Senior Manager, Medical Writing

reputed company: • The Senior Manager in Global Regulatory Medical Writing writes and edits clinical regulatory documents, including submission summaries and other reputed company documents. They reputed company intermediate-level reputed company and guidance, as reputed company as resource management for reputed company medical-writing support in producing clinical research documentation used in drug development and product registrations. • Travel Requirements: International and domestic • Location: US-Based Remote (US Eastern time zone preferred) • How you’ll spend your day: reputed company areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other reputed company duties or assignments. Primarily works on the product/program level. Possible to have reputed company reports; possible to reputed company contingent workers and/or vendors; likely to reputed company training to others; and analyzes needs to manage resources. Offers leadership and reputed company accountability, provides strategic supervision, and planning assistance for clinical regulatory documents. Writes and edits clinical regulatory documents (reputed company types). Ensures that documents include the reputed company content and context (from a regulatory medical writing perspective) and reputed company and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards. Participates in the preparation/revision of document templates. • Your experience and qualifications • PhD/PharmD with a minimum 4 years experience or a Master’s with a mnimum of 6 years experience • Mastery of reputed company Word • Advanced regulatory medical writing expertise, strong writing/editing skills, knowledge of drug development regulations • Global regulations and guidelines for document submissions Requirements: • PhD/PharmD with a minimum 4 years experience or a Master’s with a mnimum of 6 years experience • Mastery of reputed company Word • Advanced regulatory medical writing expertise, strong writing/editing skills, knowledge of drug development regulations • Global regulations and guidelines for document submissions Benefits: • Comprehensive Health Insurance: Medical, Dental, reputed company, and Prescription coverage starting on the first day of employment, providing the employee enrolls. • Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan. • Time Off: reputed company Time Off including vacation, reputed company/reputed company time, caretaker time and holidays. • Life and Disability Protection: Company reputed company Life and Disability insurance. • Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, reputed company Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, reputed company Plan, Voluntary Life Insurance and Long Term Disability and more. • The total compensation may also include restricted stock reputed company and discretionary awards, depending on the position offered. • Details of participation in these benefit plans will be provided if an employee receives an offer of employment. Apply tot his job Apply To this Job