Senior Medical Writer – Client Aligned (FSP)

ThermoFisher Scientific; España; A distancia; EUR 65.000 - 95.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe. We seek a Senior Medical Writer to develop high-quality regulatory documents for a client in the FSP space, with experience in structured content authoring and automation to support delivery.

The role involves leading complex medical writing projects, mentoring junior writers, and ensuring compliance with regulatory requirements and company standards across clinical study reports and regulatory submissions.

Formación

• Bachelor's degree in a scientific discipline required; advanced degree preferred.
• 5+ years regulatory writing experience in pharma/CRO environments.
• Experience developing clinical/regulatory documentation compliant with guidelines.
• Ability to lead complex medical writing projects and mentor peers.

Responsabilidades

• Write and edit clinical and regulatory documents including CSRs, protocols, investigator brochures, and submissions.
• Collaborate with cross-functional teams to gather information and ensure accuracy of documents.
• Ensure alignment with regulatory guidelines and company standards in all deliverables.
• Provide input on document content, structure, and presentation.
• Review documents prepared by others and provide actionable feedback.
• Manage timelines and deliverables for assigned projects.
• Mentor junior medical writers and ensure high-quality outputs.

Conocimientos

Regulatory writing

Clinical trial docs

Protocol writing

Cross-functional collaboration

Mentoring junior writers

Educación

Bachelor's degree in a scientific discipline

Advanced degree preferred

Descripción del empleo

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. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. 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.

Summarized Purpose:

We are excited to be expanding our Medical Writing FSP Team in Europe. We are looking for a SMW to be dedicated to a client in the FSP space; experience in Structured Content Authoring systems and automation to support delivery would be preferred. We are seeking a talented and experienced Senior Medical Writer to join our team. The Senior Medical Writer will be responsible for developing high-quality clinical and regulatory documents, ensuring they meet all regulatory requirements and company standards.

Key Responsibilities:

• Write and edit clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.

• Collaborate with cross-functional teams to gather necessary information and ensure the accuracy and completeness of documents.

• Ensure documents align with regulatory guidelines, company standards, and industry best practices.

• Provide input on document content, structure, and presentation.

• Review and provide feedback on documents prepared by other team members.

• Manage timelines and deliverables for assigned projects.

• Mentor and provide oversight to junior medical writers and ensure high-quality deliverables

• Stay current with industry trends, guidelines, and regulatory requirements.

Education and Experience:

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred.

• Regulatory writing experience that provides the knowledge, skills, and abilities to perform the role (comparable to 5+ years).

• Experience working in the pharmaceutical/CRO industry required.

• Experience in managing and directing complex medical writing projects required.

• EU CTR experience preferred.

Knowledge, Skills, and Abilities:

• Excellent organizational and program management skills.

• Proven leadership skills to manage and mentor a team of medical writers.

• Extensive knowledge of regulatory guidelines and drug development processes.

• Strong interpersonal and communication skills to build and maintain effective working relationships with colleagues and stakeholders.

• Understanding of quality control processes to ensure compliance with regulatory requirements and internal standards.

• Self-motivated and adaptable.

• Excellent judgment; high degree of independence in decision making and problem solving.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.