job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you!
location: North Chicago, Illinois
job type: Contract
salary: $38.00 - 42.11 per hour
work hours: 8 to 4
- Responsible for ensuring the quality of clinical regulatory documents by conducting quality control (QC) review utilizing checklists for all applicable documents, uploading QC review documentation to the Trial Master File (TMF), and, ensuring QC review documentation from all applicable functional areas is completed and uploaded to the TMF per the established business processes and procedures.
- Must be familiar with ICH and GCP Guidelines.
- Must demonstrate good interpersonal and organizational communication skills.
- Determines scope of QC review with the document author and the source documents and/or data required (in addition to utilizing any applicable checklist).
- Conducts independent quality review of documents by checking against source (documents and/or data) to ensure that the results presented are accurate (emphasis on checking the numbers/data in the text and in-text tables against the final statistical tables, listings, and graphs (TLGs).
- Deliver documented quality review comments/checklist to document author..
- Ensures QC review documentation from all applicable functional areas is complete and uploaded to the TMF per the established business processes and procedures.
- Maintains strong knowledge of clinical regulatory documents requiring QC as well as business processes and procedures for these documents. Demonstrates strong attention to detail and a high level of quality, consistency, and accuracy in work effort.
- Accountable for meeting the main objectives of the assigned projects/roles and responsibilities within established timelines and with an appropriate quality level.
- Drives the QC of clinical regulatory documents to timely completion.
- Accountable to Senior Manager, Medical Writing. Exhibits a moderate level of technical competency and requires a low level of counsel and guidance.
- Mentors and provides guidance/training to less senior MW QC staff as applicable.
- Expedient escalation of issues to management is essential and may have a direct impact on the ability to meet project timelines.
- Daily interaction with Medical Writers and/or Medical Writing managers as well as interface/communication with applicable cross-functional areas.
- Communicates and provides deliverables to Medical Writers, Medical Writing managers, and others as applicable.
- Bachelor's degree (BA/BS) required.
- 2-4 years relevant pharmaceutical industry experience in medical writing, clinical research, quality, or related area such as regulatory or product support.
- Experience in quality review of clinical regulatory documents (i.e. Clinical Study Report, Investigator Brochure, Protocols, etc.).
- Experience being flexible with changing workload that requires prioritization and planning to support immediate/urgent business needs.
- Proficient experience in use of MS Office (e.g., Word, Excel, Outlook, PowerPoint) and Adobe Acrobat.
skills: Quality control, MS-WORD, MS-EXCEL, MS-Powerpoint, GCP (Good Clinical Practice), ICH Regulations, TMF
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.