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A life sciences recruiting firm is looking for an experienced Clinical Project Manager to manage clinical projects in compliance with regulatory standards. The ideal candidate has over 3 years of experience and is responsible for leading cross-functional teams, budget forecasting, and ensuring project delivery on time. This role is remote and requires adaptability to regulatory changes while communicating effectively with stakeholders.
Ensure regulatory and GxP / GEP compliance; strong understanding of RA / MOH requirements and protocol implementation across regions. Plan, execute, and close clinical projects within scope, time, and budget; build timelines and manage risks, resources, and milestones. Oversee budget forecasting, burn rate monitoring, and scope change control. Lead cross‑functional teams (Clinical, Epi, DM, Stats, Reg, PVG) and foster collaboration and accountability. Communicate clearly with sponsors, vendors, and stakeholders; translate complex requirements into actionable steps. Anticipate issues, develop mitigation strategies, and adapt to regulatory or operational changes.
3+ years cross‑functional clinical PM experience. Strong regulatory / GEP and RA / MOH knowledge. Protocol interpretation across regions. End‑to‑end project delivery; risk, resource & milestone management. Study plan development; proficient with PM tools. Budget forecasting, burn‑rate & scope control. Clear stakeholder communication & actionable guidance. Risk anticipation, adaptability & solution‑oriented approach.
Start : asap Duration : 12 months Capacity : 2-3 days per week Location : remote