Rho · 18 hours ago
Senior Clinical Research Associate (West Coast)
Rho is a company redefining the work environment for CROs, emphasizing a collaborative and innovative culture. They are seeking a Senior Clinical Research Associate to drive project success through clinical monitoring and site management, ensuring compliance with regulations and quality standards.
BiotechnologyHealth CarePharmaceutical
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
Qualification
Required
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
Preferred
Experience in Psychiatry (preferably MDD)
Experience with site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
Experience in the site selection process with oversight from the Clinical Team Lead role
Experience providing feedback to assist sites with resolution of detected deficiencies and corrective action needed
Experience contributing to the development and review of protocols, study tools, and materials as well as documentation for clinical trials
Experience mentoring, training, and co-monitoring of junior clinical team members
Experience developing and maintaining effective working relationships with clinical sites and within Rho
Experience attending and presenting at meetings and conferences, including Investigator Meetings
Experience participating in the RFP process, including business development meetings
Experience participating in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials
Experience performing both onsite & remote monitoring and study closure activities across multiple protocols
Benefits
Medical
Vision
Dental
HSA
FSA
EAP
Life & disability insurance
401(k)
Paid time off
Holidays
Parental leave
Bereavement leave
Company
Rho
Rho is a pharmaceuticals company that offers clinical drug development services.
Funding
Current Stage
Late StageTotal Funding
unknown1984-10-24Angel
Recent News
2026-01-05
2025-11-15
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