Technical writer Work, Jobs in Snodland, Ken (with Salaries)

Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Bachelor's degree
- Medical terminology
Quick apply
Technical Author
QinetiQ —Ashford
- Full-time
- CAD
- Microsoft Office
- Mechanical knowledge
- Employee discount
Process Lead
South East Water —Snodland
- £43,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
ASSISTANT BID WRITER
Laing O'Rourke —Dartford
- Organisational skills
- IT
- Communication skills
Proposal Writer - Global Payments Proposal & Solutions Group
JPMorganChase —London
- Full-time
- Microsoft Word
- Microsoft Excel
- Sales
Bid & Content Writer
Regular Cleaning —London
- £28,000 - £30,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Microsoft Office
- Store discount
- Health & wellbeing programme
Quick apply
BEMM Author & Analyst (Project & Process Support)
Select Engineering —Basildon
- £26.82 - £34.83 an hour
- Call to connect
- Microsoft Word
- Project management
- AI
10d
Senior Bid Writer
United Infrastructure —Dartford
- Full-time
- Microsoft Word
- English
- No degree
- Referral programme
Quick apply
1d

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Content Writer - Pharmacovigilance

RxLogix Corporation -
London

Quick apply

Job details

Full-time

Qualifications

Bachelor's degree
Technical writing
Medical terminology

Full job description

Company Overview:

RxLogix is a global leader in pharmacovigilance solutions, providing innovative software and expert consulting services. Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain.

Dedicated to patient safety and the advancement of medical and scientific research, RxLogix values bold, innovative thinkers. We leverage the latest technologies, including machine learning and artificial intelligence, to set new industry standards.

Recently, the FDA selected RxLogix's PV Surveillance Suite Platform to replace its legacy FAERS signaling system, utilizing our modules for advanced data analytics, signal detection, evaluation, signal management, and benefit-risk assessment.

Job Description:

We’re on the hunt for a dynamic, creative Content Writer with a solid background in pharmacovigilance. This role calls for a strategic thinker who can understand our product offerings and create compelling content that resonates with our target audience.

Key Responsibilities:

Content Creation: Develop engaging, informative content for various platforms, including our website, blog, social media, email campaigns, white papers, case studies, and sales collateral. Your content should be SEO-friendly to improve website rankings and drive organic traffic.
Brand Building: Craft content that effectively communicates the value of Rxlogix’s pharmacovigilance products and services, enhancing brand awareness and positioning in the market.
Marketing Support: Collaborate with the marketing team to create content that supports marketing strategies, campaigns, and initiatives specific to pharmacovigilance.
Digital Marketing: Develop content for PPC campaigns, social media ads, and other digital marketing efforts. Manage content for social media platforms to increase engagement, followers, and brand visibility within the pharmacovigilance community.
Sales and Pre-Sales Support: Develop compelling content for sales presentations, product demos, and pre-sales materials to support the sales team in closing deals.
Research and Collaboration: Stay updated on industry trends, competitive landscape, and customer needs to ensure content is relevant and impactful. Work closely with product managers, sales, and marketing teams to understand product features, benefits, and use cases, and translate them into compelling content.

Key Qualifications:

Education: Bachelor’s degree in Pharmacovigilance, Life Sciences, Pharmacy, Medicine, or a related field.
Regulatory and Compliance: Strong understanding of pharmacovigilance principles, drug safety regulations, and industry guidelines. Knowledge of regulatory requirements for drug safety reporting (e.g., FDA, EMA). Adherence to regulatory requirements and industry best practices in all content development activities.
Scientific and Technical Writing: Proficiency in medical terminology and scientific writing. Excellent writing skills with attention to detail and accuracy. Competence in reviewing and editing pharmacovigilance documents.
Research and Data Analysis: Ability to interpret clinical trial data and scientific literature. Skill in conducting literature searches and critically evaluating scientific literature. Familiarity with pharmacovigilance databases and reporting systems.
Content Development and Communication: Experience in pharmaceutical or healthcare communications. Capability to develop educational materials and proficiency in authoring and communicating pharmacovigilance communication strategies.
Collaboration and Teamwork: Ability to collaborate with pharmacovigilance experts, medical writers, regulatory affairs professionals, and other stakeholders. Experience in participating in cross-functional teams to support pharmacovigilance initiatives and projects.

Location: Hybrid, London, UK

Quick apply

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technical writer jobs in snodland, ken

Content Writer - Pharmacovigilance

Technical Author

Process Lead

ASSISTANT BID WRITER

Proposal Writer - Global Payments Proposal & Solutions Group

Bid & Content Writer

BEMM Author & Analyst (Project & Process Support)

Senior Bid Writer

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