Veridix AI is the technology, data, and AI arm of the Emmes Group, a leading full-service contract research organization (CRO) with over 47 years of experience in supporting clinical research across more than 70 countries. With industry-leading capabilities in cell and gene therapy, vaccines, infectious diseases, and ophthalmology, Emmes is one of the top clinical service providers to the U.S. government and is rapidly expanding its presence in biopharma. Veridix AI develops advanced eClinical solutions, powering clinical trials through patient data collection, randomization, biospecimen tracking, and data quality monitoring. Our cutting-edge AI innovations, including Generative AI (GenAI) capabilities, are transforming clinical trial timelines by streamlining processes from document authoring to automating study builds. Our “Character Achieves Results” culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships, and Intellectual Curiosity. If you share our motivations and passion in research, come join us!
Clinical Project Manager II
Location
South Carolina
Posted
7 days ago
Salary
$14 - $16 / hour
Seniority
Lead
No structured requirement data.
Job Description
Clinical Project Manager II
Emmes Group
Role Description The Clinical Project Manager (CPM) II is responsible for delivering clinical and research initiatives that support complex IT and life sciences programs. This role leads cross-functional project teams across technology implementations, clinical study operations, data integrations, and regulatory-compliant systems. The CPM II brings hands-on study management experience spanning participant enrollment, informed consent, data collection, and research participant engagement — ensuring that operational execution aligns with both scientific objectives and compliance requirements. The CPM II cultivates collaborative relationships with project and client stakeholders, coordinating across teams to ensure study goals are achieved and deliverable timelines are met. This role drives implementation strategy, maintains operational plans and documentation, and continuously optimizes study processes to support high-quality clinical research delivery. The CPM II is expected to maintain current awareness of industry best practices and emerging trends in study management, actively contributing that knowledge to strengthen Essex's methodologies and commitment to continuous improvement. Qualifications - Bachelor's degree in public health, life sciences, clinical research, or a related field (Master's preferred); or a commensurate combination of education and experience - 3–5+ years of experience in clinical research operations, study implementation, clinical data management, or a related discipline - Familiarity with IRB processes, regulatory requirements, and clinical research compliance standards - Experience with oncology and/or rare disease studies is desirable Requirements - Lead the end-to-end execution of clinical trials and observational studies, from protocol design through final clinical study report, applying best practices across all project phases — initiation, planning, execution, monitoring, and close-out - Develop and maintain integrated, cross-functional project plans to support study tracking, milestone management, and oversight across all workstreams - Anticipate potential barriers, identify project risks, and propose mitigation strategies; adhere to established governance structures and processes for assigned projects - Lead and coordinate cross-functional study team activities, including patient engagement, clinical monitoring, data management, biostatistics, and safety, to ensure proper conduct and timely study completion - Collaborate with internal teams, contractors, and vendors — including functions such as finance, R&D, regulatory, and marketing — to align efforts and achieve study goals and objectives - Ensure communication plans are in place and maintained to support effective information flow among all study and project stakeholders - Contribute to database design and development with a focus on data abstraction, report generation, and quality assurance to support effective data monitoring - Maintain compliance with Good Clinical Practice (GCP), regulatory requirements, and applicable Essex and client policies and procedures - Participate in quality assurance activities to ensure deliverables meet contractual requirements and key performance indicators are monitored and achieved - Track and manage adherence to budget, scope, and schedule requirements throughout the project lifecycle - Organize and facilitate project meetings, including scheduling, preparation of materials, meeting minutes, and follow-up on action items - Prepare monthly status reports and project-specific documentation in accordance with reporting requirements - Complete required Essex and client training and maintain ongoing awareness of relevant policies to ensure continuous compliance Benefits - Flexible Approved Time Off - Tuition Reimbursement - 401k Retirement Plan - Work From Home Anywhere in the US - Maternal/Paternal Leave - Casual Dress Code & Work Environment
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