Clinical Research Associate II / Sr. CRA, Eastern or Central US

Rho Inc

1d•$90,000 - $140,000•Remote

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 to play an integral role in driving project success. In this remote position, you will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations, and Rho Standard Operating Procedures. You will conduct site visits to assess adherence to protocol and regulatory requirements, manage documentation, and ensure data remains audit-ready. This role requires proven monitoring skills and involves up to 80% travel, with 8-10 site visit days per month, and requires you to be located within a 1-hour commute of a US metropolitan airport.

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, 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 our collaborative culture with honesty and integrity with a willingness to learn and train. 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.

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