Work Schedule Standard (Mon-Fri)Environmental Conditions Office Job Description At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies.

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. We are excited to expand our Medical Writing FSP Team in Europe This would be a remote role.

We are looking for a Principal Medical Writer to be dedicated to a client in the FSP space; As a Principal Medical Writer you will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.

As the lead writer, you will review documents for the team and provide training and guidance to junior team members.

Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies. Provides senior level review of routine and complex documents.

Provides training and mentorship for other writers and program managers on document preparation, the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge. Ensures compliance with quality processes and requirements for assigned documents.

May also develop, review, and manage performance metrics for assigned projects.



Represents the department at project launch meetings, review meetings, and project team meetings. Education and Experience: Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Experience in managing and directing complex medical writing projects required Experience working in the pharmaceutical/CRO industry preferred Submissions document experience advantageous Experience in Neurosciences advantageous Additional qualifications in medical writing (AMWA; RAC) advantageous Knowledge, Skills, and Abilities: Significant knowledge of global, regional, national,

Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills Excellent project management skills Advanced interpersonal, oral, and written communication, and presentation skills Excellent negotiation skills Excellent judgment; high degree of independence in decision making and problem solving Ability to mentor and lead junior level staff. What We Offer: At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team.

We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.

We have a flexible working culture, where PPD clinical research services truly value a work-life balance.

We are a integral organization but with a local feel. Integrity, Intensity, Innovation, and Involvement

- working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. FSP Principal Medical Writer (Regulatory) - Client-Dedicated (España)

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📌 Senior Medical Writer Remote (Málaga)
🏢 Sin nombre
📍 Málaga