54 Medical Lead jobs in South Africa

Do you have expertise in, and passion for science working in Oncology creating value for our customers and patients? If so, AstraZeneca might be the one for you!

ABOUT ASTRAZENECA

AstraZeneca is a global, innovation-driven Biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. Our strategic priorities reflect how we are working to deliver our strategy and achieve our Purpose.As a workforce, we are the catalyst for our values: we are entrepreneurial; we do the right thing; we play to win; we put patients first and we follow the science. As a company we appreciate and take great pride in each team member where every person is brought together through shared values, that underpins a shared purpose. There’s no better place to feel inspired and energised.

At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. Join the fastest-growing pharmaceutical in our markets, set up to fuel further growth. Be part of our shared ambition and pride: our strong heritage, our turnaround story, and early investment and commitment in international markets. There’s no better place to feel inspired and energized.

About the Medical Affairs team

You will be joining a high-performing medical team recognized for combining deep medical expertise with strategic insight in a fast-paced, dynamic environment. Our team thrives on problem-solving and embraces an agile, enterprise mindset, always ready to take initiative and adapt to new challenges. We proactively take accountability, continuously push beyond our comfort zones, and are committed to delivering exceptional results for patients and the organization.

What you will do

Act as a catalyst for change by leveraging a deep understanding of the healthcare system—including its environment, priorities, clinical pathways, and patient journeys—to gather actionable insights and execute medical strategic plans. Your work will drive scalable and sustainable clinical practice transformations, improve patient access to equitable, high-quality care, and facilitate the adoption of innovative medicines.

You will build and strengthen professional relationships with healthcare professionals and key stakeholders in alignment with the Integrated Engagement Plan. By providing credible, up-to-date scientific, technical, and pharmaco-economic information, you will support informed decisions through one-on-one discussions, medically led meetings, and expert activities that inspire confidence. Additionally, you may participate in or lead evidence generation initiatives, contributing to the successful implementation of the broader medical strategy.

Job Description

As a field-based scientific expert in oncology, you will drive the execution of Medical Affairs Plans for both pre-launch and newly launched AstraZeneca products and indications. You will shape clinical practice through scientific engagement, partnerships, and collaboration—not only with traditional experts like specialist KEEs/KOLs, expert, and primary care physicians, but also with non-traditional stakeholders such as policy makers, patient advocacy groups, government representatives, and innovative solution providers. Working closely with internal teams, you will champion improved patient outcomes and the safe, effective use of AstraZeneca medicines by building bridges across the healthcare ecosystem.

You will develop and enhance professional partnerships with healthcare professionals and key external stakeholders in alignment with the Integrated Engagement Plan. By providing scientific, technical, and pharmaco-economic information through one-on-one dialogues, medical meetings, and confidence-building activities, you will position yourself as a trusted source of expertise. You will also contribute to—or lead—evidence generation activities that support and implement the broader medical strategy.

Typical Accountabilities

Scientific Expertise :

• Maintain clinical/scientific expertise in disease state management, AstraZeneca products, emerging therapies, and the competitive landscape.

• Contribute to the development and provide project leadership/ management of the therapeutic area Field Medical Strategic Plan (FMSP).

• Act as a subject matter expert/resource for internal and external stakeholders.

• Work with internal stakeholders in the development and delivery of appropriate training and mentoring needs within therapeutic area.

Scientific Exchange:

• Engage in peer-to-peer level dialogue with key customers and deliver appropriate clinical/scientific content through utilising the correct channel mix, which will differentiate AstraZeneca products from those of other companies.

• Respond to unsolicited customer inquiries and provide focused and balanced clinical / scientific information that supports the safe and appropriate use of AstraZeneca’s products and services.

• Provide scientific/clinical support and deliver presentations to internal and external stakeholders.

• Identify and establish relationships with key customers and other scientific thought leaders for engaging them in ongoing scientific dialogue on AstraZeneca products and unsolicited discussions about compounds in development.

• Organize and facilitate scientific events such as MSL Medical events, Symposiums, Scientific Exchanges, Advisory Boards/Expert Panels, non-promotional standalone events, Meet the Professor sessions, etc., with KEEs and HCPs. Prioritize these events based on their relevance in the patient journey for the related disease.

• Deliver informative lectures at scientific events tailored to healthcare professionals, aligning with the field medical communication strategy.

• Collaborate with KEEs on study proposals (ESR or Local Study) and/or publications of interest to AstraZeneca.

