[Innovative Medicine] R&D, Associate Medical Writer, Medical Writing Group 3, Regulatory Affairs Div.

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. 

• Writes and coordinates clinical documents
• Participates in cross-functional document planning and review meetings
• Works in a team environment with some guidance provided and takes a somewhat active role on assigned projects with respect to timing, scheduling, and tracking

Qualifications

Principal Relationships:

Internal (as collaborator and peer): manager, other writers, cross-functional contacts (eg, clinical regulatory, or biostatistical functions) involved in the planning and preparation of clinical documents.

External: May interact with contractors or external service providers as needed, under close supervision.

Education and Experience Requirements:

• A university/college degree is required. An advanced degree (eg, Masters, PhD, MD) is preferred.
• At least 2 years of relevant pharmaceutical/scientific experience is required.

Other:

• Solid oral and written communication skills.
• Attention to detail.
• Ability to function in a team environment.
• Organizes time well.
• Demonstrates learning agility.
• Builds solid and productive relationships with cross-functional team members.
• Learns how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content, under close supervision.