Clinical Science Specialist/Manager

4 C Medical Technologies•Maple Grove, MN

22h

About The Position

We are looking for a motivated Clinical Science Manager with expertise and support in scientific data analysis, literature searches, medical and technical writing, scientific presentation preparation, etc. This role involves building and maintaining a comprehensive understanding of scientific/clinical data and literature related to 4C Medical and potential competitor products and disease areas. The position will assist in researching and writing clinical data related documentation for clinical, regulatory, and other functional areas, and support R&D with planning, managing, and execution of pre-clinical studies. Additionally, the role will assist in the development and maintenance of Science Affairs standard operating procedures, present summaries of relevant information from scientific meetings/conferences, and aid in planning, organizing, and executing various meetings to ensure efficacious product/data representation. This includes maintaining a global meeting calendar, assisting with abstract and presentation development, and monitoring/evaluating potential scientific analysis to recommend appropriate scientific meetings for presentation.

Requirements

Master’s degree in Science or a related field.
0 to 3 years of related scientific experience
Must have experience assist with writing, reviewing, editing, submitting, completing and obtaining peer-reviewed manuscripts.
Strong writing, teaching and presentation skills.
Excellent organizational skills and ability to handle multiple priorities in a fast-paced environment.
Able to prioritize work to meet business deadlines.
Interpersonal savvy with the written and verbal communication skills necessary to interact with study site personnel and physicians.
Ability to work independently and take directions from others is required.
Knowledge of cardiovascular anatomy and structural heart defect, disease and disorders
Advance skills in Microsoft Office Suite.
Ability to travel up to 25%

Nice To Haves

PhD in a related field is preferred.
Knowledge of endovascular devices and techniques, current interventional practices and procedures preferred.

Responsibilities

Build, maintain and demonstrate a comprehensive understanding of scientific/clinical data and literature related to 4C Medical and potential competitor products, disease areas, etc.
Assist in researching and writing clinical data related documentation for clinical, regulatory and other functional areas.
Support R&D with planning, managing and execution of pre-clinical studies.
Assist in the development and maintenance of Science Affairs standard operating procedures, as needed.
Present summary of relevant information from scientific meetings/conferences for internal team.
Aid in planning, organizing and executing various meetings to ensure the most efficacious product/data representation.
Maintains at least a year in advance global meeting calendar (including abstract submission deadlines).
Assist with preparing abstracts and subsequent presentations development based on physicians’ guidance.
Take initiative in monitoring and evaluating current and future potential scientific analysis then researching and recommending appropriate scientific meetings for presenting such analysis.