Customer Insights and Strategic Relationships:

• Effectively identify, gather, analyse, synthesise, report and forward relevant new knowledge about the external scientific/medical environments to internal stakeholders

• Provide internal stakeholders with actionable items related to medical / product strategy or clinical development based on customer perspectives.

• Partner with traditional and non-traditional stakeholders to identify gaps in the patient experience journey as insights to be included in the medical / product strategies.

If this sounds appealing, please read on to understand the experience and skills we’re looking for…

ESSENTIAL SKILLS AND EXPERIENCE REQUIRED

• Must be a Qualified Medical Doctor or completed / MSc/PhD in a scientific discipline.

• Must have minimum 3- 5 years in a medical affairs role.

• Proven Medical/Scientific knowledge and experience in the responsible disease area.

• Interest in a long-term career in the pharmaceutical industry.

• MSc/PhD in a scientific discipline would be advantageous.

• Understanding of multiple aspects within Medical Affairs.

• Project management experience.

• Excellent presentation and communication skills.

• Ability to travel.

• Fluency in English is required.

Why AstraZeneca?

AstraZeneca recognized as Top Employer | South Africa, Kenya & Nigeria 2025. Best Place to Work in Ivory Coast, Senegal, Cameroon, Ghana & Ethiopia 2024 – 2025.

Furthermore, we are proud to have achieved the impressive feat of ranking second place in theBest Places to Work for the second consecutive year running in Africa.This distinction is a confirmation of our commitment and ability to sustain people, partnerships, and employee engagement and foster an innovative workplace environment.

At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Join the fastest-growing pharmaceutical in our markets, set up to fuel further growth. Be part of our shared ambition and pride: our strong heritage, our turnaround story, and early investment and commitment in International markets. There’s no better place to feel inspired and energized.

SO, WHAT’S NEXT?

Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you!

Click the link to apply no later than 31 July 2025 and we’ll be in touch as soon as we can.

WHERE CAN I FIND OUT MORE?

Our Social Media, Follow AstraZeneca on LinkedIn

Follow AstraZeneca on Facebook

Close Date: 31/07/2025

Date Posted

24-Jul-2025

Closing Date

31-Jul-2025

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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Make a difference with St John Ambulance and become a lifesaver in your community. Gain new skills, support others, and be the hero your community needs!

Are you committed to delivering high-quality care? Do you have experience working as part of a multidisciplinary team?

Position Overview

As a County Lead of East London, you will be part of the establishment of a County St John Council to oversee and guide volunteer Community Networks. This aims to create a structured and supportive framework that empowers volunteers to operate more effectively and efficiently. By providing strategic leadership, coordination, and oversight, the council ensures that volunteer efforts align with community needs and priorities while avoiding duplication of services.

St John has embarked on a journey to achieve the goal of ensuring that every community and young person across the country is first aid confident.

Key Responsibilities

1. Provide strategic leadership and oversight to volunteer Community Networks.
2. Ensure alignment of volunteer efforts with community needs and priorities.
3. Interact with relevant Communities of Practice to share learning, advice, and best practices.
4. Inspire and support volunteers in your county.

Qualifications

We are looking for a leader with a passion for local volunteering and helping communities.

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Make a difference with St John Ambulance and become a lifesaver in your community. Gain new skills, support others, and be the hero your community needs!

Are you committed to delivering high-quality care? Do you have experience working as part of a multidisciplinary team?

Position Overview

As a County Lead of East London, you will be part of the establishment of a County St John Council to oversee and guide volunteer Community Networks. This aims to create a structured and supportive framework that empowers volunteers to operate more effectively and efficiently. By providing strategic leadership, coordination, and oversight, the council ensures that volunteer efforts align with community needs and priorities while avoiding duplication of services.

St John has embarked on a journey to achieve the goal of ensuring that every community and young person across the country is first aid confident.

Key Responsibilities

1. Provide strategic leadership and oversight to volunteer Community Networks.
2. Ensure alignment of volunteer efforts with community needs and priorities.
3. Interact with relevant Communities of Practice to share learning, advice, and best practices.
4. Inspire and support volunteers in your county.

Qualifications

We are looking for a leader with a passion for local volunteering and helping communities.

