Sr. Clinical Project Manager - Epilepsy

Jobgether

Oregon

Hybrid

USD 130,000 - 170,000

Full time

7 days ago
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Benefits offered by this job

Remote US-based
More than 50% FTE
Autonomy and collaboration

Job summary

Jobgether is seeking a Sr. Clinical Project Manager - Epilepsy in the United States. The role leads complex CNS trials, including rare epilepsy indications, from start-up to close-out, ensuring quality and sponsor satisfaction.

You will collaborate with a neuroscience team and external stakeholders to drive timelines, budgets, and regulatory compliance. The ideal candidate has 7+ years in clinical trials, CRO experience, and strong English communication skills.

Qualifications

  • Academic degree, preferably in a biomedical or related scientific field.
  • Previous experience in a Contract Research Organization (CRO) is required.
  • Direct experience managing epilepsy clinical trials, ideally rare epilepsy indications, is essential.

Responsibilities

  • Lead the delivery of complex CNS trials with a focus on rare epilepsy studies, ensuring timelines and budgets.
  • Oversee studies from start-up through close-out.
  • Develop study-specific documentation with Compliance and study teams.

Skills

Clinical PM
Epilepsy trials
CRO experience
Stakeholder mgmt
English proficiency

Education

Biomedical degree

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Clinical Project Manager - Epilepsy based in the United States. This is an opportunity for an experienced clinical research professional to lead complex clinical trials focused on epilepsy, with particular emphasis on rare epilepsy indications. You will oversee studies from start-up through close-out, ensuring delivery against agreed scope, timelines, budgets, and quality standards. Working within a specialized neuroscience team, you will coordinate multidisciplinary experts and serve as a trusted day-to-day partner to sponsors. The role offers considerable autonomy, close collaboration with experienced clinical operations teams, and the opportunity to contribute to studies addressing significant unmet medical needs. Your expertise will help advance clinical development while maintaining the highest standards of regulatory compliance and operational excellence.

Accountabilities
  • Lead the delivery of complex clinical trials in CNS, with a strong focus on rare epilepsy studies, ensuring milestones and services meet sponsor expectations and agreed project scope, timelines, and budgets.
  • Oversee clinical projects throughout their full lifecycle, from study start-up to close-out.
  • Develop study-specific documentation in collaboration with Compliance and relevant study teams.
  • Monitor project progress against plans, key performance indicators, timelines, and budgets, implementing adjustments when necessary.
  • Identify, assess, and proactively mitigate project risks and operational challenges.
  • Provide clear and timely progress updates to sponsors, internal stakeholders, and steering committees.
  • Serve as the primary day-to-day contact for sponsors and project teams, building effective working relationships and maintaining alignment.
  • Manage project finances and contribute to proposals, budget development, and bid defense meetings.
  • Resolve complex project challenges through effective communication, collaboration, and stakeholder engagement.
  • Identify opportunities for process improvements and contribute to the continued development of the clinical project management function.
Requirements
  • Academic degree, preferably in a biomedical or related scientific field.
  • Previous experience working within a Contract Research Organization (CRO) is required.
  • Direct experience managing epilepsy clinical trials, ideally involving rare epilepsy indications, is essential.
  • At least 7 years of clinical trial experience within the pharmaceutical industry and/or CRO environment.
  • Minimum of 5 years of experience in clinical project management, including significant experience within a CRO.
  • Experience in additional neurological or neuroscience indications is highly desirable.
  • Extensive experience managing multinational clinical studies and coordinating international teams.
  • Strong knowledge of ICH-GCP guidelines and applicable clinical research regulations.
  • Excellent command of English, with strong written and verbal communication skills.
  • Proven ability to establish and maintain trusted relationships with sponsor stakeholders, including senior executives and CEOs.
  • Strong project leadership, organizational, financial management, and problem-solving capabilities.
  • Ability to work autonomously while collaborating effectively with multidisciplinary teams and external stakeholders.
Benefits
  • Remote consulting opportunity based in the United States.
  • Flexible engagement structure with a commitment of more than 50% FTE.
  • High level of autonomy in managing clinical projects.
  • Opportunity to work alongside experienced clinical operations professionals within a specialized neuroscience team.
  • Stable and collaborative working environment with low team turnover.
  • Opportunity to contribute to clinical research focused on rare epilepsy and other important therapeutic areas.
How Jobgether works

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

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