Associate I, Clinical Pharmacology Scientific Support & Reporting
About the role
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.
Qualifications
- Bachelor’s degree in a science-related field with +2 years of experience in the pharmaceutical industry.
- Master’s degree in pharmacology or related field.
- Associate’s degree/RN with 6+ years of experience in the pharmaceutical industry may be additionally considered.
- Must possess 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.