#J-18808-Ljbffr

Make a difference with St John Ambulance and become a lifesaver in your community. Gain new skills, support others, and be the hero your community needs! Are you committed to delivering high-quality care? Do you have experience working as part of a multidisciplinary team? Position Overview As a County Lead of East London, you will be part of the establishment of a County St John Council to oversee and guide volunteer Community Networks. This aims to create a structured and supportive framework that empowers volunteers to operate more effectively and efficiently. By providing strategic leadership, coordination, and oversight, the council ensures that volunteer efforts align with community needs and priorities while avoiding duplication of services. St John has embarked on a journey to achieve the goal of ensuring that every community and young person across the country is first aid confident. Key Responsibilities Provide strategic leadership and oversight to volunteer Community Networks. Ensure alignment of volunteer efforts with community needs and priorities. Interact with relevant Communities of Practice to share learning, advice, and best practices. Inspire and support volunteers in your county. Qualifications We are looking for a leader with a passion for local volunteering and helping communities. #J-18808-Ljbffr

• iso 134852016 medical device lead assessor

ISO 13485:2016 Medical Device Lead Assessor

Are you an experienced auditor with a passion for quality in the medical device industry? Join our team as an ISO 13485:2016 Lead Assessor at JC Auditors, a leading conformity assessment body with a client-focused approach to promoting medical device performance and efficacy.

• Employment Type: Freelance Contract
• Industry: Medical Devices | Quality Assurance | Regulatory Compliance
• Experience: Minimum 5 years
• Travel: Extensive

What You'll Do:

• Conduct ISO 13485:2016 audits for medical device manufacturers and suppliers
• Assess compliance with regulatory and quality requirements (SAHPRA)
• Provide expert guidance on risk management, QMS implementation, and continual improvement
• Work with a dynamic team committed to upholding the highest industry standards

What We’re Looking For :

• BSc Degree in one or more health science professional areas (biomedical science, medical science, microbiology, chemistry, biochemistry, bioengineering, human physiology, pharmacy, physics)
• Certified Lead Auditor for ISO 13485:2016 (IRCA registered course preferred)
• Minimum of 5 years work experience in the medical device industry
• Proven experience in auditing medical device organizations and conducting 3 rd party- audits
• Current Audit Log reflecting all completed audits and technical areas
• Strong experience in medical devices, SAHPRA regulatory compliance and quality assurance
• Knowledge of related standards (ISO 14971, ISO 9001) and global regulatory frameworks
• Knowledge of MD5, MD9 and ISO 17021
• Ability to travel
• Excellent communication and stakeholder engagement skills
• Excellent analytical, writing and reporting skills

Why Join Us?

• Work with a globally recognized conformity assessment body
• Opportunity to make an impact in the medical device industry
• Professional growth and continuous learning

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IQVIA Bloemfontein, Free State, South Africa

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Join to apply for the Decentralized Clinical Trial Lead role at IQVIA

IQVIA Bloemfontein, Free State, South Africa

Join to apply for the Decentralized Clinical Trial Lead role at IQVIA

As a DCT Study Lead (remote position), you will be at the forefront of transforming clinical research through decentralized and hybrid trial models. You will lead the strategic planning and operational execution of DCT components across global studies, ensuring seamless integration of digital health technologies, remote services, and patient-centric solutions. This role requires strong leadership, cross-functional collaboration, and a deep understanding of clinical trial delivery in a virtual or hybrid setting.

Key Responsibilities

• Project Leadership & Strategy
• Lead the end-to-end delivery of decentralized and hybrid clinical trials, ensuring alignment with contractual obligations, timelines, and quality standards.
• Orchestrate the project DCT team to drive execution, accountability and continuous alignment across functions.
• Serve as the primary DCT contact for clients, internal teams, and vendors, providing strategic oversight and operational direction.
• Collaborate with traditional study teams to integrate DCT elements into broader trial frameworks.
  
  

• Cross-Functional Collaboration
• Partner with internal stakeholders including technology integrations, mobile nursing, regulatory, site support, and data management to ensure cohesive delivery.
• Drive the development of integrated study management plans and ensure milestone achievement.
  
  

• Risk & Quality Management
• Proactively identify risks and implement mitigation strategies.
• Monitor quality metrics and ensure compliance with GCP, SOPs, and regulatory requirements.
• Apply lessons learned
  
  

• Financial Oversight
• Manage project budgets, resource allocation, and financial forecasting.
• Identify scope changes and lead the change control process, including client negotiations.
  
