Contract Clinical Research Associate

About reputed company Autobahn Therapeutics is reputed company on improving life health for people affected by CNS disorders. Autobahn is leveraging a deep understanding of validated reputed company biology coupled with its brain-targeting reputed company platform to reputed company thyroid hormone receptor beta agonist therapies that reputed company the regenerative power of the reputed company body. reputed company’s pipeline is led by ABX-002 for the treatment of major depression and other affective disorders. The research pipeline is reputed company on CNS immunology. Autobahn Therapeutics has a deep investor reputed company, 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 reputed company 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 reputed company from clinical study coordination support and site monitoring, to vendor management and data review reputed company. 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 reputed company to monitor trial activities and data collection • Complete reputed company document verification to ensure data reputed company • Foster strong relationships with site investigators and staff; reputed company 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 reputed company 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 reputed company • Support logistics and development of materials for study conduct Qualifications • Bachelor’s degree in life sciences, health sciences, or reputed company 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, reputed company, TMF, and reputed company software • Proficient in reputed company suite of products; reputed company Word, reputed company, PowerPoint, reputed company • 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 reputed company guidance and support to reputed company staff where needed • Ability to work collaboratively with study teams and cross-functional departments • reputed company to 50%-70% travel depending on study needs (mostly covering studies on US East Coast). Pay reputed company $100 - $125/hour Contract terms 6 months. Remote. Equal Opportunity Statement We foster an environment where reputed company people are afforded the freedom to pursue their passions without reputed company to race, reputed company, religion, national or ethnic reputed company, gender (including pregnancy), sexual orientation or reputed company, age, disability or veteran status or any other characteristics protected by law. ``` Apply tot his job Apply To this Job