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

Role Description - 7+ years in Project Management (preferably in an outsourcing services or consultancy environment) - Proven technical background, being able to bridge the gap between non-technical stakeholders and engineering requirements - Skilled at orchestration of the project backlog to balance objectives with day-to-day delivery needs - Capable of overseeing timelines, budgets, and risks, while providing clear reporting (e.g., sprint burn-downs, progress updates) to stakeholders - Ability to analyze processes, identify bottlenecks, and propose data-driven improvements - Great written and verbal communication skills to convey product requirements to both technical and non-technical audiences - Experience working with remote / 3rd party team members in an Agile environment - Experience in running Scrum and Kanban is a must - Critical thinking skills to assess feature requests, prioritize effectively, and measure impacts - A creative, problem-solving attitude that seeks out new opportunities or improvements Company Description

Role Description Visionary Construction, Inc. is seeking an experienced Fractional Construction Project Manager to support active and incoming federal construction and facilities contracts on an as-needed, contract basis. This is not a staff role; it is a high-impact engagement for someone who knows how to step in, get oriented fast, and deliver. You will work alongside our internal operations team and directly support project execution across multiple agencies and geographies. This role will be 1099. - Oversee and manage multiple federal construction projects from notice to proceed through final acceptance, including punch-out and closeout documentation. - Coordinate with subcontractors, suppliers, and government representatives (COR/QAR) to ensure project milestones and deliverables are met on schedule. - Develop, maintain, and submit Quality Control Plans (QCPs) in accordance with contract requirements, including administration of the three phases of control: Preparatory, Initial, and Follow-Up. - Manage and maintain submittal registers, RFI logs, re-work/deficiency logs, and daily QC reports in formats acceptable to the Government. - Conduct site visits to monitor progress, verify compliance with approved submittals, and document field conditions. - Prepare and manage project budgets, track actual costs against contract values, and flag margin risk early. - Support preparation and review of AIA G702/G703 payment applications and coordinate subcontractor compliance documentation including WH-347 certified payroll under Davis-Bacon requirements. - Assist with WAWF invoice preparation and documentation support for government invoicing milestones. - Serve as a point of coordination between field supervisors, the internal operations team, and the contracting officer or designated representative. - Identify and document changes in scope, prepare or support requests for equitable adjustment (REAs) or contract modifications as needed. - Maintain project records in a format that supports audit readiness, including as-built drawings, O&M manuals, and warranty documentation at closeout. - Participate in weekly compliance meetings and provide written status updates to leadership. Qualifications - Minimum 7 years of construction project management experience, with significant federal contracting exposure (FAR/DFARS framework required, not preferred). - Demonstrated experience managing government construction contracts across agencies such as GSA, DoD, USACE, DoI, or DHS. - Working knowledge of Davis-Bacon Act compliance, certified payroll review, and subcontractor compliance monitoring. - Familiarity with WAWF or equivalent government invoicing platforms. - Experience developing or administering Quality Control Plans per USACE EM 385-1-1 or equivalent federal standards. - Proficiency in managing submittals, RFIs, and change order documentation on government projects. - Strong command of AIA payment application standards (G702/G703). - Ability to manage projects across multiple states and/or remote locations with limited in-person support structure. - Comfortable working within a small business environment where you will wear multiple hats and operate with a degree of autonomy. - Bachelor's degree in Construction Management, Civil Engineering, or a related field, or equivalent experience in lieu of degree. - Relevant certifications (PMP, LEED, CQM-C) are a strong plus. OSHA 30 required. - Proficiency in project management software; experience with Procore, Buildertrend, or equivalent is a plus. Benefits - Bonus based on performance - Flexible schedule - Opportunity for advancement Company Description Visionary Construction, Inc. d/b/a Visionary Services is a certified Woman-Owned Small Business (WOSB) and SBA 8(a) program participant with over a decade of performance on federal construction and facilities contracts. Our project portfolio spans GSA, USACE, DoD, DoI, DHS, and other federal agencies, ranging from HVAC and MEP replacements to large-scale renovations and site work across the continental U.S., Puerto Rico, and the U.S. Virgin Islands. We operate with a lean, capable team and expect the same from the partners we bring in. Flexible work from home options available.

Role Description Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Qualifications - Relevant experience in clinical research. - Strong communication and collaboration skills. - Ability to work in a fast-paced environment. - Passion for advancing medical research. Requirements - Experience with clinical trials and regulatory processes. - Proficiency in data analysis and interpretation. - Strong organizational skills and attention to detail. Benefits - Competitive salary and performance-based bonuses. - Comprehensive health benefits. - Flexible working hours and remote work options. - Opportunities for professional development and growth. Company Description Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in: - Cell and gene therapy - Vaccines and infectious diseases - Ophthalmology - Rare diseases - Neuroscience