ProEd Communications is a healthcare communications firm located in Beachwood, Ohio. ProEd has extensive experience developing data dissemination programs for pharmaceutical products at all stages of clinical development through post-marketing. At the heart of our scientific services is the development of evidence-based scientific content. Our scientists are among the best in the world and strive to understand the nuances of product data and disease states to develop relevant and viable scientific content for a variety of audiences, venues, and communication vehicles.
ProEd is adept at coordinating all aspects of events for a wide range of medical communications needs. This combination of meetings and medical expert management is a unique strength when combined with our depth of scientific content development experience. Additionally, ProEd has formed national and global publication partnerships with noteworthy journals and medical congresses, and these relationships routinely provide insight and guidance to ProEd and our clients.
ProEd is a member of the Healthcare Consultancy Group (HCG) which serves the pharmaceutical, biotech, and device industries by providing strategic, scientific communications solutions at all stages of the product lifecycle. Part of Omnicom’s Diversified Agency Services (DAS), HCG is a leader in the healthcare segment with over 350 employees, including more than 90 advanced degree scientists (MD, PhD, or PharmD). We are scientifically rigorous, strategically focused, creatively balanced agency built for the future.
Position requires a motivated and detail-oriented scientist with outstanding communications skills. Applicant will join our team of experts in preparing pharmaceutical, biotech, and device company clients for successful regulatory submissions and health authority meetings.
Current, hands-on experience in the preparation of critical regulatory documents and presentations
Experience working in a consulting or agency environment collaborating with multiple clients in diverse therapeutic areas
Experience preparing for EMA Oral Explanations and/or FDA Advisory Committee meetings, and developing Target Product Profiles/regulatory strategy is preferred
In-depth knowledge and understanding of regulatory/compliance guidelines, submission requirements, and best practices
Good understanding of the clinical development process
Team player able to collaborate with a team of medical writers and editors, project managers, and strategic consultants to service clients in a project-based environment
Willingness to participate in new business development activities
Willingness to travel up to 25%, including occasional weekend travel
Advanced degree in the life sciences
No less than 5 years of experience in the development of critical regulatory and clinical documents and/or regulatory affairs
Demonstrated track record of commitment to excellence in technical skills, client relations, problem solving, and collaboration with colleagues
Healthcare Consultancy Group (HCG) serves the pharmaceutical, biotech, and device industries by providing strategic, scientific communications solutions at all stages of the product lifecycle. HCG’s nine companies have unique capabilities and cultures, yet share a philosophy that puts our clients’ drugs at the center of all we do. Part of Omnicom’s Diversified Agency Services (DAS), HCG is a lead...er in the healthcare segment, with over 350 employees, more than 90 with advanced degrees (MD, PhD, or PharmD). We are a scientifically rigorous, strategically focused, creatively balanced agency built for the future.