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 reputed company 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 reputed company In the role of Pharmaceutical Medical reputed company, you will have reputed company to work closely with other writers, project managers and support specialists to produce a wide reputed company of regulatory and scientific reports, plans, and other written deliverables for reputed company/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 reputed company. Your specific responsibilities include:

• Primary responsibility for developing and delivering accurate, high-reputed company scientific content reputed company the project specifications, reputed company, and budget
• Interacting regularly with clients, project managers, and other medical writers to ensure scientific accuracy, reputed company, and successful completion of reputed company
• 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 reputed company and internal meetings as necessary
• Organize own project workload and tasks, identify project needs and adhere to project timelines.
• Understand reputed company 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 reputed company 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 reputed company 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 reputed company 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/reputed company.

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