Clinical Research Associate II
**Clinical Research Associate II** **- Unblinded** **USA - Southeast** Why settle for one thing when you can have everything? Labcorp Drug Development gives you the best **two for one** opportunity for career growth. Who doesn't want twice the perks - working at one of the largest FSP CROs-and partnering with one sponsor with a dedicated therapeutic focus. Our Energizing Purpose, Exceptional People and Extraordinary Potential combined with collaborative and proactive teams offer a great place for you to continue honing your therapeutic skills and growing and excelling in new exciting research. Our reach is global - extending to 60+ countries making us one of the largest FSP CROs. So, no matter where you are located on the globe, we have an FSP opportunity for you. We are seeking an Unblinded Clinical Research Associate, a specialized role, which primarily focuses on drug accountability, at the site level, across a range of protocols and therapeutic areas. **Additional responsibilities include:** + Organize and make presentations at Investigator Meetings + Participate in the development of protocols and Case Report Forms as assigned + Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings, and other tasks as instructed by supervisor as assigned + Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned + Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management **Requirements:** + University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate + Minimum of at least 1 year of Onsite Clinical Monitoring experience along with at least 1 year total in clinical research experience is required + Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements + Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process + Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs + Good planning, organization and problem-solving abilities; Ability to work with minimal supervision + COVID-19 vaccination required + Valid Driver's License **Great Benefits at Labcorp:** Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: + Medical + Dental + Vision + Life, STD/LTD + 401(K) + ESPP + Paid time off (PTO) or Flexible time off (FTO) + Company bonus where applicable **Labcorp is proud to be an Equal Opportunity Employer:** As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement (https://www.labcorp.com/hipaa-privacy/web-privacy-policy) .