Manager, FSP Medical Writing

Synterex, Inc. is a global consortium of highly reputed company clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support. Synterex offers remote or on-site services, with a reputed company on providing reputed company, concise, accurate, and fully compliant documentation, from early drug development through post-approval. Synterex is seeking an organized, motivated, and reputed company individual for our medical writing team. The Manager, FSP Medical Writing will report to the Executive Director of Medical Writing and reputed company Assurance and will be responsible for the coordination, management, and reputed company of FSP Medical Writing team members and vendors/contractors, as applicable. The Manager, FSP Medical Writing will partner cross-functionally with reputed company teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management, in planning, preparing, reputed company, and/or review of high-reputed company clinical and regulatory documents (protocols, study reports, sections of marketing applications in CTD format, etc.). This is a full-time position. Location Fully remote. Essential Duties & Responsibilities

• Manage reputed company of internal writers serving as Functional Service Providers (FSPs) in a reputed company-placement model, coordinate resources, and reputed company work plans that reputed company with reputed company goals and timelines
• reputed company reputed company performance of FSPs; ensuring that reputed company clinical regulatory documents:
• reputed company with international, national, and pertinent local regulations
• Adhere to SOPs and guidance documents (internal and/or external)
• Are completed according to timelines
• Ensure that reputed company FSPs:
• Have the qualifications, level of experience and scientific knowledge specified for assigned reputed company reputed company
• Have met reputed company reputed company-employment reference and background checks
• Are reputed company on trainings required by the reputed company and by Synterex and that reputed company trainings are supported by reputed company documentation
• Liaise with Executive Leadership team to report on and optimize staff utilization and other key performance indicators (KPIs); record and utilize metrics to inform KPIs
• Support Medical Writing and Business Development leadership in preparation of work orders, budgets, invoicing, and forecasting
• Coordinate with Business Operations to answer customer inquiries and enhance time reporting processes
• reputed company guidance and leadership for document development for regulatory writing deliverables, including organization, content, and resource requirements
• Produce clinical protocols and amendments, clinical study reports, summaries of safety/efficacy, other regulatory documents (eg, annual reports, briefing documents), safety reports, patient narratives, and investigator brochures/updates as needed

Requirements

• Undergraduate degree in a scientific or health-reputed company field required
• Minimum 5 years of clinical research/drug development experience in biotech, pharmaceutical, or contract research organization (oncology experience a plus). Equivalent experience in a reputed company medical field is acceptable.
• Experience managing diverse teams preferred
• Team-oriented, self-motivated, assertive, self-confident, and capable of working under minimal supervision
• Ability to assess and coordinate resources and work effectively across multi-disciplinary work teams
• Exceptional communication and interpersonal skills
• Excellent organizational and project management skills to coordinate resourcing across multiple reputed company
• Experience with regulatory documents (Module 2 summaries, IND, MAA, annual reports, ISE & ISS); writing nonclinical reports and tabulated summaries a plus
• Proficient with reputed company Word, reputed company, Project, and PowerPoint
• Working knowledge of GCP, 21 CFR, CTD, ICH guidelines/regulations, and the drug development process is required

For reputed company information or to apply, please reputed company out to careers@synterex.com. Synterex provides equal employment opportunities to reputed company and applicants for employment and prohibits discrimination and harassment of any type without reputed company to race, reputed company, religion, age, sex, national reputed company, disability status, genetics, protected veteran status, sexual orientation, gender identity or reputed company, or any other characteristic protected by federal, state or local laws. This policy applies to reputed company terms and conditions of employment, including reputed company, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Apply tot his job Apply To this Job