboration, and cross-functional communication.
- High ethical standards and commitment to patient safety.
General working conditions (e.g. shift work, drivers’ license, specific tools, special clothing, environmental requirements, etc.)
- Office based most with business travel where and when required.
- Flexibility to work outside of regular office hours, as needed, to accommodate business
- requirements.
- Own driver’s license and transport.
Medical Medical • Johannesburg, South Africa
#J-18808-LjbffrMedical Researcher Deputy Director (Specialist Medical Doctor)_JHB
Posted 9 days ago
Job Viewed
Job Description
Job Title
Medical Researcher Deputy Director (Specialist Medical Doctor)
Business Unit: Medical Research Department
Geographic Location
Parktown, Johannesburg
Number of Immediate Subordinates/ Direct Reports x 1
Main Purpose of Job
To lead the design, execution, and oversight of all clinical research and development programs within the company. The Medical Research Deputy Director will apply medical and scientific expertise to drive innovation, oversee clinical trial design and execution, ensure regulatory compliance, and support the development of safe and effective pharmaceutical products aligned with the organization’s strategic objectives.
To oversee the Medical Affairs in the company.
Key Performance Areas (Core, essential responsibilities –outputs of the position)
Area
Description
Clinical Trial Leadership
- Lead the design and execution of Phase I–IV clinical trials, ensuring scientific and ethical integrity.
- Review and approve study protocols, investigator brochures, and clinical development plans.
Medical Oversight
- Provide clinical guidance on drug development projects.
- Serve as the medical expert in cross-functional project teams.
Regulatory Compliance
- Ensure adherence to GCP (Good Clinical Practice), ICH guidelines, SAHPRA regulations.
- Support the preparation of clinical sections of regulatory submissions and responses to authorities.
Scientific Innovation
- Guide research strategy and medical innovation aligned with therapeutic focus areas.
- Evaluate opportunities for new molecules, reformulations, indications.
Team Collaboration
- Collaborate with the team of researchers, medical writers, and clinical operations staff.
- Foster a high-performance and learning-oriented environment.
Stakeholder Engagement
- Liaise with Key Opinion Leaders (KOLs), investigators, and academic institutions.
- Represent the company at scientific conferences and advisory boards.
Data Review & - Analyze and interpret clinical data for decision-making,
Interpretation publications and presentations
- Ensure data integrity, safety reporting, and ethical standards.
Cross-Functional - Work closely with Regulatory Affairs, Pharmacovigilance, Medical
Integration - Affairs, and Marketing to align research with commercial and regulatory
goals
Minimum Requirements
EDUCATION
- MBChB/ Medical Doctor with Specialty Qualifications
EXPERIENCE .
- Experience in clinical research and execution of clinical trails
- Experience in the pharmaceutical industry will be an added
advantage
- Prior experience of using AI in research highly advantageous
SKILLS/PHYSICAL COMPETENCIES
- Strategic thinking and high attention to detail.
- Leadership, collaboration, and cross-functional communication.
- High ethical standards and commitment to patient safety.
General working conditions (e.g. shift work, drivers’ license, specific tools, special clothing, environmental requirements, etc.)
- Office based most with business travel where and when required.
- Flexibility to work outside of regular office hours, as needed, to accommodate business
- requirements.
- Own driver’s license and transport.
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Medical Equipment Theatre Specialist (Roaming) - N
Posted 9 days ago
Job Viewed
Job Description
Reference: PTA022464-MB-1
Salary package: R18 000 - 23 000 Basic + Fleet Card + Laptop + Cellphone allowance
Clinical Representative (NEURO) - Medical Company
- BSc in Anatomy / Physiology / or Human Sciences with 4+ years experience in Theatre (Hospitals) / Neuro, Brain / Spine
- MUST be able to follow Hospital and Doctor's protocol
- Very reliable with a strong but balanced personality; very presentable
- Must be able to work late should there be a procedure in the hospital
- Ability to think on feet
- Roaming Clinic Representative / Equipment handling
- Travel to assist in theatre at State and Private Hospitals
- Fluent in Afrikaans & English
- Valid driver's license / Own reliable vehicle
- Must be extremely presentable and professional
- Excellent interaction and communication skills
Consultant: Marelize Bester - Dante Personnel Pretoria Silver Lakes
Apply via our website you do not hear from us within 5 days, please accept that your application was unsuccessful.
Medical Sales and Application Specialist
Posted 9 days ago
Job Viewed
Job Description
Leading medical supplier is looking for a Sales and Application Specialist to join their team. A Radiography / Sonography qualification is required.
Duties & ResponsibilitiesMinimum Requirements:
Grade 12 certificate as a minimum requirement
Radiography / Sonography qualification and working experience is required
Own transport is essential
Previous sales experience would be an advantage.
- Developing an in-depth knowledge of the Ultrasound product range and services provided
- Responsible for the sales of the ultrasound products, including maintaining and growing existing business and expanding of sales within the assigned territory
- Scheduling and attending appointments with existing and potential customers
- Demonstration of products to Clinical personnel and on-going training and support to customers
- Completion of weekly planner and activity report for submission to direct manager
- Achieving Sales Targets
- Responsible for networking with and development of relationships with new customers and managing existing customers
- Correct Management of demo stock
- Preparing and following up on quotations
- Attending meetings, conferences and exhibitions as required promoting Ultrasound products and services
- Analysing the market and providing business feedback by using all available support tools
- General Administration associated with the position
Monthly plus Basic salary, car allowance, medical aid, provident fund.
#J-18808-LjbffrProduct Specialist- (Medical Equipment- ICU & Theatre) R40K - R50K CTC
Posted 9 days ago
Job Viewed
Job Description
Calling all product specialists within the Medical sectors. Positions available in Vaal region, Westrand, and Jhb.
The Product Specialist/Trainer is responsible for supporting sales in all product trainings nationally on all product groups: Anesthesia, Monitoring, Ventilation, and WPI.
The Product Trainer will provide support to account managers when needed after demonstrations and installations. They will work as a team with the account managers to increase customer support and optimal use of products.
Candidate must have worked and have experience in Theatre and ICU, therefore understanding medical terms.
Duties & ResponsibilitiesThe Product Specialist/Trainer is responsible for supporting sales in all product trainings nationally on all product groups: Anesthesia, Monitoring, Ventilation, and WPI.
The Product Trainer will provide support to account managers when needed after demonstrations and installations. They will work as a team with the account managers to increase customer support and optimal use of products.
Desired Experience & Qualification- ICU and/or Theatre postgraduate or equivalent diploma/certificate
- Minimum 3 years working experience in the field of ICU and Theatre equipment