13 Chief Medical Officer jobs in South Africa
Senior Specialist: Clinical Risk Management Support
Posted today
Job Viewed
Job Description
What will you do?
To form a component of the GEMS: clinical risk management/ fund management support structure. Conduct research and draft documentation and spearhead internal projects related to the work of the clinical risk or fund management teams. Support the Advanced Specialist: Strategic Sourcing with the development of the strategic sourcing strategy through the identification of cost drivers
drivers including gathering of relevant data from various sources.
- Provide effective and valuable input and guidance to the scheme to support the management of clinical risk
- Oversee the specific SPN relationship together with the fund manager and or senior/advanced clinical risk specialist
- The requirement is to ensure that all SPN operations concerns and requirements are communicated to the Fund managers for awareness and assist with actioning where required with internal role-players
- Perform the majority of medicines-related action items and tactical responses arising from the Scheme meetings
- Preparation of slides for various meetings to address medicines related agenda items and strategic inputs
- Presentation of slides at meetings and fielding of questions
- Handling of Scheme queries and tactical responses as they relate to all medicines matters, including but not limited to: Vaccination, MEL and MPL impact analyses, stock-outs and their impact, trend anomalies and expert panels
- Co-ordination and secretariat for Expert Panels
- Development of Medicine proposals
- Development of Medical Device proposals
- Ad-hoc analyses to support proposals
- Ad-hoc medicine requests
- Ad-hoc appliances request
- Participate in various strategic projects
Qualification and Experience:
- Qualified Pharmacist or Clinical Qualification
- 6 - 8 years' experience in managed care, claims, clinical coding and data analysis
- Knowledge of legislation, industry, PMB, NHI
Knowledge and Skills:
- Knowledge and application of relevant legislation
- Knowledge and application of processes and procedures
- Product and scheme rule knowledge
Turnaround Time
The shortlisting process will only start once the application due date has been reached. The time taken to complete this process will depend on how far you progress and the availability of line managers.
Our Commitment to Transformation
AfroCentric is committed to transformation and embracing diversity. Our Employment Equity plan and targets will be considered as part of the recruitment process. This commitment is what drives us to achieve a diverse workplace with employment equity as a key goal to create an inclusive workforce, representative of the demographics of our society as well as people with disabilities.
Should you not hear from us within a month of applying, consider your application unsuccessful.
Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Clinical Data Management Lead, FSP, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
**Data Team Lead, home-based**
**You'll be responsible for managing end-to-end delivery of data management services for multi-service projects, ensuring quality deliverables on time and within budget. You will direct the team in areas of project planning, execution, financial management, communications and milestone deliverables.**
**Main responsibilities**
**Provide leadership and vision to the team**
**Manage and deliver several large scale, high** **complexity/non-standard** **aspect studies across a range of sponsors and Therapeutic areas**
**Manage sponsors at both Study and Programme Level**
**Manage delivery of areas requiring specific expertise (e.g Process, Finance)**
**Ensure milestones meet timelines and quality deliverables**
**Provide project management expertise working with customer data managers, key decision makers and internal team members to manage continuous process improvements and provide technical expertise**
**Ensure open communications with customer and Quintiles management to manage and meet contractual obligations**
**Provide input for and perform direct negotiations with customer**
**Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders**
**Support DM service delivery with comprehensive DM process and technical expertise in executing projects**
**Create and/or review and sign-off on all data management plan (DMP) documents**
**Track service performance and provide leadership to identify root causes of issues and implement remedial actions**
**Serve as the escalation point for unresolved data issues; work with client data managers, vendors, internal team members for resolution**
**Maintain internal tracking databases and systems**
**Minimum Education & Experience**
**Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field**
**Around 5 years direct Data Management experience, including 3 or more years as a Clinical Data Management project lead is preferred**
**Ability to maintain strong customer relationships**
**Connect to great opportunity**
**#LI-HS1**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Clinical Data Management Lead, FSP, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
**Data Team Lead, home-based**
**You'll be responsible for managing end-to-end delivery of data management services for multi-service projects, ensuring quality deliverables on time and within budget. You will direct the team in areas of project planning, execution, financial management, communications and milestone deliverables.