37 Fieldwork jobs in South Africa

Overview

Are you an experienced professional in the field of Clinical Research who is deeply passionate about contributing to the South African community and committed to making a meaningful impact and taking on a leadership role? Become part of an organisation dedicated to driving social change and take responsibility for a research site in East London, conducting clinical trials and various projects focused on community engagement, skill development, and alignment with health priorities. The clinical research site leader is responsible for providing administrative and operational oversight for the implementation of multiple clinical trials at the site. Key responsibilities include site management, stakeholder collaboration, staff supervision, meeting study deliverables, reporting, maintaining standard operating procedures (SOPs), and supporting team development.

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Overview

Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes.

Key Responsibilities Project Management

• Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements.
• Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out.
• Monitor study progress and ensure all performance targets are met.
• Prepare progress reports for funders and stakeholders.
• Collaborate with Principal Investigators to resolve internal and external monitoring findings.
• Ensure accurate maintenance of essential documents and Investigator Site Files.
• Attend community and stakeholder meetings to present study updates.
• Contribute to the development and review of SOPs.

Site Management

• Ensure daily operational readiness of the site and clinic facility.
• Allocate staff effectively across multiple studies.
• Conduct regular performance and capacity evaluations.
• Initiate recruitment processes when additional staffing resources are required.
• Act as the primary contact for sponsors and stakeholders.
• Support feasibility assessments by providing accurate site data and capabilities.

Staff Training & Mentorship

• Supervise and mentor research staff.
• Conduct training and retraining based on quality assessments and audit feedback.
• Guide staff in development of publications, abstracts, and presentations.
• Promote ongoing professional development.

Research Outputs

• Lead or contribute to scientific publications and dissemination activities.
• Lead or support the writing of grant proposals.

Qualifications & Registrations

• Master’s Degree in Biomedical/Health or related field (Essential)
• Management Qualification (Essential)
• HPCSA Registration, if applicable
• PhD in a Biomedical/Health related field (advantageous)
• Project Management Certificate
• GCP Certification (Advantageous)

Experience

• Minimum 5 years’ clinical trial management (Essential)
• Minimum 3 years’ clinical research site leadership (Essential)
• Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.)
• Experience with study documentation (protocols, CRFs, SOPs)
• Proven track record in publications and grant writing

Additional Requirements

• Proficiency in English (Essential); Xhosa (Advantageous)
• Proficiency in Microsoft Office
• Ability to utilise Artificial Intelligence (AI) to improve operations
• Willingness to work flexible hours, including weekends as required
• Valid Driver’s License (Essential)

Application Process

How to Apply: To apply, please send your CV and any supporting documents to with the subject line "Clinical”

Closing Date: 12 October 2025 at 16h00

#J-18808-Ljbffr

Overview

Job Title: Clinical Research Site Leader

Department: Research Department

Reports to: Head of Research

Location: Ndevana, Buffalo City Metropolitan Municipality in the Eastern Cape

Annual Salary Range: R737 796 – R1 009 077 (Depending on experience)

Purpose of the Role

Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes.

Responsibilities

• Project Management
  • Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements.
  • Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out.
  • Monitor study progress and ensure all performance targets are met.
  • Prepare progress reports for funders and stakeholders.
  • Collaborate with Principal Investigators to resolve internal and external monitoring findings.
  • Ensure accurate maintenance of essential documents and Investigator Site Files.
  • Attend community and stakeholder meetings to present study updates.
  • Contribute to the development and review of SOPs.
• Site Management
  • Ensure daily operational readiness of the site and clinic facility.
  • Allocate staff effectively across multiple studies.
  • Conduct regular performance and capacity evaluations.
  • Initiate recruitment processes when additional staffing resources are required.
  • Act as the primary contact for sponsors and stakeholders.
  • Support feasibility assessments by providing accurate site data and capabilities.
• Staff Training & Mentorship
  • Supervise and mentor research staff.
  • Conduct training and retraining based on quality assessments and audit feedback.
  • Guide staff in development of publications, abstracts, and presentations.
  • Promote ongoing professional development.
• Research Outputs
  • Lead or contribute to scientific publications and dissemination activities.
  • Lead or support the writing of grant proposals.

