We're looking for a Clinical Studies Specialist III, working in the Pharmaceuticals & Medical Products industry in North Chicago, Illinois, United States.
Monitors and reports issues that require escalation to the appropriate Senior Manager and Director of the corresponding project for immediate resolution.
Assists with writing, compiling and distributing meeting notes, as requested.
Supports clinical study teams in their conduct of Phase I-IV studies according to Federal Regulations and ICH guidelines.
Provides project management support to the Recruitment and Retention team, and Trial Access and Awareness team.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
BS/BA degree, RN, BSN or equivalent
5+ years professional work experience in clinical research, pharmaceutical or health care industry preferred
High proficiency with Microsoft Office 365 (Word, PowerPoint, Excel, Outlook, OneNote) and ability to learn new computer systems easily
Work experience in clinical research, healthcare, pharmaceuticals, medical devices or equivalent that includes knowledge of GCP, CFR, handling of confidential information, importance of careful communication, etc.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.