Medical Writer

• Author, review, and quality-check regulatory and scientific documents, including clinical study reports and other medical writing deliverables.
• Ensure documents accurately reflect source data, meet regulatory requirements, and comply with company and client standards.
• Manage document review cycles, resolve reviewer comments, and coordinate feedback from multiple stakeholders.
• Provide editorial support, proofreading, and quality control reviews.
• Support document publishing and compilation of submission-ready deliverables.
• Manage multiple writing projects within agreed timelines and budgets.
• Track project milestones, risks, and progress using project management tools.
• Collaborate with project teams, reviewers, and subject matter experts.
• Maintain project records, including time reporting and tracking metrics.
• Serve as a client point of contact and maintain client relationships.
• Support proposal development, bid defence meetings, and business development activities.
• Contribute to client satisfaction and service improvement initiatives.
• Train, guide, and mentor junior Medical Writers and team members.
• Promote knowledge sharing, best practices, process improvement, and innovation.
• Stay current with regulatory requirements, GCP standards, and scientific communication guidelines.
• Share regulatory updates and industry best practices with colleagues and clients.
• Engage with industry forums and professional networks.

• Master's degree in Life Sciences, Medical Sciences, Pharmacy, or a related scientific discipline.
• A PhD, PharmD, MD, MVSc, or equivalent advanced qualification is desirable.
• 4+ years of medical writing experience within the pharmaceutical, biotechnology, CRO, or healthcare sector.
• Strong experience preparing regulatory and scientific documents.
• Solid understanding of regulatory requirements and scientific communication guidelines.
• Experience mentoring or supporting the development of colleagues.
• Publications in peer-reviewed scientific literature would be advantageous.
• Exceptional written and verbal communication skills.
• Ability to translate complex scientific concepts into clear, concise, and audience-appropriate content.
• Strong attention to detail and commitment to quality.
• Excellent organisational, project management, and prioritisation skills.
• Strong analytical and problem-solving abilities.
• Ability to work independently while contributing effectively within cross-functional teams.
• Confident stakeholder management, influencing, and negotiation skills.
• Proficiency with Microsoft Office and document management systems.
• Commitment to continuous learning and professional development.

• Competitive salary
• Flexible working hours
• Holidays (Annual Leave, Sick Leave, Casual Leave and Bank holidays)
• Medical Insurance for self and immediate family
• Gratuity
• Accidental Coverage
• Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e- learning, job shadowing)
• Membership to professional societies
• Career development opportunities