Jobs in the United States

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VL
Scientist - Process Research & Development
Veranova L P
Devens, MA
- $100,000 to $110,000 USD / year
…to large-scale chemical reactions and generates high-quality data that supports project decision-making and innovation. Working under the guidance of technical leads, the role contributes…
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Software Development Engineer, Global Tax Services - Data
Amazon.com Services LLC
Seattle, WA
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Software Dev Engineer-III, Route 53 Resolver
Amazon Development Center U.S., Inc.
Seattle, WA · Herndon, VA
…we’re the people who keep the cloud running. We support all AWS data centers and all of the servers, storage, networking, power, and cooling equipment that ensure our customers have…
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Sr. Mechanical Design Engineer, Data Center Design Engineering
Amazon Data Services, Inc.
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Mechanical Design Engineer, Data Center Design Engineering
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Austin, TX · Seattle, WA · Herndon, VA
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Data Center Technician
Amazon Data Services, Inc.
Berwick, PA
Work shifts longer than 8 hours to support 24/7 operations (covering both night and day shifts)
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Data Center Technician
Amazon Data Services, Inc.
Berwick, PA
Work shifts longer than 8 hours to support 24/7 operations (covering both night and day shifts)
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Data Center Technician
Amazon Data Services, Inc.
Berwick, PA
Work shifts longer than 8 hours to support 24/7 operations (covering both night and day shifts)
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Account Manager, ENT - Chicago
INTEGRA LIFESCIENCES SALES LLC
United States
Proctor Acclarent-trained physicians during their initial procedures to provide guidance, gather procedure data, and recommend training certification when ready, and provide customer…
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BM
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Stamford, CT
- $80,000 to $100,000 USD / year
Maintain and update the database of market and property data.
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Dallas, TX
…compliance, preliminary scoping, preliminary engineering, mapping and data analysis, benefit-cost analysis, narrative development, state and federal agency engagement, desktop environmental…
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…Supply Support, Maintenance Planning and Management, Technical Data, Support Equipment, Sustaining Engineering, or Design for…
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The Options Clearing Corporation
United States
A hybrid work environment, up to 2 days per week of remote work
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- $55,000 to $65,000 USD / year
…matters. From emails and text messages to hard-copy documents and data stored in the cloud, we help clients organize, review, and produce digital evidence accurately, securely, and…
Added 1 min ago
Associate Director, Integrated Business Planning - Network Planning - (Food/ Burt's)
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Alpharetta, GA · Durham, NC
Synthesizes complex demand, supply, and financial data into clear insights, risks, tradeoffs, and recommendations.
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Senior Buyer (Procurement)
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Senior Treasury Analyst, Capital Markets & Risk
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Hybrid - 3 days per week in office, 2 days remote
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Account Executive - Phoenix, East Valley
US Foods, Inc.
Regional Phoenix, AZ
Travel required; anticipated field time at least four days per week
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Staff Auditor (Hybrid: Onsite and Remote Work)
US Foods, Inc.
Rosemont, IL
2 years of related work experience required (in role or similar role)
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Lead, Career Center - Dallas
Equus
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Observes, receives and obtains relevant customer information for data entry and prepares customer files.
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Workforce Media Specialist - Dallas
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Strong analytical skills and ability to interpret data and information; must be organized and detailed in the collection, review and analysis of data and information.

Cytrellis Biosystems

Clinical Project Manager

Remote, United States

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Job details

Posting language: English
Posted: Nov 10, 2026

Original job description

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Description

The Clinical Project Manager will lead the planning, execution, and oversight of clinical studies supporting an aesthetic medical device portfolio. This individual will manage study operations from start-up through closeout, ensuring studies meet established timelines, budgets, quality standards, and applicable regulatory requirements. The ideal candidate combines hands-on clinical operations experience with strong project management skills and the ability to build effective relationships with investigators, study sites, vendors, and cross-functional colleagues. This role requires a proactive, detail-oriented professional who can translate clinical objectives into practical execution plans while prioritizing participant safety and data integrity.

Key Responsibilities

Clinical Study Planning and Execution

Manage assigned clinical studies throughout the study lifecycle, including feasibility, site selection, start-up, enrollment, follow-up, and closeout.
Develop and maintain study plans, timelines, budgets, resource forecasts, and risk mitigation strategies.
Coordinate the development and review of protocols, informed consent forms, case report forms, study manuals, and other essential study documents.
Track study progress, identify operational barriers, and implement corrective actions to keep projects on schedule.
Provide clear updates to leadership on milestones, enrollment, spending, risks, and decisions requiring escalation.

Site and Investigator Management

Serve as a primary operational contact for investigators, research coordinators, and clinical study sites.
Coordinate site qualification, initiation, monitoring, and closeout activities.
Ensure site personnel receive appropriate training on protocols, study procedures, documentation, and device handling.

Quality, Compliance, and Participant Safety

Oversee study execution in accordance with approved protocols, company procedures, and applicable clinical research requirements.
Partner with Medical, Regulatory Affairs, and Quality Assurance on adverse event documentation, safety escalation, and applicable reporting activities.
Support audits and inspections and drive timely resolution of findings.

Vendor, Budget, and Cross-Functional Management

Manage external service providers as needed.
Coordinate scopes of work, deliverables, vendor performance, purchase orders, and invoice review.
Contribute to clinical study reports, abstracts, presentations, and publications in collaboration with relevant subject matter experts.

Operational Improvement

Develop and improve clinical operations templates, tools, workflows, and standard operating procedures.
Support a culture of collaboration, scientific rigor, continuous improvement, and patient-centered research.

Requirements

Bachelor’s degree in a scientific, healthcare, life sciences, or related discipline, or an equivalent combination of education and relevant experience.
Five or more years of medical device clinical research experience, including at least two years managing clinical studies or substantial clinical study workstreams.
Working knowledge of Good Clinical Practice and applicable FDA requirements for medical device investigations, informed consent, and institutional review board oversight.
Demonstrated ability to manage study timelines, budgets, risks, and competing priorities.
Experience with clinical documentation, monitoring activities, data review, and audit readiness.
Strong written and verbal communication, organizational, problem-solving, and relationship-management skills.
Ability to work independently while collaborating effectively across functions.
Willingness to travel to study sites and company meetings as required.

Preferred Qualifications

Experience in medical aesthetics, dermatology, plastic surgery, or related procedural specialties.
Familiarity with standardized clinical photography, blinded assessments, patient-reported outcomes, and aesthetic outcome measures.

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Jobs in the United States