Raw Power Games

Unsolicited Application

Raw Power Games is looking for talented individuals to join their team, even without a specific job opening. They are a games developer focused on creating amazing games while fostering a remarkable work culture. They offer flexible work hours, remote options, and prioritize task completion over specific time or location. The company is fully funded to develop and release the first game early 2026 with an expected size of 75-85 employees. They believe in an inclusive and inspiring work environment, resulting in exceptional games. They encourage experimentation and recognize the value of learning and growth.

Why submit a Spontaneous Application to Raw Power Games?Even if you don't see a current opening that matches your profile, we're always on the lookout for talented individuals who can contribute to our mission. By submitting a spontaneous application, you:<ul> <li>Express your interest in joining our team</li> <li>Allow us to consider you for future opportunities</li> <li>Showcase your unique skills and experiences</li> </ul> Raw Power Games is a games developer dedicated to creating amazing games while fostering a remarkable work culture for our team. At Raw Power Games, we encourage experimentation and recognize the value of learning and growth. We are located in Copenhagen, but with flexible work hours and remote options, we prioritize task completion over specific time or location. We believe that an inclusive and inspiring work environment brings out the best in our talented individuals, resulting in exceptional games.&nbsp;The company is fully funded to develop and release the first game early 2026 with an expected size of 75-85 employees - the majority being industry veterans. We strive to be the best workplace in the games industry, by offering:&nbsp;<ul> <li>Competitive salaries</li> <li>Supplemental pension contributions</li> <li>Generous revenue share</li> <li>30 days of annual vacation</li> <li>Flexible work hours, remote when you need to</li> <li>Remote work supported (if the timezone is plus/minus 1/2hrs from Copenhagen)</li> <li>Flat hierarchy</li> <li>Great focus on work/life balance</li> <li>Bleeding edge tech stack</li> <li>Skilled co-workers that are driven by a passion to create</li> </ul> Diversity and Culture We strongly believe in a discrimination-free workplace. Harassment, bullying, and exclusionary practices are not tolerated. We embrace the diversity of experience, perspectives, and background - they help us create a people-positive work environment and engaging games.

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General SummaryServing as a key link among essential functions, the Scientific Communications Medical Writer ensures the clear, precise, and accessible communication of critical information. By interpreting clinical study results and collaborating with healthcare professionals (e.g., study investigators, physicians, and key opinion leaders) and cross-functional teams within clinical research, regulatory affairs, research and development, and marketing, the medical writer will prepare journal manuscripts and conference materials (e.g., abstracts and presentations) to support product development and marketing efforts. Additionally, the medical writer may contribute to tracking medical writing documents, developing templates, and providing training for new staff members. "Unfortunately, sponsorship is not available for this position. Qualified applicants must be legally authorized to work in the U.S. without the need for employer sponsorship now or in the future.Specific Duties and Responsibilities•Prepare high-quality 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.•Ensure scientific communication deliverables are completed in a timely manner.•Evaluate data and translate information into succinct, scientific summaries.•Collaborate cross-functionally with clinical, marketing, and creative teams to ensure data dissemination goals and deadlines are met.•Work with clinical study management and statistics teams to create timelines for completing data dissemination plans related to clinical studies.•Strong communication with physician authors to achieve deliverables, maintain relationships, and to facilitate overall scientific communication efforts.•Contribute to the preparation of clinical data for analysis and scientific writing.•Conduct literature searches for relevant disease states and maintain the clinical literature library.•Lead cross-functional project reviews and serve as a core team member and subject matter expert on clinical study teams to create timelines for completing medical writing documents.•Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. *•Understand relevant security, privacy and compliance principles and adhere 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 rolePosition QualificationsRequired education and experience:•Advanced degree (Master’s, PhD, or MD) with 2+ years of experience as a medical writer in the medical device, biotech, or pharmaceutical industry; or 5+ years of experience as a medical writer in clinical/scientific research, or an equivalent combination of education and experience.Additional qualifications:•Experience as a medical writer for cardiovascular clinical trials in the medical device, biotech, or pharmaceutical industries is preferred.•Demonstrates a diligent approach to work, with a portfolio that showcases outstanding writing skills and a passion for clarity in written expression.•Team player with excellent organizational skills and the ability to prioritize assignments and manage multiple projects simultaneously, both independently and collaboratively.•Proficient in Microsoft Office 365.•Familiarity with laws, regulations, standards, and guidance governing the conduct of clinical studies a plus.Working Conditions•General office environment.•Willingness and ability to work on site.•May have business travel from 5% - 10%.•Requires some lifting and moving of up to 15 pounds.•Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.•Must be able to move between buildings and floors within the office and access file cabinets or other supplies, as needed.•Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.Annual Base Salary Range $99,000 - $135,000This is the pay range for a mid-cost labor market. If hired in another region, there will be a difference in pay range. We offer a competitive compensation package plus a benefits and equity program, when applicable. Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.What We Offer•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 for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

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