Associate I, Clinical Pharmacology Scientific Support & Reporting
AbbVie•North Chicago, IL
•$65,500 - $125,500
About The Position
To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.
Requirements
- Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical industry. Or Masters degree in pharmacology or related field.
- Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered.
- Must possess good oral and written communication skills
- Ability to use computer to generate reports, analyze data, and create presentations
- Previous experience may be narrowly-focused or limited.
- Ability to identify opportunities and participate in process improvement initiatives.
Responsibilities
- Prepare scientific reports and presentations related to clinical trials using available software and templates.
- Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
- Comply with procedures set forth in relevant IQS documents and Study protocols
- Comply with the directives issued by the management regarding clinical studies.
- Commit to producing work of the highest quality
- Pay close attention to detail
- Perform literature and competitive intelligence searches
- Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis
- Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.
Benefits
- paid time off (vacation, holidays, sick)
- medical/dental/vision insurance
- 401(k)
- short-term incentive programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
