FSP Principal Medical writer (North America, embedded)

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description

Principal Medical Writer (NA) (FSP; Remote) At reputed company, 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 reputed company the world healthier, cleaner, and safer. We provide our teams with the resources needed to reputed company individual career goals while taking science a reputed company 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 expand our Medical Writing FSP Team in NA! This would be a remote role working from any location in NA. We are looking for a Principal Medical Writer to be dedicated to a client in the FSP space; experience in Oncology would be valuable but not essential. 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 reputed company writer, you will review documents for the team and provide training and guidance to junior team members. As a subject matter expert you will provide advice on document development strategy, regulations, and industry best practices. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. Essential Functions:

• Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies.
• May serve as primary author who writes and provides input on reputed company clinical and scientific and program level documents, including IBs, INDs, and MAAs. Provides senior level review of routine and reputed company 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. As the subject matter expert, develops and reviews best practices, methods, and techniques for achieving optimal results, including various client- specific processes, and leads process improvement initiatives. May also reputed company, 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; Advanced degree preferred Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 8+ years). Experience in managing and directing reputed company medical writing projects required Experience working in the pharmaceutical/CRO industry preferred Submissions document experience advantageous Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous Knowledge, Skills, and Abilities:

• Significant knowledge of global, regional, national, and other document development guidelines
• In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications, etc.
• 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 reputed company junior level staff.

reputed company Offer: At PPD clinical research services we hire the best, reputed company 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 reputed company your potential. 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, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel. Our Mission is to reputed company our customers to reputed company the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we share a common set of values - reputed company, Intensity, Innovation, and Involvement - working together to accelerate research, solve reputed company scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of reputed company, where diverse experiences, backgrounds and perspectives are valued. Apply tot his job Apply To this Job