Senior Quality Control Reviewer United States Remote (Project-Based)
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Job Location:
Canton, OH - USA
Monthly Salary:
Not Disclosed
Posted on:
17 hours ago
Vacancies:
1 Vacancy
Department:
Job Summary
Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is a award-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical biotech and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit follow MMS on LinkedIn.
This is a project-based opportunity and not full time employment.
Senior Quality Control Reviewer
Job Specific Skills:
- Proficient with templates toolbars and macros
- Able to adapt to differentclient styleguides and document formatting requirements
- Proficient with correcting grammar & spelling errors with ensuring intra- and inter-document consistency
- Proficient withensuring scientificsenseand the correctness ofdata interpretation
- Proficient withthe QC of a wide range of regulatory documents including
- Investigators Brochure
- Protocols protocol amendments and summaries of changes
- ICFs and ICF amendments
- CSRs (synoptic abbreviated interim full addendum)
- Briefing Documents and Meeting Requests
- Assessment Aids
- Health Authority Responses
- CTD clinical modules (especially strong experience with 2.7.1 2.7.2 ISI)
- Additionally proficient withthe QC of a wide range of med comms documents would be advantageous but not necessary including
- Slide Decks
- Posters
- Abstracts
- Manuscripts
Job Requirements:
- College graduate in a scientific medical clinical discipline or related fieldis preferredbutrelevant QCexperienceis acceptable
- Minimum of 5 years experience in Quality Control or similar field required.
- Proficiency with MSWord and Excel.
- Clear and timelycommunication ableto work with others to clearly understand needs and solve problems.
- Basic understanding of CROs and scientific & clinical data/terminology & the drug development process.
Should you not have received a response within 14 days of your application please consider your application unsuccessful.
Required Experience:
Senior IC
Key Skills
- Facilities Management
- Banking
- Content Writing
- Customer Support
- Fun
- Airlines
About Company
MMS Holdings is a leading global data-focused CRO (Clinical research organization) & technology enabled clinical research and health data analytics solution company that supports the pharmaceutical, biotech, and medical device industries.
