Remote Position (Preferably in the Eastern time zone) ***MUST BE BASED IN THE US***

JOB DESCRIPTION:

• Reviewing, revising, organizing, planning, summarizing, editing, and proofreading Clinical and Clinical Quality procedures, work instructions, forms, and templates.
• Working with Clinical Quality Assurance to provide detailed feedback on the review.
• Bringing clarity and consistency to documents through accurate and concise writing and effective use of document format.
• Potential to Interface cross-functionally within the Clinical and Clinical Quality Assurance team to edit documents and develop compliant processes and procedures.
• Organize findings from the review of procedures, work instructions, forms, and/or templates.
• Clearly and correctly state and summarize findings from review and conclusions in documents. Make suggestions or corrections to make procedures and work instructions clearer and more concise.
• Managing, organizing, and communicating project information and project activities.
• Advanced knowledge of Microsoft Word, Microsoft Excel, and PowerPoint.

MINIMUM QUALIFICATIONS:

• 5-8 years of Pharmaceutical Clinical Research and Trial experience.
• Previous Pharmaceutical Clinical Research and Trial audit and/or monitoring experience is required.
• Strong communication skills (verbal & written).

PREFERRED QUALIFICATIONS:

• Prior Pharmaceutical and medical device industry experience.
• Adaptable and effective collaborator in a team environment or in self-directed work.
• Self-motivated

REQUIRED QUALIFICATIONS:

• The candidates are required to be based in the US and it is preferred to have the candidates in the Eastern time zone.

LOCATION: Remote (preferably in Eastern time zone) **\ must be based in the US****

POSITION: 4 – 6 weeks assignment

SALARY: $90.00 - $100.00 Hourly

Job Type: Full-time

Pay: $90.00 - $100.00 per year