
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
🔥 0 minutes ago
🌲 North Carolina – Remote
💵 $65k - $129k / year
⏰ Full Time
🟠 Senior
✏️ Content Writer
🦅 H1B Visa Sponsor
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1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
• Develop robust proposals, leading the writing, coordination, and presentation of our responses in Microsoft Word, PowerPoint, and other systems/formats • Work with Account Directors and SMEs to effectively manage the proposal development process • Actively participate in project strategy discussions, ensuring product/service offerings are clearly articulated in proposals • Proofread, edit, rewrite, and revise documents to ensure readability, consistency, accuracy, and relevance • Meet proposal deadlines by establishing priorities and target dates for information gathering, writing, reviews, approvals, and signatures • Act as a focal point to collect information from various sources.
• Minimum two years’ experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate – Writing • Bachelor's degree; master’s or PhD preferred (prefer degree in Life Sciences, Communications, Journalism, or Marketing) • Experience drafting RFIs in a CRO environment, or in pharma/biotech outsourcing preferred • Knowledge of the CRO/pharmaceutical industry • Strong customer relationship management skills and strong commercial acumen.
• Competitive benefits package depending on location • Pay equity and transparency
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