Contract Clinical Research Associate
About the Company Autobahn Therapeutics is focused on improving life health for people affected by CNS disorders. Autobahn is leveraging a deep understanding of validated human biology coupled with its brain-targeting chemistry platform to develop thyroid hormone receptor beta agonist therapies that harness the regenerative power of the human body. The company’s pipeline is led by ABX-002 for the treatment of major depression and other affective disorders. The research pipeline is focused on CNS immunology. Autobahn Therapeutics has a deep investor base, anchored by ARCH Venture Partners, and is located in San Diego, CA. For more information, visit www.autobahntx.com. About the Role The Contract Clinical Research Associate (CRA) is primarily responsible for the monitoring and oversight of site activities associated with the management of clinical studies under the direction of, or as delegated by a member of the Global Clinical Operations team. Responsibilities will range from clinical study coordination support and site monitoring, to vendor management and data review projects. This position will report to the Sr. Manager of Clinical Operations is estimated to be a contract length of 6 months. Responsibilities • Monitor study sites and activities to ensure adherence to protocols, Good Clinical Practices (GCP), and applicable regulatory requirements • Conduct regular site visits to monitor trial activities and data collection • Complete source document verification to ensure data integrity • Foster strong relationships with site investigators and staff; provide training to site staff on the study protocol and best practices as needed • Review and analyze clinical trial data listings for accuracy and completeness • Assist the clinical operations team with vendor and site management • Implement accurate tracking systems, forms, and other relevant documents to support clinical studies • Assist in the preparation of spreadsheets, presentations, etc. utilizing Microsoft Office Suite • Assist in the periodic review and QC of eTMFs to support inspection readiness and archiving of completed studies • Maintain electronic files of clinical trial documents for ongoing projects • Support logistics and development of materials for study conduct Qualifications • Bachelor’s degree in life sciences, health sciences, or related field • 2+ years’ experience as a Clinical Research Associate (experience in CNS preferred) Required Skills • Understanding of Good Clinical Practices (GCP) • Strong written and verbal communication skills • Experience utilizing CTMS, EDC, TMF, and related software • Proficient in Microsoft suite of products; Microsoft Word, Excel, PowerPoint, Outlook • Strong attention to detail, and excellent organizational and prioritization skills • Motivated to work in a fast-paced, high-accountability environment • Ability to problem solve and provide guidance and support to professional staff where needed • Ability to work collaboratively with study teams and cross-functional departments • Open to 50%-70% travel depending on study needs (mostly covering studies on US East Coast). Pay range $100 - $125/hour Contract terms 6 months. Remote. Equal Opportunity Statement We foster an environment where all people are afforded the freedom to pursue their passions without regard to race, color, religion, national or ethnic origin, gender (including pregnancy), sexual orientation or expression, age, disability or veteran status or any other characteristics protected by law. ``` Apply tot his job