![]() In 2016, I got a job at a clinical research organization, managing trials for drug companies.Īfter that, I took my first role in industry: I worked in medical affairs at a leading pharmaceutical company, where I spent three years as a medical adviser in haemato-oncology. I have always enjoyed the challenge of learning something new, and you get that motivation in the pharmaceutical industry, because you’re always learning and applying your knowledge. ![]() But I didn’t want to leave medicine altogether because of the big commitment I’d already made. I loved my job as a doctor and treating patients, but I had never been one of those people who had wanted to be a doctor ever since they could remember. Soon after qualifying as a medical doctor in 2010, I started thinking about alternative careers - not because I wasn’t enjoying medicine, but because I was looking at everything that motivates me in and out of work, and I wondered whether something was missing. Here, he offers advice on making the change, culture shock and the tricky business of negotiating a pay rise. ![]() In 2020, he and a colleague founded, an online mentoring resource that helps scientists and clinicians to navigate moving from academia, medicine and health professions into pharma. Jonathan Bowen left clinical medicine in 2016 for a role in the pharmaceutical industry and is now drug company Sanofi’s medical lead for haemato-oncology, in Reading, UK. ![]() Softworld has developed expertise across six distinct staffing and consulting practices over the past 25 years that include Technology Services, Life Sciences, Engineering, Government, Banking, and Creative Services.Moving from an academic lab to an industry one can be a culture shock. Softworld, Inc., a 2018 Inavero Best of Staffing Award Winner for both talent and client satisfaction, is a multifaceted staffing and consulting firm with the experience and infrastructure to support clients and talent on a national level. Subcontracting is not available for this position. Applicants received from firms will not be considered. THIRD PARTY AGENCIES, SUBCONTRACTORS, AND RECRUITERS NEED NOT APPLY. * Good communication, interpersonal, and team skills. Microsoft office, and expertise with EndNote or equivalent. * Experience working with different document management tools, ie. * Minimum 4-6 years relevant professional experience in Medical Writing. * Knowledge and understanding of the clinical research process, including ICH GCP, and FDA/EMA/NMPA guideline for clinical study. Publications in the international journals as the first author would be a plus. * Master's degree or above, majoring in medicine, pharmacy, or life science related disciplines. * May oversee external vendors to provide writing service for internal AHT projects. * Arranges and conducts review meetings with team, and coordinates responses to inquiries, questions, and deficiencies received from submission reviewers. * Acts as interface to resolve issues and questions arising during writing process. * Communicates deliverables needed and writing process to team members. * Utilizes submission templates (if available) or format/style guidelines (if available) according to related SOP. * Serves as the Medical Writing representative on product teams. * Relative Clinical/regulatory review documents Top Required Skills - 5 years industry experience, focus on medical writing oncology, small molecule, IND & NDA experience, provide guidance to internal medical/clinical science teamīe responsible for preparation of key clinical documents for regulatory submissions and other documents not limited to below:
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