Clinical Project Manager
TLDR
Own end-to-end planning and delivery of neuromonitoring clinical studies across sites, ensuring on-time, within-budget execution under global regulatory standards.
- Lead end-to-end management of clinical studies, including planning, execution, timelines, budgets, and risk mitigation while ensuring alignment with study objectives and regulatory requirements.
- Oversee site selection, feasibility assessments, contract negotiations, initiation, monitoring, and close-out activities across clinical trial sites.
- Ensure compliance with FDA regulations (21 CFR Parts 50/56/812), ISO 14155, GCP, and internal SOPs throughout all study phases.
- Manage study documentation including protocols, CRFs, ICFs, monitoring reports, study manuals, and clinical evaluation materials.
- Track enrollment, study KPIs, and site performance, proactively identifying and resolving operational or data-related issues.
- Coordinate clinical data activities such as query resolution, CRF completion, and data cleaning in collaboration with data management teams.
- Support audits and inspections while maintaining inspection-ready documentation and ensuring quality system adherence.
- Provide regular updates and reports to senior stakeholders, ensuring transparency on study progress and outcomes.
- Equity participation in the company
- Unlimited paid time off
- Health insurance with 50% employer contribution to premiums
- Dental insurance with 50% employer contribution
- Vision insurance with 50% employer contribution
- 401(k) retirement plan with up to 3% employer match
- Access to mental health and wellbeing resources
- Opportunity to contribute to breakthrough medical technology in neuromonitoring
- Collaborative, mission-driven environment focused on clinical innovation
Requirements
Candidates should have 3–6 years of clinical research experience, including at least 2 years in medical device clinical trials, with a strong understanding of regulatory frameworks and clinical operations workflows. You bring hands-on experience managing clinical sites or CRO partners and are confident working across multiple studies in parallel. You are familiar with FDA regulations, ISO 14155, and Good Clinical Practice (GCP) guidelines, and have used clinical systems such as EDC, eTMF, and CTMS. Strong organizational and communication skills are essential, along with the ability to interpret protocols, manage documentation, and coordinate cross-functional stakeholders effectively. Experience in neurology, neurocritical care, or ICU-based environments is a plus, as is exposure to clinical study reporting or regulatory documentation authoring. You combine operational discipline with adaptability in fast-moving clinical environments.
Benefits
Benefits
Equity Compensation
Equity participation in the company
Health Insurance
Vision insurance with 50% employer contribution
mission-driven environment
Collaborative, mission-driven environment focused on clinical innovation
Paid Time Off
401(k) retirement plan with up to 3% employer match
Wellness Stipend
Access to mental health and wellbeing resources
Jobgether runs the largest remote job platform, effectively linking job seekers with over 200,000 flexible and remote opportunities that match their unique skills and preferences. Our focus is on enhancing the hiring process, ensuring efficiency while prioritizing the candidate experience, particularly in the growing health and wellness sector.
- Founded
- Founded 2020
- Employees
- 11-50 employees
- Industry
- Professional Services