Sr. Writer (Medical Information) - Evidera

Thermo Fisher Scientific; Roma; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading scientific firm is seeking a Sr. Writer, Medical Information to join their remote team. This role involves independent research and writing of medical materials, mentoring other writers, and ensuring regulatory compliance. Candidates should have a Bachelor's degree in a scientific field and at least 5 years of relevant experience in the pharmaceutical or CRO industry. Join a company focused on making the world healthier, cleaner, and safer.

Competenze

• 5+ years of relevant experience in medical information writing.
• Experience in the pharmaceutical/CRO industry preferred.
• Additional qualifications in medical writing advantageous.

Mansioni

• Conduct independent research and editing of medical writing materials.
• Mentor other writers and handle project planning.
• Ensure documents meet scientific accuracy and compliance.

Conoscenze

Medical writing

Project management

Analytical skills

Conflict resolution

Formazione

Bachelor’s degree in a scientific field

Descrizione del lavoro

Sr. Writer, Medical Information - Evidera

We are looking to fill this role remotely, in any of these locations: UK, Spain, France, Italy, Sweden.

At Thermo Fisher Scientific, you’ll 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.

Responsibilities

• Independent research, writing, and editing of standard medical information writing materials (global or regional standard response documents, custom responses, and FAQs) across various therapeutic areas.
• Independently writes more complex medical writing materials and provides senior review of documents.
• Train and mentor other writers; handle all aspects of planning, organizing, and completing projects without supervision, including developing project timelines, standards, budgets, forecasts and contract modifications.
• Identify out-of-scope activities and propose solutions; may lead several long-term projects concurrently.
• Interact with internal and external personnel on significant matters requiring cross-functional coordination.
• Represent the department as a primary contact on projects, including Project Launch Meetings, Review meetings, client audits, bid defenses, and capabilities presentations; establish and develop client relationships; assist with business development and budgeting/proposals.
• Ensure documents are clear, concise, compelling, scientifically accurate, and aligned with regulations, industry standard processes, and corporate guidance.

Qualifications and Experience

• Bachelor’s degree in a scientific field or equivalent qualification.
• Proven experience as a Medical Information Writer, with at least 5+ years of relevant experience.
• Experience in the pharmaceutical/CRO industry is preferred.
• Additional qualifications in medical writing (AMWA; EMWA; RAC) are advantageous.
• Able to work with and format numbers and data accurately to provide evidence and insights.
• Ability to analyze complex issues, identify cause-effect relationships, and generate effective solutions.
• Ability to manage project plans, lead team members, monitor progress, and deliver results.
• Sound professional judgment in analyzing, responding to, and resolving inquiries and customer concerns.
• Ability to facilitate conflict resolution among team members and clients.

Physical Requirements / Work Environment

• Normal and routine office duties; travel domestically and internationally may be required.

Our Mission and Equal Opportunity Statement

Our Mission is to enable our customers to make the world healthier, cleaner and safer. 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, age, disability, or veteran status.