We are currently seeking a talented, scientifically strong, and entrepreneurial spirited individual who is interested in growing with the company, for the role of Medical Affairs Associate Consultant, reporting to the company CEO. This is an important role in which you will interface with various clients in a variety of medical affairs related projects such as medical writing, medical communication, research and analysis of publications, KOL engagement, contribution to the medical and health economic related projects, presentations, and training programs. As a consulting firm who supports startups to large corporations in different stages, our projects involve a range of medical and scientific topics, and strategic and operational nature. Success in this role requires flexibility, agility, and high professional integrity.
Role starts as casual part time with opportunity for growth for successful candidate.
Your Responsibilities: • Writing and editing of all or parts of medical writing projects including manuscripts, white papers, clinical evaluation reports • Research literature using primary and secondary sources, and extract pertinent data • Translate published data into compelling and accurate clinical messaging • Review clinical cases and identify documentation gaps • Create impactful presentations and training material • Respond to client inquiries • Follow up on projects and ensure timeliness • Support clinical and regulatory projects • Support facilitation of client workshops or conference calls • Create, edit, word process, and update PowerPoint decks, Excel spreadsheets, and Word documents • Contribute to strategic discussions and client discovery calls as needed • Interface with the clients, understand and complete their projects in a professional manner • Help create and update company standard operating procedures • Document all work in a careful, accurate and compliant manner • Comply with and follow all laws, rules, and regulations, codes, guidance documents and policies associated with pharmaceutical and medical device industry Your Acumen: • Understanding the clinical and business implications of technically complex products and services • Strong understanding and technical skills to communicate and work in the virtual environment • Adaptability for taking on variety of projects • Willingness to operate at a range of levels depending on project, client, and business needs • Ability to work remotely or onsite as business and clients require • Clear and frequent communication within the company and with clients • Solid understanding of the medical device and pharmaceutical industry • Excellent interpersonal and communication skills • Self-starter effective with minimal supervision • High degree of integrity, confidentiality, and ethics • International experience a plus Your Qualifications: • Advanced degree in medical or scientific discipline. MD preferred. • 5+ years of experience in the medical device or pharmaceutical industry in Medical Affairs, Medical Communication or Clinical Development role • 3 years of experience with writing or editing medical scientific content, including clinical evaluation reports, manuscripts, clinical study protocols, clinical study reports • Proficiency with Microsoft Office tools such as Microsoft Word, Outlook, PowerPoint, Excel • Experience using scientific databases to search for published literature • Familiarity with regulatory requirements for medical device and pharmaceuticals • Canadian permanent residency or citizenship