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An innovative firm in the pharmaceutical industry seeks a detail-oriented Regulatory Editor II/Senior Regulatory Editor. This full-time remote position offers the opportunity to work collaboratively with medical writers, ensuring high-quality editorial reviews and adherence to regulatory standards. Candidates will leverage their expertise in MS Word and English grammar while contributing to impactful scientific documentation. Join a team that values creativity and flexibility, where your passion for editing can thrive and make a difference in clinical development.
Join to apply for the Regulatory Editor II/Senior Regulatory Editor role at Acumen Medical Communications.
Since its founding in 2016, Acumen Medical Communications has provided high-quality medical writing and clinical development expertise to clients in the pharmaceutical industry. We value collaboration, innovation, and creative thinking, and are looking for talented medical writers and editors to join our team. We offer a full-time, remote position for an Editor II/Senior Regulatory Editor. Candidates should be highly proficient in MS Word and English grammar, detail-oriented, able to work independently, and flexible to meet tight, shifting deadlines.
At the Editor II level, 1-3 years of experience editing scientific data within the pharmaceutical industry, proficiency with Style Guides and/or the AMA Manual of Style, and experience with eCTD publishing are required. Our compensation is competitive: a full-time Regulatory Editor II starts at $70,000 per year, and a Senior Regulatory Editor starts at $80,000 per year, plus benefits and bonus. Actual salary depends on experience.
If you're interested in joining our team, please send your resume along with a brief description of your passion for editing.