Qualifications & Registrations

• Master’s Degree in Biomedical/Health or related field (Essential)
• Management Qualification (Essential)
• HPCSA Registration, if applicable
• PhD in a Biomedical/Health related field (advantageous)
• Project Management Certificate
• GCP Certification (Advantageous)

Experience

• Minimum 5 years’ clinical trial management (Essential)
• Minimum 3 years’ clinical research site leadership (Essential)
• Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.)
• Experience with study documentation (protocols, CRFs, SOPs)
• Proven track record in publications and grant writing

Additional Requirements

• Proficiency in English (Essential); Xhosa (Advantageous)
• Proficiency in Microsoft Office
• Ability to utilise Artificial Intelligence (AI) to improve operations
• Willingness to work flexible hours, including weekends as required
• Valid Driver’s License (Essential)

Application Process

How to Apply: To apply, please send your CV and any supporting documents to with the subject line "Clinical”

Closing Date

12 October 2025 at 16h00

#J-18808-Ljbffr

Job Title: Clinical Research Site Leader

Department: Research Department

Reports to: Head of Research

Location: Ndevana, Buffalo City Metropolitan Municipality in the Eastern Cape

Annual Salary Range: R737 796 – R1 009 077 (Depending on experience)

Purpose of the Role

Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes.

Key Responsibilities:

1. Project Management

• Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements.
• Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out.
• Monitor study progress and ensure all performance targets are met.
• Prepare progress reports for funders and stakeholders.
• Collaborate with Principal Investigators to resolve internal and external monitoring findings.
• Ensure accurate maintenance of essential documents and Investigator Site Files.
• Attend community and stakeholder meetings to present study updates.
• Contribute to the development and review of SOPs.

1. Site Management

• Ensure daily operational readiness of the site and clinic facility.
• Allocate staff effectively across multiple studies.
• Conduct regular performance and capacity evaluations.
• Initiate recruitment processes when additional staffing resources are required.
• Act as the primary contact for sponsors and stakeholders.
• Support feasibility assessments by providing accurate site data and capabilities.

1. Staff Training & Mentorship

• Supervise and mentor research staff.
• Conduct training and retraining based on quality assessments and audit feedback.
• Guide staff in development of publications, abstracts, and presentations.
• Promote ongoing professional development.

1. Research Outputs

• Lead or contribute to scientific publications and dissemination activities.
• Lead or support the writing of grant proposals.

Qualifications & Registrations:

• Master’s Degree in Biomedical/Health or related field (Essential)
• Management Qualification (Essential)
• HPCSA Registration, if applicable
• PhD in a Biomedical/Health related field (advantageous).
• Project Management Certificate
• GCP Certification (Advantageous)

Experience:

• Minimum 5 years’ clinical trial management (Essential)
• Minimum 3 years’ clinical research site leadership (Essential)
• Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.)
• Experience with study documentation (protocols, CRFs, SOPs)
• Proven track record in publications and grant writing

Additional Requirements:

• Proficiency in English (Essential); Xhosa (Advantageous)
• Proficiency in Microsoft Office
• Ability to utilise Artificial Intelligence (AI) to improve operations
• Willingness to work flexible hours, including weekends as required
• Valid Driver’s License (Essential)

Application Process:

Job Title: Clinical Research Site Leader

Department: Research Department

Reports to: Head of Research

Location: Ndevana, Buffalo City Metropolitan Municipality in the Eastern Cape

Annual Salary Range: R737 796 – R1 009 077 (Depending on experience)

Purpose of the Role

Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes.

Key Responsibilities:

1. Project Management

• Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements.
• Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out.
• Monitor study progress and ensure all performance targets are met.
• Prepare progress reports for funders and stakeholders.
• Collaborate with Principal Investigators to resolve internal and external monitoring findings.
• Ensure accurate maintenance of essential documents and Investigator Site Files.
• Attend community and stakeholder meetings to present study updates.
• Contribute to the development and review of SOPs.

1. Site Management

• Ensure daily operational readiness of the site and clinic facility.
• Allocate staff effectively across multiple studies.
• Conduct regular performance and capacity evaluations.
• Initiate recruitment processes when additional staffing resources are required.
• Act as the primary contact for sponsors and stakeholders.
• Support feasibility assessments by providing accurate site data and capabilities.

