Agency Profile
BGB Group is a healthcare communications agency that offers a wide range of services, including traditional pharmaceutical advertising, promotional medical education, payer marketing, and consulting services. Known for excellence and professionalism, we’re hired as strategic and creative partners by our biopharmaceutical clients to drive category/brand awareness and growth.
Position Overview
As a Group Copy Supervisor, you will lead the development of compelling, strategy-driven content for healthcare brands across multiple therapeutic areas. You will oversee a team of writers, ensuring the highest standards of medical accuracy, creativity, and compliance with regulatory guidelines. In collaboration with cross-functional teams, you will help drive brand messaging, maintain consistency, and mentor junior and mid-level writers. This role requires both hands-on writing expertise and strong leadership skills.
Role Requirements
* Lead the development of scientific and promotional content, ensuring alignment with brand strategy and compliance requirements.
* Oversee and mentor a team of copywriters, providing guidance, feedback, and career development support.
* Partner with creative, medical, and account teams to develop compelling, high-quality content across multiple channels (digital, print, video, social, etc.).
* Review and edit content for scientific accuracy, clarity, engagement, and adherence to brand voice.
* Stay up-to-date with industry trends, regulatory guidelines, and competitive landscape to inform strategic content development.
* Present content to internal teams and clients, articulating rationale and addressing feedback.
* Manage workload and workflow to ensure timely delivery of high-quality materials.
* Collaborate with medical and regulatory teams to navigate approval processes efficiently.
Preferred Qualifications
* Bachelor’s or advanced degree in Life Sciences, English, Journalism, Communications, or a related field.
* 6+ years of experience in healthcare/pharmaceutical copywriting, with at least 2 years in a supervisory role.
* Strong understanding of medical and scientific concepts, as well as experience translating complex information into compelling content.
* Familiarity with regulatory requirements (e.g., FDA, OPDP, medical/legal review processes).
* Exceptional writing, editing, and communication skills.
* Ability to multitask, manage multiple projects, and work effectively in a fast-paced agency environment.
* Experience working across a variety of therapeutic areas is preferred.
* Proficiency in Microsoft Office and familiarity with content management and collaboration tools.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other legally protected basis, in accordance with applicable law.
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