Senior Medical Writer – Maternity Cover

🔥 13 hours ago

🇬🇧 United Kingdom – Remote

⏳ Contract/Temporary

🟠 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.

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Bionical Emas

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1998

🏥 Healthcare

📦 Logistics

💊 Pharmaceuticals

Healthcare • Logistics • Pharmaceuticals

Bionical Emas is a B2B life sciences services company that provides clinical development and pharmaceutical support, including clinical trial supply, regulatory affairs, pharmacovigilance, medical affairs, quality assurance, and distribution/logistics. The company appears to support pharmaceutical and biotech organizations with trial management, patient access, and related operational services, and recruits professionals across these functions.

📋 Description

• Lead and manage medical writing activities across the company • Research, create, and edit documents associated with Early Access Programmes, including Real-World Data (RWD) • Create patient consent and assent forms, patient information sheets, Early Access Program protocols, RWD protocols, lay summary reports, investigator brochures and updates, clinical study manuscripts, and clinical study reports • Serve as the primary client contact for content development • Understand client expectations and meet them through teamwork, deadline adherence, scientific knowledge, and content development • Collaborate with internal operational teams to ensure content is accurate and tailored to client needs • Participate in internal and external meetings to discuss content and deliverable status • Monitor assigned projects and manage own workload • Anticipate capacity issues and provide potential solutions • Delegate deliverables to medical writer vendors when required • Manage medical writer vendors, including budgets and invoices • Facilitate process improvement to ensure deliverables are high quality, accurate, and meet client needs

🎯 Requirements

• Prior medical writing experience in clinical research/pharmaceutical industry/medical communications • Experience working directly with clients/sponsors • Experience preparing document timelines • Experience organizing review cycles • Experience coordinating review meetings • Bachelor’s degree in a Healthcare/Science related subject • Demonstrated understanding of early access programs, clinical research, the drug development process, and applicable regulatory guidelines and regulations • Function as a team-player, highly organised, self-motivated, and extremely detail-oriented • Strong oral and written communication skills • Excellent interpersonal skills • Advanced computer literacy of MS Office Suite • Ability to write at a level appropriate to the target audience • Effective time management skills and ability to manage competing priorities • Ability to work in a cross-functional environment • Understanding of the integration of AI-enabled solutions to streamline documentation and reduce QC timelines

🏖️ Benefits

• 25 days of vacation • Vacation days purchasing scheme • 1 extra vacation day per each 3 years of service • Discretionary Annual Bonus • Sabbatical of 3 to 6 months (after 2 years of service) • Free food and beverages at all offices • Life Insurance • Health Insurance and Employee Assistance Programme • Employee Support Networks • Flexible and hybrid work • Welcoming, flexible, and supportive culture • Personal development opportunities