Associate I, Clinical Pharmacology Scientific Support & Reporting

About the role

Prepare scientific reports and presentations related to clinical trials using available software and templates. Assist in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.

Responsibilities

• 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

• Bachelors degree in Science related to Field with +2 years experience in pharmaceutical industry
• 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