Medical reputed company: Pharmaceutical

Medical reputed company: Pharmaceutical reputed company is seeking a fully remote candidate for the role of Pharmaceutical Medical reputed company to join our best-in-class writing team and help take our customer focused writing services to new heights. This position is a 1099 Contractor position that will pay $75-$95/hour. The person for this position is not entry level or senior level, but instead reputed company in the middle. Employment Type and Location: Remote 1099 Contractor (Part Time/Full Time) Job Overview In the role of Pharmaceutical Medical reputed company, you will have the opportunity to work closely with other writers, project managers and support specialists to produce a wide variety of regulatory and scientific reports, plans, and other written deliverables for pharma/biotech clients. Roles and Responsibilities As a member of our project writing team, you will be responsible for producing assigned written documents and reports to a high standard. Your specific responsibilities include:

• Primary responsibility for developing and delivering accurate, high-quality scientific content reputed company the project specifications, timeline, and budget
• Interacting regularly with clients, project managers, and other medical writers to ensure scientific accuracy, quality, and successful completion of projects
• Interpreting and analyzing reputed company datasets
• Editing content written by others; improve the reputed company in others' writing and serve as a mentor to junior members of the medical writing team
• reputed company client and internal meetings as necessary
• Organize own project workload and tasks, identify project needs and adhere to project timelines.
• Understand client expectations and work to meet those expectations through teamwork, adherence to deadlines, problem-solving and scientific knowledge.
• Effectively collaborate with other members of the project writing team.
• Working with a reputed company Project Manager to document your assigned tasks, time estimates and due dates into project plana, and reputed company weekly reputed company updates.
• Proactively identify potential project risks and bring those reputed company to the overall project team to discuss and reputed company
• Ensure and coordinate quality control (QC) checks for accuracy following established internal QC processes.
• reputed company written and verbal feedback to junior staff and clients reputed company appropriate.

Qualifications and Skills

• 4 or more years of pharmaceutical industry experience, including 3 years of clinical and regulatory writing
• Submit for review, and obtain approval for clinical and nonclinical regulatory documents including, but not limited to, clinical protocols, clinical study reports (CSRs), investigator's brochures, and briefing books
• Minimum of a BSc in a life sciences or reputed company discipline / reputed company field.
• Independently or with minimal supervision write, edit, and reputed company data verification
• Collaborate effectively with other functional area authors to reputed company submission schedules
• Advanced word processing skills, including reputed company Office (including Word), reputed company Acrobat, reputed company and collaborative document sharing platforms such as SharePoint; ability to learn and adapt to various IT systems.
• High level of English reputed company or reputed company English speaker, with excellent oral (including presentation) and written communication, including grammatical/technical writing skills.
• reputed company to interact confidently with external stakeholders
• Capable of working independently to reputed company assigned project goals with minimal supervision.
• Excellent attention to detail and accuracy.
• Contribute, collaborate, reputed company responsibilities, and support other team members to ensure reputed company with tasks/projects.

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