**
**Main responsibilities**
**Provide leadership and vision to the team**
**Manage and deliver several large scale, high** **complexity/non-standard** **aspect studies across a range of sponsors and Therapeutic areas**
**Manage sponsors at both Study and Programme Level**
**Manage delivery of areas requiring specific expertise (e.g Process, Finance)**
**Ensure milestones meet timelines and quality deliverables**
**Provide project management expertise working with customer data managers, key decision makers and internal team members to manage continuous process improvements and provide technical expertise**
**Ensure open communications with customer and Quintiles management to manage and meet contractual obligations**
**Provide input for and perform direct negotiations with customer**
**Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders**
**Support DM service delivery with comprehensive DM process and technical expertise in executing projects**
**Create and/or review and sign-off on all data management plan (DMP) documents**
**Track service performance and provide leadership to identify root causes of issues and implement remedial actions**
**Serve as the escalation point for unresolved data issues; work with client data managers, vendors, internal team members for resolution**
**Maintain internal tracking databases and systems**
**Minimum Education & Experience**
**Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field**
**Around 5 years direct Data Management experience, including 3 or more years as a Clinical Data Management project lead is preferred**
**Ability to maintain strong customer relationships**
**Connect to great opportunity**
**#LI-HS1**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Clinical Data Management Lead, FSP, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
**Data Team Lead, home-based**
**You'll be responsible for managing end-to-end delivery of data management services for multi-service projects, ensuring quality deliverables on time and within budget. You will direct the team in areas of project planning, execution, financial management, communications and milestone deliverables.**
**Main responsibilities**
**Provide leadership and vision to the team**
**Manage and deliver several large scale, high** **complexity/non-standard** **aspect studies across a range of sponsors and Therapeutic areas**
**Manage sponsors at both Study and Programme Level**
**Manage delivery of areas requiring specific expertise (e.g Process, Finance)**
**Ensure milestones meet timelines and quality deliverables**
**Provide project management expertise working with customer data managers, key decision makers and internal team members to manage continuous process improvements and provide technical expertise**
**Ensure open communications with customer and Quintiles management to manage and meet contractual obligations**
**Provide input for and perform direct negotiations with customer**
**Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders**
**Support DM service delivery with comprehensive DM process and technical expertise in executing projects**
**Create and/or review and sign-off on all data management plan (DMP) documents**
**Track service performance and provide leadership to identify root causes of issues and implement remedial actions**
**Serve as the escalation point for unresolved data issues; work with client data managers, vendors, internal team members for resolution**
**Maintain internal tracking databases and systems**
**Minimum Education & Experience**
**Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field**
**Around 5 years direct Data Management experience, including 3 or more years as a Clinical Data Management project lead is preferred**
**Ability to maintain strong customer relationships**
**Connect to great opportunity**
**#LI-HS1**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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Medical Officer
Posted 4 days ago
Job Viewed
Job Description
Take work load off oncologists, creating capacity. Patient care.
Routine follow-ups; Chemotherapy follow-ups; Radiotherapy treatment checks; Emergencies ; Unscheduled patients; Ward rounds; After hours call; Special investigations; Administration; Meetings; Academic presentation; CPD points; Staff medicals if required
Interpersonal Factor
- As a professional all services delivered needs to be in line with the Cancercare Values, of CARE. Each task needs to be consistently executed whilst at all times displaying a positive influence on all stakeholders and within the general working environment. It is expected from the employee to deliver all the tasks reflecting a willingness to operate outside the scope of the job description as per operational requirements. The factors below cannot therefore be reviewed and assessed in isolation.
