LanceSoft
Sr Med Science Writer - Exempt Job at LanceSoft in Mounds View
LanceSoft, Mounds View, MN, US
HM's Top Needs:
Years' Experience Required: 4 years (or 2 with advanced degree)
Work Schedule: 40 hours a week
Work Location: Mounds View
On-site Requirement: Yes, 4 days starting in September
Responsibilities
- Experience with peer-reviewed manuscript development from clinical research/studies
- Strong writing skills
- Project management
Years' Experience Required: 4 years (or 2 with advanced degree)
Work Schedule: 40 hours a week
Work Location: Mounds View
On-site Requirement: Yes, 4 days starting in September
Responsibilities
- Lead publication plan development and produce scientific content aimed at external audiences to maximize awareness and accessibility.
- Write, edit, and format manuscripts, abstracts, and scientific presentations in collaboration with authors and contributors.
- Develop an in-depth knowledge of key therapy and product areas, staying abreast of current literature relevant to CRM therapies and products, including competitors.
- Compile, analyze, and summarize data for each writing project.
- Collaborate with physicians, clinical and statistics teams to plan and identify appropriate analysis plans.
- Oversee individual publication activities, ensuring compliance with publication processes and procedures for *** and target journals.
- Create scientific messages to simplify complex information and maximize awareness for scientific audiences.
- Analyze and optimize content based on feedback and input from stakeholders and/or metrics.
- Create and manage the project schedule for each deliverable through final delivery (e.g., peer-review publication, scientific conference presentation) while ensuring compliance with regulatory, medical society, and corporate standards.
- Interface with physicians, clinical leadership, and other stakeholders to align evidence dissemination activities and deliverables.
- Lead, coordinate, and/or participate in Publication Committee meetings and administer follow-up actions (e.g., document decisions).
- Support team activities at medical device congresses, as assigned, which may include attending publication planning meetings with investigators in *** clinical trials, executing *** sponsored symposia, and covering relevant scientific sessions.
- Maintain files on informative journal abstracts according to current or estimated future needs.
- Track and report on metrics related to CRM medical writing services to clinical leadership and key business partners.
- May serve as a medical/scientific consultant to marketing or research project teams and external stakeholders.
- May assist study personnel in providing interim and final reports and presentations.
- May manage a portfolio of publication activities on assigned projects (e.g., collect input on strategic alignment, drive commitment decisions, communicate decisions to investigators).
- May participate in process improvement initiatives, including the need to create new tools, repositories, etc.
- Bachelor's degree required
- Minimum of 4 years of clinical/medical/scientific writing experience or advanced degree with a minimum of 2 years of clinical/medical/scientific writing experience