1. Staff Training & Mentorship

• Supervise and mentor research staff.
• Conduct training and retraining based on quality assessments and audit feedback.
• Guide staff in development of publications, abstracts, and presentations.
• Promote ongoing professional development.

1. Research Outputs

• Lead or contribute to scientific publications and dissemination activities.
• Lead or support the writing of grant proposals.

Qualifications & Registrations:

• Master’s Degree in Biomedical/Health or related field (Essential)
• Management Qualification (Essential)
• HPCSA Registration, if applicable
• PhD in a Biomedical/Health related field (advantageous).
• Project Management Certificate
• GCP Certification (Advantageous)

Experience:

• Minimum 5 years’ clinical trial management (Essential)
• Minimum 3 years’ clinical research site leadership (Essential)
• Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.)
• Experience with study documentation (protocols, CRFs, SOPs)
• Proven track record in publications and grant writing

Additional Requirements:

• Proficiency in English (Essential); Xhosa (Advantageous)
• Proficiency in Microsoft Office
• Ability to utilise Artificial Intelligence (AI) to improve operations
• Willingness to work flexible hours, including weekends as required
• Valid Driver’s License (Essential)

Application Process:

The clinical research site leader is responsible for providing administrative and operational oversight for the implementation of multiple clinical trials at the site. Key responsibilities include site management, stakeholder collaboration, staff supervision, meeting study deliverables, reporting, maintaining standard operating procedures (SOPs), and supporting team development.

KEY SUMMARY OF POSITION:

(For the sake of brevity and easy reading, only a key summary of the full job specification / job advert as provided by the client is provided below. Additional information and full details regarding the position and potential employer will be provided following our initial contact and the CV review)

PROJECT MANAGEMENT

• Lead and oversee multiple clinical studies, ensuring adherence to GCP, protocols, SOPs, and sponsor/internal standards; standardize study processes across planning, activation, recruitment, data management, and closeout phases.
• Monitor study performance, address findings from monitoring reports with PIs, maintain essential documents, provide stakeholder updates, engage with communities, and contribute to SOP development.

SITE MANAGEMENT

• Oversee daily clinic operations, including staff allocation across studies, performance evaluation, and prompt recruitment to ensure optimal site performance and resource availability.
• Act as the main point of contact for sponsors and stakeholders, and support study feasibility assessments by providing insights on site capabilities, patient demographics, and logistics.

STAFF TRAINING & MENTORSHIP

• Supervise, mentor, and support site staff to uphold high research standards, including training based on quality and monitoring feedback.
• Promote professional development by guiding staff in scientific writing, presentations, and ongoing skill enhancement.

RESEARCH OUTPUTS

• Lead and contribute to scientific publications and research dissemination.
• Lead or significantly contribute to writing of grant proposals
  

QUALIFICATIONS AND REGISTRATION

• Masters Degree in a Biomedical/Health related field (essential).
• Current registration with the Health Professions Council of South Africa, if applicable.
• Management qualification (essential).
• PhD in a Biomedical/Health related field (advantageous).
• Project Management qualification (advantageous).
• Valid GCP certification (advantageous).

EXPERIENCE

• Minimum of 5 years experience managing clinical trials (essential).
• Minimum of 3 years demonstrated experience in clinical research site management and leading site research teams (essential).
• Comprehensive understanding of the current regulatory requirements pertaining to clinical trials (essential).
• Experience with regulatory submissions to SAHPRA, Ethics Committees, and other regulatory authorities (essential).
• Study trial document development including protocols, case report forms, and SOPS.
• Contribution to scientific publications and grant proposals.Minimum of 5 years experience managing clinical trials (essential).
• Minimum of 3 years demonstrated experience in clinical research site management and leading site research teams (essential).
• Comprehensive understanding of the current regulatory requirements pertaining to clinical trials (essential).
• Experience with regulatory submissions to SAHPRA, Ethics Committees, and other regulatory authorities (essential).
• Study trial document development including protocols, case report forms, and SOPS.
• Contribution to scientific publications and grant proposals.

