Associate Clinical Team Lead

17 hours, 29 minutes ago
Full-time
Mid Level
Project and Program Management
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

Description

  • Support CTLs with end-to-end clinical execution, ensuring adherence to protocols, timelines, and regulations.
  • Track recruitment, study metrics, monitoring activities, and documentation.
  • Support clinical operations timelines, resourcing, budgets, and activity tracking.
  • Identify clinical risks and contribute to corrective actions and mitigation strategies.
  • Coordinate communication among clients, sites, CRAs, and internal cross-functional teams.
  • Assist with CRA and IHCRA onboarding, training, performance feedback, and team development.
  • Support protocol deviation review, reconciliation, and related cross-functional coordination.
  • Assist with study protocol and document development, including monitoring plans and case report forms.
  • Support planning and execution of risk-based Quality Compliance Visits.
  • Monitor regulatory and industry developments affecting clinical research operations.

Requirements

  • Bachelor’s degree, preferably in life science, nursing, pharmacy, or a related field.
  • At least 3 years of clinical research experience in a CRO, pharmaceutical, or biotechnology setting.
  • At least 2 years of on-site monitoring experience.
  • Leadership experience managing or leading teams in a CRO or pharmaceutical environment.
  • Strong knowledge of GCP, regulatory requirements, clinical trial processes, and documentation.
  • Excellent interpersonal and communication skills for building client and team relationships.
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Proactive, solutions-oriented approach with the ability to make decisions and lead initiatives.
  • Experience with clinical trial management software and EDC systems.
  • Fluency in written English for CV submission.

Benefits

  • Permanent remote role with occasional travel for site visits and client meetings.
  • Work-life balance and flexibility to support personal commitments.
  • Stable company environment with opportunities for long-term career development.

Interested in this position?

Apply directly on the company website

Apply Now

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