Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunities for professional growth and development. And the best part? It\xe2\x80\x99s fully remote, allowing you to work from anywhere in the UK, Israel, or Germany.Responsibilities:\xe2\x80\x93 Write and/or edit various clinical regulatory documents: As a Senior Regulatory Affairs Writer, you will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs, Protocols, Summaries, Briefing Books, Pediatric Plans, and Model 2 summaries for submissions. Your expertise in driving project consensus and foreseeing potential issues will be highly valued
\xe2\x80\x93 Oversee and mentor: Take on a leadership role and oversee outsourced writing deliverables. Provide guidance, support, and strategic assistance to the team. You\xe2\x80\x99ll be responsible for ensuring that clinical documents are accurate, complete, and adhere to regulatory guidelines and company standards
\xe2\x80\x93 Collaborate and communicate: Be a clear communicator and a team player. You\xe2\x80\x99ll work in a cross-functional environment, collaborating with various teams and stakeholders. Your ability to effectively communicate and drive project consensus will be key to your success in this roleRequirements:\xe2\x80\x93 Life sciences background: A PhD/PharmD in life sciences (or related field) with a minimum of 5 years of experience, or a Master\xe2\x80\x99s degree in life sciences (or related field) with a minimum of 7 years of experience
\xe2\x80\x93 Willingness to learn and grow: Our client is looking for a motivated candidate who is eager to learn and grow as part of a team. While extensive experience is not required, a willingness to continuously develop your skills and contribute to the team\xe2\x80\x99s success is essential
\xe2\x80\x93 Problem-solving skills: As a Senior Regulatory Affairs Writer, you\xe2\x80\x99ll need to be a proactive problem solver. Your ability to anticipate issues, drive project consensus, and find solutions will be crucial in this roleBenefits:\xe2\x80\x93 Competitive compensation package: Our client understands the value of your skills and expertise. They offer a highly competitive compensation package that reflects your experience and contribution
\xe2\x80\x93 Professional growth and development: As a Senior Regulatory Affairs Writer, you\xe2\x80\x99ll have the opportunity to work on a diverse range of projects, from writing and editing clinical regulatory documents to providing oversight for outsourced deliverables. You\xe2\x80\x99ll be able to enhance your skills and broaden your knowledge in the field of medical research
\xe2\x80\x93 Stimulating work environment: Join a team at the forefront of medical research, where every day brings new challenges and opportunities to make a difference. Collaborate with cross-functional teams and contribute to the development of crucial clinical regulatory documents that impact the advancement of medical science.Apply now and become a part of this exciting journey!Interested? Don\xe2\x80\x99t miss out on this exciting opportunity! Apply today and take your career to new heights. Send me a copy of your CV in Word format or share as this is a great opportunity for the right person! This is a 1 year contract and the client is looking for someone to start as soon as possible so please share your CV if interested, Forward to Oksana at O.Kolesnichenko@nonstop-recruitment.com or via linked in.The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles.NonStop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus.
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