
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Yesterday

Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Manage, mentor, and develop Medical Writers to ensure exceptional performance and continuous growth • Oversee workload distribution, resource planning, and project assignments • Conduct regular 1:1s, performance reviews, and coaching conversations • Supervise and review the preparation of a wide range of medical writing deliverables • Ensure projects are completed on time and to the highest scientific and regulatory standards • Serve as a senior reviewer and departmental expert for study design, adverse event reporting, and interpretation of statistical data • Stay current with ICH, FDA, and global regulatory guidance • Deliver compelling capabilities presentations to prospective clients • Collaborate with Business Development and Contracts teams to support bids, budgets, and proposals • Contribute to the development, evaluation, and improvement of SOPs and work practices • Lead or support internal training programs to ensure new and existing staff are well-equipped for success
• Bachelor’s degree in a life science field (advanced degree—PharmD, PhD, MSc—preferred) • 5+ years of relevant regulatory writing experience, including at least 2 years in medical writing within pharma/CRO and 1+ year of leadership responsibility • Exceptional writing, editorial, and data interpretation skills • Strong project management ability—forecasting, timelines, resource allocation • Excellent communication and presentation skills, especially in client-facing settings • Ability to manage complexity, multitask, and work in a fast-paced environment
• award-winning learning and development programme • competitive salary • extensive benefits package • flexible working culture • valuing work-life balance
Apply Now2 days ago
Lead a team of scriptwriters at Hostinger, creating engaging YouTube content that boosts online presence. Collaborate across teams for impactful storytelling and optimize for audience engagement.
October 31
Senior UX Writer crafting clear UI content for UserTesting's platform. Ensuring language clarity and user engagement through collaboration with design, product, and engineering teams.
July 29
Oversee medical writing projects and lead a team to maintain quality at Syneos Health.