OTHER REQUIREMENTS

• Proficiency in reading, speaking, and writing English.
• Proficiency in reading, speaking, and writing Xhosa (advantageous).
• Proficiency in Microsoft Office.
• Embracing and leveraging Artificial Intelligence (AI), to enhance operational efficiency.
• Willingness to work reasonable flexible hours, including weekends, if required, in accordance with the BCEA.
• Valid drivers license (essential).

SALARY:

This role is open to candidates at varying levels, and the final remuneration package will be tailored to reflect your individual qualifications, skills, and experience.

Job Title: Clinical Research Site Leader Department: Research Department Reports to: Head of Research Location: Ndevana, Buffalo City Metropolitan Municipality in the Eastern Cape Annual Salary Range: R737 796 – R1 009 077 (Depending on experience) Purpose of the Role Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes. Key Responsibilities: Project Management Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements. Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out. Monitor study progress and ensure all performance targets are met. Prepare progress reports for funders and stakeholders. Collaborate with Principal Investigators to resolve internal and external monitoring findings. Ensure accurate maintenance of essential documents and Investigator Site Files. Attend community and stakeholder meetings to present study updates. Contribute to the development and review of SOPs. Site Management Ensure daily operational readiness of the site and clinic facility. Allocate staff effectively across multiple studies. Conduct regular performance and capacity evaluations. Initiate recruitment processes when additional staffing resources are required. Act as the primary contact for sponsors and stakeholders. Support feasibility assessments by providing accurate site data and capabilities. Staff Training & Mentorship Supervise and mentor research staff. Conduct training and retraining based on quality assessments and audit feedback. Guide staff in development of publications, abstracts, and presentations. Promote ongoing professional development. Research Outputs Lead or contribute to scientific publications and dissemination activities. Lead or support the writing of grant proposals. Qualifications & Registrations: Master’s Degree in Biomedical/Health or related field (Essential) Management Qualification (Essential) HPCSA Registration, if applicable PhD in a Biomedical/Health related field (advantageous). Project Management Certificate GCP Certification (Advantageous) Experience: Minimum 5 years’ clinical trial management (Essential) Minimum 3 years’ clinical research site leadership (Essential) Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.) Experience with study documentation (protocols, CRFs, SOPs) Proven track record in publications and grant writing Additional Requirements: Proficiency in English (Essential); Xhosa (Advantageous) Proficiency in Microsoft Office Ability to utilise Artificial Intelligence (AI) to improve operations Willingness to work flexible hours, including weekends as required Valid Driver’s License (Essential) Application Process:

The clinical research site leader is responsible for providing administrative and operational oversight for the implementation of multiple clinical trials at the site. Key responsibilities include site management, stakeholder collaboration, staff supervision, meeting study deliverables, reporting, maintaining standard operating procedures (SOPs), and supporting team development. KEY SUMMARY OF POSITION: (For the sake of brevity and easy reading, only a key summary of the full job specification / job advert as provided by the client is provided below. Additional information and full details regarding the position and potential employer will be provided following our initial contact and the CV review) PROJECT MANAGEMENT Lead and oversee multiple clinical studies, ensuring adherence to GCP, protocols, SOPs, and sponsor/internal standards; standardize study processes across planning, activation, recruitment, data management, and closeout phases. Monitor study performance, address findings from monitoring reports with PIs, maintain essential documents, provide stakeholder updates, engage with communities, and contribute to SOP development. SITE MANAGEMENT Oversee daily clinic operations, including staff allocation across studies, performance evaluation, and prompt recruitment to ensure optimal site performance and resource availability. Act as the main point of contact for sponsors and stakeholders, and support study feasibility assessments by providing insights on site capabilities, patient demographics, and logistics. STAFF TRAINING & MENTORSHIP Supervise, mentor, and support site staff to uphold high research standards, including training based on quality and monitoring feedback. Promote professional development by guiding staff in scientific writing, presentations, and ongoing skill enhancement. RESEARCH OUTPUTS Lead and contribute to scientific publications and research dissemination. Lead or significantly contribute to writing of grant proposals QUALIFICATIONS AND REGISTRATION Masters Degree in a Biomedical/Health related field (essential). Current registration with the Health Professions Council of South Africa, if applicable. Management qualification (essential). PhD in a Biomedical/Health related field (advantageous). Project Management qualification (advantageous). Valid GCP certification (advantageous). EXPERIENCE Minimum of 5 years experience managing clinical trials (essential). Minimum of 3 years demonstrated experience in clinical research site management and leading site research teams (essential). Comprehensive understanding of the current regulatory requirements pertaining to clinical trials (essential). Experience with regulatory submissions to SAHPRA, Ethics Committees, and other regulatory authorities (essential). Study trial document development including protocols, case report forms, and SOPS. Contribution to scientific publications and grant proposals.Minimum of 5 years experience managing clinical trials (essential). Minimum of 3 years demonstrated experience in clinical research site management and leading site research teams (essential). Comprehensive understanding of the current regulatory requirements pertaining to clinical trials (essential). Experience with regulatory submissions to SAHPRA, Ethics Committees, and other regulatory authorities (essential). Study trial document development including protocols, case report forms, and SOPS. Contribution to scientific publications and grant proposals. OTHER REQUIREMENTS Proficiency in reading, speaking, and writing English. Proficiency in reading, speaking, and writing Xhosa (advantageous). Proficiency in Microsoft Office. Embracing and leveraging Artificial Intelligence (AI), to enhance operational efficiency. Willingness to work reasonable flexible hours, including weekends, if required, in accordance with the BCEA. Valid drivers license (essential). SALARY: This role is open to candidates at varying levels, and the final remuneration package will be tailored to reflect your individual qualifications, skills, and experience.

