Medical writerPPD

Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies. • May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs. • Ensures compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving optimal results. • May assist in program management activities. Duties could include assisting with developing timelines, budgets, forecasts for assigned deliverables. • Represents the department at project launch meetings, review meetings, and project team meetings.
Qualifications
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). Experience working in the pharmaceutical/CRO industry preferred Experience in scientific writing advantageous
Knowledge, Skills and Abilities:
Solid medical writing skills, including grammatical, editorial, and proofreading skills
Ability to interpret and present complex data accurately and concisely
Effective administrative, organizational and planning skills; attention to detail and quality
Ability to work on own initiative and effectively within a team
Effective oral and written communication skills
Good knowledge of regulatory documentation and drug development process
Great judgment and decision-making skills
Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook
PPD

Taguig City, Metro Manila
Permanent
Full-time