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Clinical Team Lead

3 weeks ago
Spain, United Kingdom, Italy, Latvia, Poland
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

  • Manage end-to-end clinical execution for projects of moderate complexity, or support senior CTLs on larger or more complex projects.
  • Oversee recruitment, study metrics monitoring, and documentation activities.
  • Ensure sites and CRAs comply with study protocols, GCP, and applicable regulatory requirements.
  • Develop and manage clinical operations timelines, metrics, resourcing, budget, and related project activities.
  • Identify risks, escalate issues, and help implement corrective actions and mitigation strategies.
  • Track and reconcile clinical budgets related to monitoring visits and CRA allocation.
  • Serve as the clinical liaison among clients, site staff, CRAs, and internal teams.
  • Lead internal and external meetings and manage routine client communications and expectations.
  • Lead CRA and IHCRA onboarding, project training, and training sessions such as investigator meetings and conferences.
  • Review and support protocol deviation planning, reconciliation, and study documents such as monitoring plans, deviation plans, and case report forms.

Requirements

  • Bachelor's degree, preferably in a life science, nursing, pharmacy, or related field.
  • 5 years of clinical research experience within a CRO, pharmaceutical, or biotechnology company.
  • At least 2 years of experience as a clinical team lead preferred.
  • At least 2 years of on-site monitoring experience.
  • Proven leadership experience leading teams within a CRO or pharmaceutical setting.
  • Strong knowledge of GCP, regulatory requirements, clinical trial processes, and documentation.
  • Excellent interpersonal and communication skills with the ability to build relationships with clients and teams.
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Proactive, solutions-oriented mindset with the ability to drive decisions and lead initiatives.
  • Experience using clinical trial management software and EDC systems.
  • Must submit CV in English.

Benefits

  • Remote permanent role with occasional travel for site visits and client meetings.
  • Work-life balance flexibility.
  • Opportunity to work in a stable company environment with financial, workforce, and corporate stability.

Interested in this position?

Apply directly on the company website

Apply Now

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