Job Title: Clinical Research Site Leader Department: Research Department Reports to: Head of Research Location: Ndevana, Buffalo City Metropolitan Municipality in the Eastern Cape Annual Salary Range: R737 796 – R1 009 077 (Depending on experience) Purpose of the Role Together with our client, we are recruiting for a Clinical Research Site Leader based in Zintenteni, Ndevana in the Eastern Cape. The Site Leader will provide administrative and operational leadership in the implementation of multiple clinical trials at the site. This role is accountable for site management, stakeholder coordination, staff supervision, reporting, SOP compliance, and team development, ensuring the successful delivery of all study outcomes. Key Responsibilities: Project Management Oversee and implement multiple studies according to timelines, ensuring compliance with GCP, study protocols, SOPs and sponsor requirements. Standardise processes for planning, activation, recruitment, enrolment, data cleaning and study close-out. Monitor study progress and ensure all performance targets are met. Prepare progress reports for funders and stakeholders. Collaborate with Principal Investigators to resolve internal and external monitoring findings. Ensure accurate maintenance of essential documents and Investigator Site Files. Attend community and stakeholder meetings to present study updates. Contribute to the development and review of SOPs. Site Management Ensure daily operational readiness of the site and clinic facility. Allocate staff effectively across multiple studies. Conduct regular performance and capacity evaluations. Initiate recruitment processes when additional staffing resources are required. Act as the primary contact for sponsors and stakeholders. Support feasibility assessments by providing accurate site data and capabilities. Staff Training & Mentorship Supervise and mentor research staff. Conduct training and retraining based on quality assessments and audit feedback. Guide staff in development of publications, abstracts, and presentations. Promote ongoing professional development. Research Outputs Lead or contribute to scientific publications and dissemination activities. Lead or support the writing of grant proposals. Qualifications & Registrations: Master’s Degree in Biomedical/Health or related field (Essential) Management Qualification (Essential) HPCSA Registration, if applicable PhD in a Biomedical/Health related field (advantageous). Project Management Certificate GCP Certification (Advantageous) Experience: Minimum 5 years’ clinical trial management (Essential) Minimum 3 years’ clinical research site leadership (Essential) Strong understanding of South African regulatory requirements (SAHPRA, Ethics submissions, etc.) Experience with study documentation (protocols, CRFs, SOPs) Proven track record in publications and grant writing Additional Requirements: Proficiency in English (Essential); Xhosa (Advantageous) Proficiency in Microsoft Office Ability to utilise Artificial Intelligence (AI) to improve operations Willingness to work flexible hours, including weekends as required Valid Driver’s License (Essential) Application Process: