Senior Medical Affairs Specialist

Senior Medical Affairs Specialist - Contract - Acton, MA Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation! Proclinical is seeking an experienced Senior Medical Affairs Specialist to join a collaborative team dedicated to showcasing the clinical impact of innovative diabetes technologies. Primary Responsibilities: Working closely with a range of cross-functional stakeholders, you will play a key role in communicating scientific and clinical evidence, supporting evidence-generation activities, and ensuring alignment with global regulatory and compliance requirements. This opportunity is well suited to an individual with a strong understanding of diabetes management and related technologies, exceptional communication skills, and a genuine passion for advancing patient care and outcomes. Skills & Requirements: Strong understanding of diabetes and diabetes technologies, such as insulin pumps and continuous glucose monitoring systems. Proven ability to interpret and communicate clinical evidence to diverse audiences. Familiarity with global Medical Affairs best practices and healthcare compliance guidelines. Excellent written and verbal communication skills. Proficiency in relevant software tools, including Microsoft Office Suite, Adobe products, and medical communication platforms. Strong organizational skills with attention to detail and the ability to manage multiple projects in a fast-paced environment. Demonstrated leadership and collaboration skills across cross-functional and cross-cultural teams. High ethical standards in interactions with healthcare professionals and industry representatives. Educational background in a health-related field (Bachelor's degree required; advanced degrees or certifications in diabetes education preferred). Experience in clinical, industry, or research settings, with a focus on diabetes or related fields, is highly desirable. The Senior Medical Affairs Specialist's responsibilities will be: Develop and deliver medical responses to healthcare providers' inquiries, including off-label questions, while adhering to local regulations and global standards. Review global clinical promotional materials to ensure medical and scientific accuracy, compliance, and adherence to regional regulations and industry guidelines. Strategize and contribute to evidence generation plans to support innovation, regulatory submissions, and product claims. Collaborate with external vendors to implement and optimize data management systems in compliance with regulatory standards. Create and execute data dissemination plans to communicate the clinical value of products to diverse audiences, including healthcare providers, patients, investors, and regulatory bodies. Analyze clinical evidence related to diabetes therapies and technologies to inform product development and commercial strategies. Partner with Clinical and Regulatory Affairs teams to develop clinical summaries for global regulatory submissions. Establish and maintain clinical quality standards to align with global practices. Plan and execute activities for scientific conferences, including presentations, reports, and medical information booths. Provide mentorship to Medical Affairs interns. Compensation: $75 to $86 per hour. #J-18808-Ljbffr Proclinical