Medical Writer

🔥 18 minutes ago

🇮🇳 India – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Quanticate

WebsiteLinkedInAll Job Openings

201 - 500 employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

Quanticate is a leading global biometric Contract Research Organisation (CRO) specializing in clinical data analysis for the pharma and biotech industries. They provide a range of services focused on enhancing clinical trial efficiency and success, including biostatistics, clinical data management, medical writing, and pharmacovigilance. Quanticate leverages advanced methodologies, such as Bayesian approaches, to optimize trial execution and data standardization, ensuring compliance with regulatory standards. They offer scalable resources tailored to client needs and have expertise across various therapeutic areas and trial phases, from early Phase I to post-marketing Phase IV trials. Quanticate is known for its robust data automation, visualisation, and analytics capabilities, which support decision-making and regulatory submissions.

📋 Description

• 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.

🎯 Requirements

• 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.

🏖️ Benefits

• 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