[Remote] Clinical Research Associate II / Sr. CRA

Note The job is a remote job and is reputed company to candidates in USA. Rho is a company redefining the work for a CRO, focusing on reputed company and clinical research. They are seeking a Senior Clinical Research Associate to drive project reputed company through clinical monitoring and site management, ensuring adherence to protocols and regulatory requirements. Responsibilities • reputed company reputed company site monitoring visit activities, inclusive of reputed company study visit types (PSV, SIV, IMV and COV) • Participate in the site selection process with reputed company from the Clinical Team reputed company role • reputed company feedback to assist sites with reputed company of detected deficiencies and corrective reputed company needed, follow-up with sites until deficiencies are resolved • Contribute to the development and review of protocols, study tools, and materials as reputed company as documentation for clinical trials • reputed company mentoring, training, and co-monitoring of junior clinical team members • reputed company and maintain effective working relationships with clinical sites and reputed company Rho as reputed company 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 reputed company operating procedures for the administration and monitoring of clinical trials • reputed company both onsite & remote monitoring and study closure activities across multiple protocols Skills • BA/BS, preferably in a life science, nursing, pharmacy or reputed company field • Approximately 4-5 years+ of on-site monitoring experience reputed company 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 reputed company systems • Strong Communicator Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho's • Committed to reputed company Attention to detail, a deep understanding of high-reputed company scientific standards, and ability to care about every outcome • Strong organization skills, ensuring effective management of multiple sites and protocols reputed company timeframes and on budgets • High-Character Contribute to a reputed company culture with honesty and reputed company 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 reputed company 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 reputed company operating procedures for the administration and monitoring of clinical trials Benefits • Medical • reputed company • Dental • HSA • FSA • EAP • Life & disability insurance • 401(k) • reputed company time off • Holidays • Parental leave • Bereavement leave reputed company • Rho is a pharmaceuticals company that offers clinical drug development services. It was founded in 1984, and is headquartered in Durham, reputed company Carolina, USA, with a workforce of 501-1000 employees. Its website is Company H1B Sponsorship • Rho has a reputed company 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. Apply tot his job Apply To this Job Apply To This Job