Associate I, Clinical Pharmacology Scientific Support & Reporting

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 and support ongoing blinded/un-blinded pharmacokinetic analysis using available software.
- Receive and complete assignments/tasks from Scientific Staff or Therapeutic Area MD within a given time period with supervision.
- Produce high-quality work and pay close attention to detail.

Qualifications:
- Bachelor’s degree in a Science-related field with 2+ years’ pharmaceutical industry experience; or Master’s degree in pharmacology or related field.
- Associate’s degree/RN with 6+ years’ pharmaceutical industry experience may be considered.
- Good oral and written communication skills.
- Ability to use a 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.