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Medical Reviewer/Safety Reviewer
Company | Intellectt Inc |
Address | Columbus, OH, United States |
Employment type | CONTRACTOR |
Salary | |
Category | Medical Equipment Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-08-23 |
Posted at | 10 months ago |
Role: Medical Reviewer/Safety Reviewer - A
Location: Columbus, OH - 43219
Duration: 11 Months on W2 (Possibility of contract extension).
Shift Timings: 8 AM to 5 PM
Skills Looking For:
- Do daily case processing for clinical studies.
- Need to get into various computerized systems.
- Use their medical background and judgment to interpret lay terms to medical terms. For example ear infection. The medical terminology for this disease is Otitis media. This candidate must have a strong understanding of medical terminology as this is what they will do in a coding online dictionary.
- Will do some follow-ups either with the clinical study team or clinical study site if the doctors and researchers conducting the study. If there was any confusion or any adverse situations reported. They will do this within the electronic system for audit purposes or via emails.
- Good documentation practices are required because they will keep those emails in a document fashion.
- Be part of team meetings for clinical studies and give reports to the team on various things that are being reported and alert the managers by raising issues that are concerning and providing them with some feedback and guidance.
- Will do a lot of Medical writing. For instance paragraph writing for a specific case that might come in. Do an assessment on that and summarize what is being told to Abbott and at the end of the study, they will need to write a summary of all of the data that came in for that study.
- Writing experience: Editor
- Some Math and Statistics background.
- Any clinical monitoring experience: clinical study monitor at clinical site/clinical research coordinator experience.
- Backfill role; Experience of the previous candidate: Registered dietician degree, good editorial experience, and showed willingness to learn.
- Any hospital experience; Nurse background (have written summary of patient history); a narrative of a medical case.
- Biology degree with clinical research writing exp will also be a good fit.
- Will work on ETMS.
- Work with case report form developers but not actually develop case report forms on their own.
- Food Science and Nutrition degree will also be fine.
- Open to Public health background as well as they will have data analysis experience and it will be helpful for them to make summaries at the end of the clinical study. They will need a little more training but if they are willing to learn, then it is doable.
- This is more entry-level and someone with a lot of experience will not be comfortable doing simple tasks like processing case studies or writing medical case studies. Refrain from submitting individuals with more experience.
Education and Experience:
- Bachelor's degree is highly preferred (Science degree)
- Open to Associate's degree in Health care or Science.
- 0 to 3 years’ experience (Open to fresh graduates if they have appropriate scientific background).
- Master's degree will be overqualified for this role.
Top Skills:
- Strong medical knowledge (Medical terminology).
- Some writing experience.
- Clinical Coordinator/Clinical monitoring exp.
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