  

• Client Engagement & Communication
• Lead client meetings, bid defenses, and DCT-specific presentations.
• Act as a trusted advisor to clients, offering insights on DCT strategy, innovation, and best practices.
  
  

• Team Leadership & Development
• Contribute to internal training and knowledge-sharing initiatives on DCT methodologies.
  

Qualifications & Skills

• Bachelor’s degree in Life Sciences or related field.
• Minimum 3 years of experience in clinical research,
• Proven track record in in project management, client engagement, and cross-functional leadership.
• Nice to have: Interest of DCT technologies (e.g., eConsent, telehealth, wearables, remote monitoring).
• Excellent communication, negotiation, and presentation skills.
• Ability to navigate ambiguity rapid adjusting strategies and workflow.
• Proficiency in MS Office and clinical trial systems (CTMS, eTMF, etc.).
• Experience with DCT platform implementation or digital health tools.
• Financial acumen and experience managing project budgets.
• Ability to work across geographies and cultures.
• Strong problem-solving and decision-making capabilities.
• Highly goal-oriented upon client needs and agreements
• Passion for innovation and continuous improvement in clinical trial delivery.
  
  

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

Seniority level

• Seniority level Not Applicable

Employment type

• Employment type Full-time

Job function

• Job function Research, Analyst, and Information Technology
• Industries Pharmaceutical Manufacturing

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Job category: Health, Fitness, Medical and Optometry

Location: Roodepoort

Contract: Permanent

Business Unit: Constantia Kloof

Remuneration: R 1,167,990.00

EE position: No

Introduction

Are you a recently qualified clinical pathologist or haemato-pathologist looking for a career path that includes a focus on public wellbeing, service and research - while being patient-centric?Perhaps a career in the South African National Blood Service is for you?The middle manager in this position will have the potential to grow into a senior manager within the SANBS Medical Division – and may over time even progress to executive level.The incumbent will be responsible for:1. Providing medical oversight, guidance and timely medical advice to all technical laboratories and related areas – including the immuno-hematology and cellular therapy laboratories in SANBS – within his/her area of expertise.2. Providing training and development in the area of expertise to both internal and external stakeholders.3. Planning, implementing and monitoring medical related initiatives in the area of responsibility.4. Providing a medical consulting and support service in the area of expertise to both internal and external stakeholders.

Key Performance Areas:

• Strategic Business Planning & Implementation Relating to Transfusion Medicine
• Quality Assurance and Compliance to Standards of Practice, Policies, Procedures and Protocols
• Improving integral processes in Transfusion Medicine
• Customer /Stakeholder Relationship Building
• Aligned people management
• Conducting Research that leads to innovative implementation of solutions

Cognitive:

• Analytical thinking and Attention to Detail
• Change Management
• Holistic / Big Picture Thinking
• Judgement and Decision
• Innovation thinking
• Problem Solving
• Planning, Organising and Monitoring

Personal:

• Ethical behaviour
• Excellence orientation
• Flexibility / Adaptability
• Personal Development
• Resilience and Stress Management
• Drive and Belief in the Cause
• Self Management
• Professional Image and Visibility

Interpersonal:

• Customer Service Orientation
• Conflict Management
• Knowledge sharing
• Organisational Awareness
• Persuasiveness / Selling skills
• Relationship building
• Teamwork
• Communication

Professional/ Technical:

• Building and living the brand
• Business and Financial Acumen
• Process engineering / System competence
• Technical / Professional Competence:
• Best practice thinking

Leadership:

• Motivating People
• Strategic leadership

Principles of Excellence:

• Transparency
• Respect
• Accountability
• Diversity

Equity Statement:

1. All applications will be considered with reference to SANBS' Employment Equity Plan

2. Please consider your application unsuccessful should you not be contacted within three weeks after the closing date

Furthermore note that no advertisement may in any way make reference to /or exclude anybody based on race, gender etc.

Education:

• MB. Ch.B with a post graduate qualification in either haemato- or clinical pathology or related field that enables the sign out of laboratory results.
• Registered with HPCSA

Experience:

• Demonstrable IT literacy in major business applications

Other (knowledge and skills):

• Experience working in a clinical quality system
• Knowledge of Good Manufacturing Practice, Good Laboratory Practice and accreditation.
• Understanding of clinical indications for the transfusion of blood products would be advantageous.
• Understanding of Haemovigilance practices and procedures would be advantageous.

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RESPONSIBILITIES

• 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

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**RESPONSIBILITIES**
+ 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.
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