Manager, Medical Affairs – Scientific Review

🔥 14 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👔 Manager

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 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

EVERSANA

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

💼 Consulting

🏥 Healthcare

⚕️ Healthcare Insurance

Consulting • Healthcare • Healthcare Insurance

EVERSANA is a comprehensive service provider focused on integrated commercial solutions for the life sciences industry. The company offers a wide range of services including advisory and management consulting, regulatory consulting, patient services, market access strategies, pricing and revenue management, medical affairs, and digital transformation. EVERSANA is known for its expertise in drug commercialization, enabling companies to effectively launch and manage pharmaceutical products. With a platform powered by data and analytics, EVERSANA addresses challenges related to drug pricing, market access, patient adherence, and product delivery, helping companies optimize their commercial strategies and enhance patient outcomes. The company emphasizes innovation and has been recognized for its use of AI and data analytics within the life sciences sector.

📋 Description

• Lead medical and scientific review of promotional and non-promotional materials for assigned products and markets • Serve as scientific reviewer and subject matter expert for assigned therapeutic areas and products • Ensure data are scientifically accurate, contextually correct, editorially accurate, scientifically balanced, and compliant • Evaluate clinical and statistical relevance of claims and data • Ensure claims are adequately supported by data and determine reference acceptability • Advise whether claims are consistent with approved labeling • Ensure materials are relevant and useful for target audiences • Collaborate with Medical Affairs, Legal, Regulatory, Commercial, and cross-functional reviewer and writer teams • Participate in Medical, Legal, and Regulatory review committees • Review and approve country-specific materials for regulatory and client compliance • Contribute to scientific narratives, medical presentations, publications, meeting materials, and medical information content • Maintain expertise in therapeutic areas, industry standards, regulatory requirements, publication practices, and review platforms such as Veeva • Support regulatory submissions of promotional materials and associated documentation when required • Support the Global Medical Information / Medical Content Development Team on client engagements • Establish project plans with project management when applicable • Own client deliverables, including timeliness and quality • Coordinate and participate in client meetings, agendas, action items, and follow-up • Write and develop materials and perform quality assurance of writers' and graphic designers' deliverables • Use EVERSANA and client document management platforms such as Veeva PromoMats and MedComms as content owner • Attend MLR meetings and cross-functional team meetings when appropriate • Demonstrate commitment to diversity, equity, and inclusion • Deliver client delight, manage quality issues, and ensure timely corrective and preventive actions

🎯 Requirements

• Applicants must be legally authorized to work in Europe and hold a valid work permit • Advanced degree in Medicine, Pharmacy, or a related healthcare discipline • Minimum 2 years of experience reviewing promotional and non-promotional materials for scientific accuracy, regulatory compliance, and adherence to industry standards • Fluency in English (written and spoken) is required • Additional European language(s) may be required based on market responsibilities and are a plus • Strong understanding of pharmaceutical regulations, industry codes, and compliance requirements governing promotional and non-promotional communications within Europe • Knowledge of EMA regulations and guidance, the EFPIA Code, the ABPI Code of Practice, and relevant country-specific laws, regulations, and industry codes • Familiarity with requirements governing interactions with healthcare professionals, healthcare organizations, patients, and patient organizations • Strong analytical, critical-thinking, and problem-solving skills • Ability to evaluate scientific literature, clinical data, and promotional claims for medical accuracy and regulatory compliance • Exceptional written, verbal, interpersonal, and presentation skills • Ability to communicate complex scientific information clearly and effectively • Ability to effectively collaborate with cross-functional teams, health authorities, clients, and external stakeholders • Ability to establish credibility with internal and external audiences • Demonstrated project management, organizational, and time-management skills • Ability to manage multiple priorities in a fast-paced environment • High attention to detail and commitment to scientific excellence and compliance • Highest standards of professionalism, integrity, ethical conduct, and sound judgment • Pharm.D., Pharm.M., or Medical Degree strongly preferred • Over 5 years of experience reviewing promotional and non-promotional medical materials preferred • Expertise in developing global Medical Information content, including Scientific Response Documents (SRDs), Frequently Asked Questions (FAQs), and Custom Response Documents (CRDs) preferred • ABPI Final Signatory certification/status or demonstrated capability to complete company-approved Final Signatory training and ABPI assessment • Experience with Veeva Vault PromoMats/MedComms, digital solutions, AI, advanced data analytics, automation, and AI applications preferred

🏖️ Benefits

• Full-time, home-based position • Commitment to continuous professional development and staying current with industry trends and regulatory changes • Great Place to Work certified employer • Diversity, equity, and inclusion-focused workplace • Equal Opportunity Employer