Responsibilities

• Write clear, compelling, and compliant promotional copy for HCP, payer and/or DTP audiences across global and local projects, with increasing ownership over content across tactics.
• Translate complex scientific and clinical data into accessible messaging that aligns with brand strategy and regulatory requirements.
• Develop copy for digital, print, social, video, IVAs, MOAs, websites, congress and more – ensuring a consistent brand voice and clear message hierarchy.
• Collaborate cross-functionally with Creative copywriters, Art Directors, Strategists, and Medical/Regulatory to ensure alignment on scientific accuracy, story flow, and execution feasibility.
• Ensure all copy is properly referenced, annotated, and submission-ready per guidelines.
• Support concept development and early-stage ideation, offering strategic messaging input and bold copy explorations.
• Participate in internal reviews, client meetings, and MLR (Medical, Legal, Regulatory) discussions to advocate for the work and navigate feedback constructively.

Requirements

• A confident writer with experience in healthcare or pharmaceutical advertising, including medical or scientific content.
• Comfortable working within regulatory and compliance frameworks, with a solid grasp of claim structure, referencing, and label interpretation.
• Curious and rigorous—someone who dives deep into disease areas and clinical data to write accurately and persuasively.
• Detail-oriented and deadline-driven, managing multiple assignments with focus and follow-through.
• A collaborative teammate who thrives in a fast-paced, multi-disciplinary environment and enjoys taking on new challenges.
• 2yrs+ of experience in medical or pharmaceutical copywriting, ideally in an agency setting.
• Working knowledge of MLR submission processes and promotional requirements.
• Demonstrated ability to write for multiple audiences (HCP, payer, DTP) and formats (emails, websites, IVAs, video scripts, congress etc.).
• Life science degree preferred, but advertising, communications or journalism, considered.

Preferred

• Experience in rare disease, oncology, or high-science therapeutic areas
• Confidence navigating MLR meetings and advocating for approvable messaging
• Familiarity with Ziflow and Veeva or similar platforms used in pharma review processes

Benefits

• Dynamic Working
• Personal Development fund
• Generous holiday allowance
• Cycle to work scheme
• Pension contribution
• Various health and wellbeing benefits available
• Online training platform/programs
• Discretionary bonus scheme
• Community action focussed programs