ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment. With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product lifecycle.
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment. With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product lifecycle. A Medical Writer will author regulatory, clinical trial and medical affairs documentation. Additionally, the Medical Writer will contribute to medical writing knowledge to new business proposals. Essential Functions Include: High quality regulatory writing including authoring clinical summaries, briefing documents and investigation plans for submissions. Represent Medical Writing on project teams and, as such, advise teams and clients on content and format requirements for various documents, as well as coordinate writing activities for document development. Ensure compliance, remain informed on regulations and developments in medical writing. Maintain knowledge of product areas, current trends, and current literature. Providing general scientific insight for new business pitches and proposals.Qualified candidates must have: Postgraduate degree in a life sciences discipline Regulatory submission experience Good working knowledge of the healthcare and pharmaceutical industry Excellent interpersonal skills Keen attention to detail Flexibility to move quickly between projects and work across different therapy areas A positive can-do attitude Ability to work independently but contribute pro-actively to a project teamWe celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More
