Job Description

Locations

• South Africa, Centurion

Skills Required

• medical writing within the biopharmaceuticalintermediate
• clinicalintermediate
• global regulatory requirementsintermediate
• Microsoft Wordintermediate
• electronic document management systemsintermediate
• document templatesintermediate

Required Qualifications

• Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred (degree in a scientific)
• Minimum of 5+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered (experience, 5 years)
• Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development (experience)
• Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements (experience)
• Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams (experience)
• Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information (experience)
• Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines (experience)
• Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed (experience)
• High attention to detail with a commitment to quality, consistency, and scientific accuracy (experience)
• Proficiency in Microsoft Word and document formatting best practices (experience)
• Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools (experience)
• Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred (degree in a scientific)
• Minimum of 5+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered (experience, 5 years)
• Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development (experience)
• Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements (experience)
• Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams (experience)
• Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information (experience)
• Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines (experience)
• Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed (experience)
• High attention to detail with a commitment to quality, consistency, and scientific accuracy (experience)
• Proficiency in Microsoft Word and document formatting best practices (experience)
• Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools (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 https://jobs.iqvia.com (experience)
• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. (experience)

Responsibilities

• Lead the development of high-quality clinical and regulatory documents (e.g., Investigator’s Brochures, Clinical Study Reports, clinical summaries, and marketing authorization submissions) in compliance with global regulatory guidelines (ICH, FDA, EMA) and internal standards
• Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs
• Provide strategic guidance to cross-functional teams on document content, messaging, and regulatory positioning to ensure alignment with program goals
• Manage medical writing projects, including planning, timelines, resource coordination, and delivery to ensure milestones and submission deadlines are met
• Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety, etc.) to gather, interpret, and accurately present clinical data
• Mentor and support other medical writers, ensuring high-quality, scientifically sound, and consistent deliverables across projects
• Review and edit project-related documents to ensure accuracy, clarity, consistency, and compliance with templates and style guides
• Attend project and team meetings to provide expert input on document development, study data interpretation, and process improvements
• Contribute to and lead process improvement initiatives to enhance efficiency, quality, and consistency in document preparation
• Develop, maintain, and refine standard operating procedures (SOPs), templates, and best practices for medical writing
• Stay current with evolving global regulatory requirements, industry trends, and therapeutic area knowledge to ensure compliance and innovation
• Lead the development of high-quality clinical and regulatory documents (e.g., Investigator’s Brochures, Clinical Study Reports, clinical summaries, and marketing authorization submissions) in compliance with global regulatory guidelines (ICH, FDA, EMA) and internal standards
• Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs
• Provide strategic guidance to cross-functional teams on document content, messaging, and regulatory positioning to ensure alignment with program goals
• Manage medical writing projects, including planning, timelines, resource coordination, and delivery to ensure milestones and submission deadlines are met
• Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety, etc.) to gather, interpret, and accurately present clinical data
• Mentor and support other medical writers, ensuring high-quality, scientifically sound, and consistent deliverables across projects
• Review and edit project-related documents to ensure accuracy, clarity, consistency, and compliance with templates and style guides
• Attend project and team meetings to provide expert input on document development, study data interpretation, and process improvements
• Contribute to and lead process improvement initiatives to enhance efficiency, quality, and consistency in document preparation
• Develop, maintain, and refine standard operating procedures (SOPs), templates, and best practices for medical writing
• Stay current with evolving global regulatory requirements, industry trends, and therapeutic area knowledge to ensure compliance and innovation

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