Clinical Trial Lead

Apply now Apply before: May 3, 2026

Are you passionate about Clinical Trials and energized by the end-to-end operational delivery of clinical trials in a small but fast growing biotech?

Alveus Therapeutics is seeking a Clinical Trial Lead (CTL) to join our global R&D organization.

The CTL will be responsible for the end-to-end operational delivery of one or more clinical trials, from study start-up through database lock and Clinical Study Report (CSR) completion. The CTL leads cross-functional trial teams and serves as the primary operational counterpart to the selected CRO, ensuring execution excellence in a lean, fast-moving biotech environment.

This role requires strong matrix leadership, hands-on operational expertise, and the ability to drive clarity, momentum, and accountability across internal and external stakeholders. The CTL thrives in ambiguity, brings a pragmatic and solutions-oriented mindset, and consistently delivers high-quality trials on time and within budget. You will report into our Head of Clinical Operations.

The salary range for this position is $160,000 – $ 210,000 per year + benefits.
Actual compensation will be determined based on experience, skills, internal equity, and location.

Required Qualifications

  • Bachelor’s degree in life sciences or related field required; advanced degree (MS, PharmD, PhD, MD or equivalent) preferred.
  • 10+ years of clinical operations experience within biotech or CRO environments.
  • Extensive hands-on experience leading Phase 1 and early Phase 2 trials.
  • Proven track record of independently delivering clinical trials from start-up to CSR.
  • Strong experience in CRO oversight and vendor management within outsourced models.
  • Experience in small or emerging biotech companies strongly preferred

Key Competencies

  • Deep knowledge of clinical trial execution and global regulatory requirements (ICH-GCP, FDA).
  • Strong matrix leadership skills with the ability to influence without formal authority.
  • Highly organized with exceptional project management capabilities.
  • Agile, proactive, and solutions-oriented with a strong sense of ownership.
  • Excellent communication and stakeholder management skills.
  • Ability to operate effectively in a lean, fast-paced, and evolving environment.

Key Responsibilities

  • Provide end-to-end operational leadership for assigned clinical trials, ensuring alignment with overall development strategy and company objectives.
  • Lead the cross-functional Clinical Trial Team (CTT), including representatives from Medical, Regulatory, Biometrics and CMC
  • Develop and maintain integrated trial timelines from start-up and protocol finalization through CSR, proactively managing critical path activities.
  • Serve as the primary operational interface with the CRO Project Lead, ensuring clear oversight of the trial, performance metrics, and escalation pathways.
  • Actively participate in appropriate CRO vendor selection, contracting, and performance management to ensure high-quality and cost-effective execution.
  • Drive study start-up activities including country and site selection, feasibility, regulatory submissions, and first-patient-in readiness.
  • Write the protocol, coordinating SME input and drive the review and finalization process
  • Ensure compliance with ICH-GCP, FDA and other applicable regulatory requirements, and internal SOPs.
  • Identify, assess, and mitigate trial risks; maintain issue, action, and decision logs and escalate appropriately.
  • Collaborate with the Clinical Program Lead and Head of Clinical Operations to manage study budgets in partnership with Finance, ensuring financial discipline without compromising quality.
  • Ensure and support inspection and audit readiness; oversee implementation of corrective and preventive actions (CAPAs) when required.
  • Contribute to continuous improvement of clinical operations processes, systems, and digital solutions to enhance efficiency and scalability.

Key Characteristics

  • Extremely pro-active and solutions‑oriented
  • Calm, resilient, and effective under pressure
  • Naturally takes ownership and follows through
  • Enjoys building structure in fast‑moving, evolving environments
  • Thrives in a small, entrepreneurial team setting

Place of Work

Alveus is a global organization with R&D teams in both the United States and Denmark. To support effective collaboration across time zones and ensure alignment with our core development hubs, this remote full-time role is based on the U.S. East Coast. Once the new Alveus office is established, occasional in‑person attendance may be required, typically a few days per month.