Associate I, Clinical Pharmacology Scientific Support & Reporting

Job description

• 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. • 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. AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok .