EPM Scientific
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Clinical Trial Manager
role at
EPM Scientific This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$150,000.00/yr - $155,000.00/yr Compensation: $150,000-155,000 + 15% bonus + Lucrative Stock Options Package + 4 Weeks PTO and 2 company shutdowns per year (6 weeks total PTO) Company Summary: A cutting-edge biotech company that's revolutionizing drug discovery using Nobel Prize-winning science is currently building out its Clinical Operations team ahead to support its highly anticipated Phase 3 study. Their technology allows scientists to watch proteins move in real time inside living cells, offering a deeper understanding of disease and drug effects. With AI and automation, they analyze millions of cells daily, driving a robust pipeline that includes a lead candidate entering Phase 3 for an Oncology indication, along with programs in neurology and immunology. Backed by over $1.1 billion in funding and led by industry veterans behind some of the most impactful therapies in recent years, this is a unique chance to join a team poised to become a major force in pharma. Primary Responsibilities: Partner with Clinical Study Operations to provide strategic direction and hands-on oversight for the internal execution of global clinical research studies, ensuring timely, cost-effective delivery of high-quality data. Design and implement operational strategies to support the successful internal management of oncology-focused clinical trials. Work closely with cross-disciplinary teams-including data science, medical affairs, regulatory affairs, and clinical investigators-to drive operational excellence and accelerate the generation of reliable study outcomes. Oversee all trial initiation activities, coordinating with internal teams responsible for site engagement, monitoring, and vendor performance to streamline site selection, feasibility evaluations, and study documentation preparation. Collaborate with internal monitoring and site engagement teams to ensure efficient site activation, training, and oversight, maintaining compliance with study protocols, regulatory standards, and international clinical research guidelines. Foster strong working relationships with clinical sites, including investigators and site staff, to support patient enrollment and retention efforts. Track study milestones and performance metrics, proactively identifying risks or deviations and implementing corrective measures to preserve study integrity and timelines. Ensure adherence to global regulatory standards, including ICH-GCP and applicable health authority requirements, throughout the study lifecycle. When needed, coordinate with third-party service providers such as CROs, labs, and imaging vendors to ensure timely and quality deliverables. Contribute to the drafting and review of essential study materials, including protocols, informed consent documents, case report forms, and internal procedural documents. Prepare operational tools and workflows to ensure consistent adherence to study plans and administrative processes. Lead the organization and maintenance of essential study documentation, including oversight of the central trial file and site-level records. Conduct regular audits and reviews of the sponsor's trial documentation to ensure completeness, accuracy, and regulatory compliance. Ideal Qualifications: Experience working on Oncology Trials Experience working in an
FSP
model Experience working on trials in an insourced model where you were responsible for interacting directly with clinical trial sites. Experience being a CTM for at least 5 years Sr. Manager level, Full-time, Research position.
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Clinical Trial Manager
role at
EPM Scientific This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$150,000.00/yr - $155,000.00/yr Compensation: $150,000-155,000 + 15% bonus + Lucrative Stock Options Package + 4 Weeks PTO and 2 company shutdowns per year (6 weeks total PTO) Company Summary: A cutting-edge biotech company that's revolutionizing drug discovery using Nobel Prize-winning science is currently building out its Clinical Operations team ahead to support its highly anticipated Phase 3 study. Their technology allows scientists to watch proteins move in real time inside living cells, offering a deeper understanding of disease and drug effects. With AI and automation, they analyze millions of cells daily, driving a robust pipeline that includes a lead candidate entering Phase 3 for an Oncology indication, along with programs in neurology and immunology. Backed by over $1.1 billion in funding and led by industry veterans behind some of the most impactful therapies in recent years, this is a unique chance to join a team poised to become a major force in pharma. Primary Responsibilities: Partner with Clinical Study Operations to provide strategic direction and hands-on oversight for the internal execution of global clinical research studies, ensuring timely, cost-effective delivery of high-quality data. Design and implement operational strategies to support the successful internal management of oncology-focused clinical trials. Work closely with cross-disciplinary teams-including data science, medical affairs, regulatory affairs, and clinical investigators-to drive operational excellence and accelerate the generation of reliable study outcomes. Oversee all trial initiation activities, coordinating with internal teams responsible for site engagement, monitoring, and vendor performance to streamline site selection, feasibility evaluations, and study documentation preparation. Collaborate with internal monitoring and site engagement teams to ensure efficient site activation, training, and oversight, maintaining compliance with study protocols, regulatory standards, and international clinical research guidelines. Foster strong working relationships with clinical sites, including investigators and site staff, to support patient enrollment and retention efforts. Track study milestones and performance metrics, proactively identifying risks or deviations and implementing corrective measures to preserve study integrity and timelines. Ensure adherence to global regulatory standards, including ICH-GCP and applicable health authority requirements, throughout the study lifecycle. When needed, coordinate with third-party service providers such as CROs, labs, and imaging vendors to ensure timely and quality deliverables. Contribute to the drafting and review of essential study materials, including protocols, informed consent documents, case report forms, and internal procedural documents. Prepare operational tools and workflows to ensure consistent adherence to study plans and administrative processes. Lead the organization and maintenance of essential study documentation, including oversight of the central trial file and site-level records. Conduct regular audits and reviews of the sponsor's trial documentation to ensure completeness, accuracy, and regulatory compliance. Ideal Qualifications: Experience working on Oncology Trials Experience working in an
FSP
model Experience working on trials in an insourced model where you were responsible for interacting directly with clinical trial sites. Experience being a CTM for at least 5 years Sr. Manager level, Full-time, Research position.
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