[Remote] Clinical Research Associate II / Sr. CRA

Note: The job is a remote job and is open to candidates in USA. Rho is a company redefining the work for a CRO, focusing on healthcare and clinical research. They are seeking a Senior Clinical Research Associate to drive project success through clinical monitoring and site management, ensuring adherence to protocols and regulatory requirements. Responsibilities • Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV) • Participate in the site selection process with oversight from the Clinical Team Lead role • Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved • Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials • Provide mentoring, training, and co-monitoring of junior clinical team members • Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements • Attend and present at meetings and conferences, including Investigator Meetings • Participate in the RFP process, including business development meetings • Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials • Perform both onsite & remote monitoring and study closure activities across multiple protocols Skills • BA/BS, preferably in a life science, nursing, pharmacy or related field • Approximately 4-5 years+ of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology required for comprehension and execution of clinical protocol • Computer literacy, including proficiency in MS Office and use of EDC systems • Strong Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho's • Committed to Quality: Attention to detail, a deep understanding of high-quality scientific standards, and ability to care about every outcome • Strong organization skills, ensuring effective management of multiple sites and protocols within timeframes and on budgets • High-Character: Contribute to a collaborative culture with honesty and integrity with a willingness to learn and train • Critical Thinker: Ability to evaluate situations and opportunities objectively and craft novel, practical solutions • Agile and Adaptable: Ability to change quickly and embrace risk while managing it • Experience in Psychiatry (preferably MDD) • Experience in mentoring, training, and co-monitoring junior clinical team members • Experience in participating in the RFP process, including business development meetings • Experience in contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials Benefits • Medical • Vision • Dental • HSA • FSA • EAP • Life & disability insurance • 401(k) • Paid time off • Holidays • Parental leave • Bereavement leave Company Overview • Rho is a pharmaceuticals company that offers clinical drug development services. It was founded in 1984, and is headquartered in Durham, North Carolina, USA, with a workforce of 501-1000 employees. Its website is http://rhoworld.com. Company H1B Sponsorship • Rho has a track record of offering H1B sponsorships, with 1 in 2025, 1 in 2024, 4 in 2023, 1 in 2022, 1 in 2021. Please note that this does not guarantee sponsorship for this specific role.