About the position Join Rho and redefine your career in clinical research. We are seeking a Clinical Research Associate II or Senior Clinical Research Associate with experience in monitoring pain studies to join our team. As a CRA II or Senior CRA, you will be integral to driving project success by performing and coordinating all aspects of the clinical monitoring and site management process. This includes conducting site visits to assess adherence to protocol and regulatory requirements, managing documentation, and ensuring data is audit-ready. This is a remote role, requiring travel for site visits. Rho offers a stable and collaborative environment where you can take risks, innovate, and develop a rewarding career. You'll work with talented individuals who are passionate about healing, curing, and solving health challenges. Our Clinical Monitoring team values the contentment, financial rewards, and career growth experienced at Rho.

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

Requirements

• BA/BS, preferably in a life science, nursing, pharmacy or related field
• Approximately 2 years (CRA II) or 4-5 years+ (Senior CRA) 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
• Committed to Quality: Attention to detail, deep understanding of high-quality scientific standards, 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 our collaborative culture with honesty and integrity with a willingness to learn and train. Value a strong team spirit highlighted by loyalty, accountability, and mutual trust.
• Critical Thinker: Evaluate situations and opportunities objectively and incisively; craft novel, practical solutions.
• Agile and Adaptable: Ability to change quickly. Eagerly anticipate, respond to, and take advantage of changes in our environment. Embrace risk but manage it by planning, accepting, and learning from both failures and successes.

Nice-to-haves

• Experience in monitoring pain studies

Benefits

• Medical insurance
• Vision insurance
• Dental insurance
• HSA
• FSA
• EAP
• Life insurance
• Disability insurance
• 401(k)
• Paid time off
• Holidays
• Parental leave
• Bereavement leave