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Clinical Research Associate II / Sr. CRA

3 weeks ago
United States
Full-time
Senior
Project Manager
Project and Program Management
Apply Now
Rho

Rho

Rho is a full-service Contract Research Organization (CRO) that combines innovation and scientific rigor to maximize results in every phase of clinical research. With a global team of experts, Rho ensures consistent and efficient trials, offering compr...

Biotechnology
251-1K
Founded 1984
View All Jobs 16

Description

  • Perform site monitoring visit activities across all study visit types, including PSV, SIV, IMV, and COV.
  • Conduct both onsite and remote monitoring and study closure activities across multiple protocols.
  • Participate in the site selection process with oversight from the Clinical Team Lead.
  • Identify site deficiencies, provide corrective-action feedback, and follow up until issues are resolved.
  • Contribute to the development and review of protocols, study tools, materials, and clinical trial documentation.
  • Mentor, train, and co-monitor junior clinical team members.
  • Develop and maintain effective working relationships with clinical sites and internal Rho teams.
  • Ensure communication of project goals and critical requirements to study stakeholders.
  • Attend and present at meetings and conferences, including Investigator Meetings.
  • Participate in the RFP process, including business development meetings, and support internal clinical operations initiatives and SOPs.

Requirements

  • BA/BS degree, preferably in a life science, nursing, pharmacy, or related field.
  • Approximately 4-5+ years of on-site monitoring experience in the CRO, pharmaceutical, or biotechnology industry.
  • Demonstrated understanding of medical and therapeutic area knowledge and medical terminology.
  • Proven monitoring skills and experience assessing site adherence to protocol and regulatory requirements.
  • Ability to manage required documentation and maintain audit-ready data.
  • Computer literacy, including proficiency in MS Office and EDC systems.
  • Strong written, verbal, and presentation communication skills.
  • Strong organization skills and ability to manage multiple sites and protocols within timelines and budgets.
  • Willingness to work remotely within 1 hour of a US metropolitan airport and travel 8-10 site visit days per month, up to 80% travel.
  • Preferred psychiatry experience, preferably in major depressive disorder (MDD).

Benefits

  • Comprehensive medical, vision, dental, HSA, FSA, EAP, life, disability, and 401(k) benefits.
  • Paid time off, holidays, parental leave, and bereavement leave.
  • Flexible work-life balance support.
  • Remote role with travel-based fieldwork.
  • Starting compensation range of $90,000 to $145,000 per year.

Interested in this position?

Apply directly on the company website

Apply Now

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