Medical Writer, Disclosure

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

💵 $96.2k - $151.4k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥📝 Medical Writer

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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MSD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1891

🏥 Healthcare

📦 Logistics

🧬 Biotechnology

Healthcare • Logistics • Biotechnology

MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.

📋 Description

• Prepare medical and clinical disclosure writing deliverables • Apply principles of clinical research, clinical trial design, and statistics to interpret data • Manage multiple projects in deadline-driven environments • Work independently and collaboratively with cross-functional teams • Interact with stakeholders through oral, written, and presentation-based communication • Author or support clinical regulatory documents, protocol registrations/results disclosures, medical publications, or regulatory product labeling

🎯 Requirements

• Bachelor’s degree preferably in a health, scientific, or relevant discipline (e.g., life sciences, pharmacy, medicine, public health) • At least 2 years of relevant industry experience • Knowledge of clinical research principles, clinical trial design, and fundamental statistics • Strong attention to detail, analytical/logical thinking, critical evaluation and interpretation of data, and problem-solving capabilities • Ability to manage multiple projects in a deadline-driven environment, independently and collaboratively within cross-functional teams • Strong oral and written communication, interpersonal, and presentation skills • Technical expertise in Microsoft Office Suite and shared document systems such as SharePoint • Willingness to learn and adapt to emerging technology • Familiarity with United States and/or European Union legislation for clinical trial registration and result disclosure (preferred) • Technical or medical authoring experience with clinical regulatory documents, protocol registrations/results disclosures, medical publications, or regulatory product labeling (preferred)

🏖️ Benefits

• Annual bonus and long-term incentive, if applicable • Medical, dental, vision healthcare and other insurance benefits for employee and family • Retirement benefits, including 401(k) • Paid holidays • Vacation • Compassionate and sick days • Remote work arrangement • No travel required • No relocation