Job Description Senior Medical Writer (EMEA) (FSP; Remote) 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.
Summarized Purpose: We are excited to expand our Medical Writing FSP Team in EMEA!
This would be a remote role working from any location in EMEA.
We are looking for a Senior Medical Writer to be dedicated to a client in the FSP space; experience in Immunology, Oncology or Vaccines would be valuable but not essential.
As a Senior Medical Writer within the FSP team, you will provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
Essential Functions: Serves as primary author for FSP clients who writes and provides input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.
May research, write or edit complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
Reviews routine documents prepared by junior team members and may provide training and mentorship for junior writers.
Ensures compliance with quality processes and requirements for assigned documents.
May assist in program management activities, including developing timelines, budgets, forecasts, and contract modifications.
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; Advanced degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
Experience working in the pharmaceutical/CRO industry preferred.
Experience working within FSPs preferable.
Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, and Abilities: Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills.
Strong project management skills.
Excellent interpersonal skills including problem solving.
Strong negotiation skills.
Excellent oral and written communication skills with strong presentation skills.
Significant knowledge of global, regional, national, and other document development guidelines.
In-depth knowledge in a specialty area such as preclinical, therapeutic, regulatory submissions, communications, etc.
Great judgment and decision-making skills.
Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g., Excel, Outlook).
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.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees.
We have a flexible working culture, where PPD clinical research services truly value a work-life balance.
We have grown sustainably year on year but continue to offer a collaborative environment.
Our Mission is to enable our customers to make the world healthier, cleaner, and safer.
As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement.
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