Job Status: Full Time 

Date: 26th July 2024 

Content Writer – Pharmacovigilance

At Rxlogix.com, we’re at the forefront of pharmacovigilance solutions, committed to enhancing patient safety and regulatory compliance for life sciences companies. We’re seeking a seasoned Content Writer to join our team and amplify our brand, marketing, and sales initiatives.

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.