- To display the company values: C - Compassion, A - Accountability, R - Respect, E - Ethics (CARE)
Routine follow-ups
- History, Examination, Assessment, Plan of action (Profdoc)
- Prescription
- SD/NAD > relevant tests, F/U
- PD > refer to oncologist for treatmet decision
Chemotherapy follow-ups
- History, Examination, Assessment, Plan of action (Profdoc)
- Prescription
- Treatment in chemoroom or treatment delay, cessation
Radiotherapy treatment checks
- History, Examination, Assessment, Plan of action (Profdoc)
- Prescription
- Treatment on Linac or treatment delay, cessation
Emergencies
- Immediate examination and resuscitation
- Possible referral for admission
- Ambulance
- Immediate resuscitation
Unscheduled patients
- History, Examination, Assessment, Plan of action (Profdoc)
- Admission > Tests
- Tests > Prescription
- Appropriate treatment
Ward rounds
- History, Examination, Assessment, Plan of action (Profdoc)
- Prescription in ward
- Treatment in ward (supportive/palliative/optimising for treatment)
After hours call
- Answer after hour call
- Arrange admission
- See emergencies at casualty or in the ward
- Appropriate treatment
Special investigations
- Check and sign all results send to oncologist (per request)
- Inform oncologist of abnormal results
- Treatment decision made
- Follow-up appointment made
Administration
- Life insurance forms
- Medical boarding forms
- Hospice referrals
- Specialist referrals
- Letters to referring doctors
- Oxygen orders
- Blood slips
- Scan and x-ray requests
- Phone calls
- Patient satisfaction
- Increase referrals
- Improve communication
- Readily available information
Meetings
- Different departments communicate
- Dates given through
- Improve workflow
- Improve interrelations
Academic presentations
- 30 min presentation per year
- Improve knowledge
CPD points
- Attend CPD functions to acquire sufficient points per year
- Have 30 CPD points at any given time in a rolling 12 month cycle, 5 of which must be ethics
Required minimum education:
MBChB or equivalent
Required minimum experience:
3 years work experience
Required minimum work-related experience:
To be evaluated on an individual basis
Cancercare, is an equal opportunity employer committed to achieving transformation and embraces diversity and creating an inclusive working environment where all employees are encouraged to reach their full potential, and individual differences are valued and respected. All applicants shall be considered for employment without regard to race, ethnicity, religion, gender, sexual orientation, gender identity, age, and disability status. By submitting your application, you are giving The Cancercare implicit consent to the storage and processing of your personal information
Locum Medical Officer
Posted today
Job Viewed
Job Description
LOCUM MEDICAL OFFICER
Mitchell's Plain Transitional Care Facility (MPTCF) - Managed by Aquarius Health Care NPC/NPO.
Mitchell's Plain Intermediate Care Facility is situated on the premises of Lentegeur Psychiatric Hospital. The facility has 148 beds, responsible for the rehabilitation of patients, wound care, palliative and convalescent care.
KEY RESPONSIBILITIES
- Clinical Assessment of Patients
- Patient assessment should comprise of: Appropriate history and clinical examination, Appropriate investigations in certain circumstances
- Ensure that there are detailed notes in medical records including proper documentation and discharge summaries.
- Ensure that patient rounds have taken place in each ward once per week
- Closely liaise with all referring Hospital Medical Officer/Consultants
- Demonstrate procedures when required.
- Conduct In service training sessions when needed.
- Medication prescribing and re-boarding.
- Death Certification.
- Telephonic on call
- The applicant will work with the multi disciplinary team
MINIMUM REQUIREMENTS
- Minimum of 3 years proven work experience in Palliative/Wound Care and Rehabilitation of patients.
- Registered with HPCSA.
- Excellent organizational and multitasking abilities
- A team player with leadership skills, Excellent communication, and organizational skills.
ADDITIONAL TASK
In addition to the above tasks, the official has to perform any other task (s) not mentioned above as long as it is within his/her capabilities and scope of work.
ADDITIONAL INFORMATION
Please forward 2-3-page CV together with a letter of motivation to: No telephonic enquiries or manual submission of CVS, ONLY on e-mail.
Only shortlisted candidates will be contacted. Locum contract from the13 October 2025 to 31 October 2025.
Applicants, who do not receive a response on their application within 5 working days of the closing date of the advertisement, are to accede that the application was not successful.
AHC NPC reserves the right to defer or close this vacancy at any time.
Applicants, who do not receive a response on their application within 5 working days of the closing date of the advertisement, are to accept that the application was unsuccessful.
AHC reserves the right to defer or close this vacancy at any time.
Job Type: Full-time
Work Location: In person
Research Medical Officer
Posted today
Job Viewed
Job Description
Seeking clinical trial investigator to provide comprehensive medical care/clinical support to participants enrolled into clinical trials at TREAD Research.
Start date : 1 November 2025
1-2 years clinical trial experience is a requirement
Open to work half-day = 7am - 1pm
Key Performance areas:
- Provision of clinical care to patients and participants
- Accurate and comprehensive medical record keeping
- Clinical trial oversight or management as designated by the principal investigator
- Participation in all phases/components of the research process
- Facilitation and resolution of queries from Data Management and Internal/ External Monitors within required timeframe
- Quality Check of Source Documents during participant visit ensuring any outstanding components are proactively addressed
Required minimum education and training:
- Medical Degree (MBCHB)Qualified as Medical Doctor
- Professional body registration: Registered with the Health Professions Council of South Africa
- Excellent clinical skills and attention to detail
- Ability to work under pressure and work well across multiple different projects and teams
- Empathy and sensitivity toward people from key populations
Job Types: Full-time, Part-time
Expected hours: 42.5 per week
Work Location: In person
Expected Start Date: 2025/11/01