Associate I, Clinical Pharmacology Scientific Support & Reporting
AbbVie
5 months ago
Remote friendly (North Chicago, IL)
United States
Clinical Research and Development
Responsibilities:
- Prepare scientific reports and presentations related to clinical trials using available software and templates.
- Assist in constructing Phase 1 clinical study planning documents and write Phase 1 protocols.
- Comply with procedures in relevant IQS documents and study protocols.
- Comply with management directives regarding clinical studies.
- Perform literature and competitive intelligence searches.
- Analyze clinical study data using available software, including ongoing blinded/unblinded pharmacokinetic analysis.
- Receive and complete assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.
Qualifications:
- Bachelor’s degree in Science related field with +2 years’ experience in the pharmaceutical industry; or Master’s degree in pharmacology or related field.
- Associate degree or RN with 6+ years’ experience in the pharmaceutical industry may be additionally considered.
- Good oral and written communication skills.
- Ability to use computer tools 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.
Benefits (if explicitly stated):
- Paid time off (vacation, holidays, sick); medical/dental/vision insurance; 401(k) to eligible employees.
- Eligible to participate in short-term incentive programs.
- Prepare scientific reports and presentations related to clinical trials using available software and templates.
- Assist in constructing Phase 1 clinical study planning documents and write Phase 1 protocols.
- Comply with procedures in relevant IQS documents and study protocols.
- Comply with management directives regarding clinical studies.
- Perform literature and competitive intelligence searches.
- Analyze clinical study data using available software, including ongoing blinded/unblinded pharmacokinetic analysis.
- Receive and complete assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.
Qualifications:
- Bachelor’s degree in Science related field with +2 years’ experience in the pharmaceutical industry; or Master’s degree in pharmacology or related field.
- Associate degree or RN with 6+ years’ experience in the pharmaceutical industry may be additionally considered.
- Good oral and written communication skills.
- Ability to use computer tools 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.
Benefits (if explicitly stated):
- Paid time off (vacation, holidays, sick); medical/dental/vision insurance; 401(k) to eligible employees.
- Eligible to participate in short-term incentive programs.