Senior Regulatory Medical Writer FSP Remote US
Senior Regulatory Medical Writer FSP Remote US
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Standard Office Hours 40/wk)Environmental Conditions
OfficeJob Description
Senior Regulatory Medical Writer (FSP; Remote; US
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 lifechanging 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 expand our Medical Writing FSP Team in the US! This would be a remote role working from any location in the US. We are looking for a Senior Medical Writer to be dedicated to a client in the FSP space; experience in Immunology or Vaccines would be valuable but not essential. As a Senior Medical Writer within the FSP team you will provide highquality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. You will collaborate with internal and external clients supporting and enabling effective and efficient communication that results in operational excellence.
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. May provide training and mentorship for junior 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. Provides input on and independently develops best practices methods and techniques for achieving optimal results including various clientspecific processes.
- May assist in program management activities. Identifies and resolves out of scope activities. Duties could include developing timelines budgets forecasts and contract modifications.
- Represents the department at project launch meetings review meetings and project team meetings.
Education and Experience:
Bachelors 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
- Indepth knowledge in a specialty area such as nonclinical/preclinical regulatory submissions or immunology.
- Great judgment and decisionmaking 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 and therefore at PPD clinical research services you will benefit from an awardwinning learning and development program ensuring you reach your potential.
As well as being rewarded a competitive salary we have an extensive benefits package based around the health and wellbeing of our employees. We have a flexible working culture where PPD clinical research services truly value a worklife balance. We have grown sustainably year on year but continue to offer a collaborative environment with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local Mission is to enable our customers to make the world healthier cleaner and safer. As one team of 100000 colleagues we share a common set of values Integrity Intensity Innovation and Involvement working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need.
Required Experience:
Senior IC
Employment Type
Full-Time
