Serving as a link among key functions, the Scientific Communications Senior Medical Writer ensures that critical information is communicated with clarity, precision, and accessibility. By interpreting clinical study results and collaborating with HCPs (e.g., study investigators, physicians, KOLs) and cross-functionally with Clinical Research, Regulatory Affairs, R&D, Marketing and other groups, the Scientific Communications Senior Medical Writer will work to prepare journal manuscripts and conference proceedings (e.g., abstracts and presentations), to support product development and marketing. The Scientific Communications Senior Medical Writer may contribute to tracking medical writing documents, developing templates, and training new staff. This position is open to well-qualified candidates throughout the US.

• Prepare abstracts and presentations for submission and presentation at conferences.

• Engage in scientific writing and/or edit manuscripts for submission to peer-reviewed

journals to achieve publication goals.

• Develop and cultivate strong relationships with academic institutions, physicians, KOLs,

hospitals, and scientific societies/associations to facilitate scientific communication efforts.

• Contribute to the preparation of clinical data for analysis and report writing.

• Keep current and conduct literature searches for relevant disease states and maintain the

clinical literature library.

• Attend relevant medical and scientific conferences to synthesize and disseminate the

summaries.

• Lead cross-functional project reviews and serve as a subject matter expert on clinical study

teams to create timelines for completing of medical writing documents.

• Lead cross-functional project reviews and serve as core team member on clinical study

teams.

• Adhere to the Company’s Quality Management System (QMS) as well as domestic and

global quality system regulations, standards, and procedures. *

• Understands relevant security, privacy and compliance principles and adheres to the

regulations, standards, and procedures that are applicable to the Company. *

• Ensure other members of the department follow the QMS, regulations, standards, and

procedures.*

• Perform other work-related duties as assigned.

*Indicates an essential function of the role

• Bachelor's degree in a scientific or health-related discipline is required with 3+ years of

experience as a Medical Writer in the biotech/pharmaceutical industry or 5+ years of

experience in clinical/scientific research, nursing, or an equivalent combination of education

and experience.

• Willingness and ability to travel up to 20%.

• Advanced degree highly desired.

• Medical device, pharmaceutical, biotech, or other regulated industry experience desired.

• A background in the cardiovascular space is highly desired.

• A passion for clarity in written expression.

• A style that is equally comfortable working independently and as part of a team.

• A body of work that demonstrates outstanding writing skills.

• High degree of accuracy and attention to detail.

• Proficiency with MS Word, Excel, and PowerPoint.

• Excellent organizational skills with ability to prioritize assignments while handling various

projects simultaneously.

• Familiarity with laws, regulations, standards, and guidance governing the conduct of clinical

studies a plus Excellent organizational skills with ability to prioritize assignments while

handling various projects simultaneously.

• A collaborative teamwork environment where learning is constant and performance is rewarded

• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases

• A generous benefits package that includes medical, dental, vision, and life insurance; a 401(k) match; and an Employee Stock Purchase Plan

For additional information on Penumbra’s commitment to being an equal opportunity employer, please see Penumbra's AAP-Policy-Statement.