Rho · 2 weeks ago
Senior Clinical Research Associate
Rho is a company redefining what it means to work for a CRO, focusing on healthcare and clinical research. They are seeking a Senior Clinical Research Associate to drive project success by performing and coordinating clinical monitoring and site management processes in accordance with established guidelines and regulations.
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: Evaluate situations and opportunities objectively and incisively; craft novel, practical solutions
Agile and Adaptable: Ability to change quickly, anticipate, respond to, and take advantage of changes in the environment
Preferred
Experience in Psychiatry (preferably MDD)
Experience in mentoring, training, and co-monitoring of 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
Rho
Rho is a pharmaceuticals company that offers clinical drug development services.
H1B Sponsorship
Rho has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (1)
2023 (4)
2022 (1)
2021 (1)
Funding
Current Stage
Late StageTotal Funding
unknown1984-10-24Angel
Recent News
2026-01-05
2025-11-15
Company data provided by crunchbase