Sr. Clinical Project Manager - Epilepsy

P95•,

6d•Remote

About The Position

P95 Julius Clinical is a global, full-service Clinical Research Organization (CRO) formed through the merger of P95 and Julius Clinical. The company delivers integrated clinical development and real-world evidence solutions across five continents, with regional hubs in Africa, Latin America, North America, Southeast Asia, and Europe. Its team of 500 professionals has conducted more than 1,000 clinical trials in over 50 countries, supporting pharmaceutical, biotech, and public health partners through full-service and modular CRO capabilities across the development lifecycle and post-marketing phases. The Senior Clinical Project Manager will work remotely in the U.S. within the neuroscience business unit, leading complex clinical trials from start-up through close-out. The role is focused on CNS, particularly rare epilepsy studies, and is expected to ensure delivery within project scope, budget, and timelines while meeting client expectations. The position manages multidisciplinary teams, serves as the primary day-to-day contact for sponsors, and promotes compliance with ICH-GCP, protocols, SOPs, and relevant regulations. P95 Julius Clinical seeks someone with a strong background in rare epilepsy studies to strengthen its existing expertise. The company describes its operations teams as highly experienced, with low turnover, and its CPMs as having substantial autonomy.

Requirements

Academic degree, preferably in a biomedical field.
CRO experience.
Epilepsy trial experience, with a strong rare epilepsy study background sought.
At least 7 years of experience in clinical trials in pharma and/or CRO settings.
At least 5 years of experience as a Project Manager, including significant CRO experience.
Extensive multinational study experience.
Excellent command of English.
Strong knowledge of ICH-GCP and relevant regulations.
Proven ability to build strong relationships with small sponsor stakeholders, including CEOs.

Nice To Haves

Experience with other neuroscience indications.

Responsibilities

Lead complex clinical trials from start-up to close-out, delivering services and milestones in line with client expectations, project scope, schedules, and budget.
Manage multidisciplinary project teams.
Develop study-specific documentation in collaboration with Compliance and study teams.
Monitor progress against plans, KPIs, and budgets, and adjust as needed.
Identify and mitigate risks proactively.
Report progress to sponsors, internal stakeholders, and steering committees.
Act as the day-to-day contact for sponsors and project teams.
Drive process improvements and contribute to departmental growth.
Manage project finances and support proposals and bid defense meetings.
Resolve complex challenges through effective stakeholder engagement.
Ensure compliance with ICH-GCP, protocols, SOPs, and relevant regulations.