Regulatory QC Document Reviewer Job at Rangam Consultants Inc.
Remote
Initially 3 months, with 6-month renewals
8 hours a day, core business hours 9-3 CST
- Prepares technical documents to support both domestic and international regulatory submissions.
- Incorporates text, graphs, charts, tables and statistical analysis.
- Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. 3-5 years exp.
- Requires a Clinical Background
What are the top 5 skills/requirements this person is required have?
- Experience in QC of regulatory clinical documents (Investigator Brochures, Clinical
- Study Reports, Protocols, etc.)
- Attention to Detail
- Ability to manage competing priorities
- Work in a team environment
- Strong communication skills
What years of experience, education, and/or certification is required?
- Bachelor’s degree required. 2-3 years relevant experience in QC of clinical regulatory
- documents or related experience.
What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
- Bachelor’s degree in science preferred.
What is the environment that this person will be working in (i.e. group setting vs individual role)?
- Independent and working as a team.
What positions/background experience do you feel are successful in this role
Authoring of regulatory clinical documents (Investigator Brochures, Clinical Study
Reports, Protocols, etc.) and/or QA auditing positions
Job Type: Contract
Salary: $13.48 - $50.00 per hour
Benefits:
- Flexible schedule
Schedule:
- 8 hour shift
Education:
- Bachelor's (Preferred)
Experience:
- regulatory documentation: 3 years (Preferred)
- QC review of regulatory documents: 3 years (Preferred)
- quality documentation: 3 years (Preferred)
Work Location: Remote
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