1,000+ matching jobs for “Design Project Manager”

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Thermo Fisher Scientific

Senior Clinical Team Manager

Seoul, Seoul, South Korea

Join Us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of Innovation Job Summary APAC Senior Clinical Team Manager supporting …

Added Oct 16, 2026

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Campbell's

Associate Manager, Training

Lakeland, Florida, United States

Full time
Regular

Pay posted by employer$89,800–$123,500

How you will make history here... The Associate Manager, Training is responsible for leading, developing, and executing comprehensive training and development …

Added Oct 27, 2026

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PulteGroup

Area Construction Manager

Dublin, Ohio, United States

Full time
Regular

… onsite attendance for meetings held at our Division Office located in Dublin, Ohio . The Area Construction Manager is responsible for supervising Assistant Construction Managers, Construction Managers and/or Senior …

Added Nov 3, 2026

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Lowe's

Manager Recruitment Marketing

Mooresville, NC (SSC) 1999

… of coffee), work out or get a check-up – we invest in you so you can find your inspiration. Your Impact The Manager of Recruitment Marketing will be responsible for designing the recruitment marketing and media strategies …

Added Oct 27, 2026

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Lennar

Division Environmental Manager

Ocala, Florida, United States

… timely OSHA recordkeeping and reporting, and track closure of findings through to verified completion. Design and deliver targeted environmental and safety training programs for field Associates, trade partners, and …

Added Nov 7, 2026

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Nvidia

Manager, Software Architecture

Santa Clara, California, United States

… join the team and see how you can make a lasting impact on the world. We are Seeking a Software Engineering Manager for our applied research team within NVIDIA’s Networking Systems & Software Architecture group. This role …

Added Oct 31, 2026

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Abbott Laboratories

EMEA Content Manager

Maidenhead, England, United Kingdom

… they need to live their healthiest life. We are seeking an experienced and forward‑thinking EMEA Content Manager to build and scale the next generation of commercial capabilities across the region. About the Role Abbott …

Added Oct 23, 2026

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KeyCorp

Product Manager III

Buffalo, New York, United States

Full time

Pay posted by employer$96,000–$181,000 per year

The Product Manager III is responsible for the strategic planning, development and management of new and existing product …

Added Nov 3, 2026

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Thermo Fisher Scientific

인재풀 - Clinical Trial Manager

Remote, Korea, Republic of

… status updates (including rejection notifications) may not be provided. Join Us as a Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the …

Added Oct 16, 2026

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Thermo Fisher Scientific

Clinical Trial Manager - FSP

Mumbai, Maharashtra, India

Join oin Us as a Clinical Trial Manager, managing studies locally in INdia for one of our clients. Make an Impact at the Forefront of Innovation …

Added Oct 16, 2026

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Nvidia

Product Program Manager

Santa Clara, California, United States

of Product Program Manager. Our team takes pride in building a wide range of products — Data center related products, Jetson devices, …

Added Oct 27, 2026

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GE Vernova

Power Systems Tender Manager

Stafford, England, United Kingdom +1 location

Summary Job Description Power Systems Tender Manager GE Vernova is looking for an exceptional Power Systems Tender Manager to join our Tendering team for Grid …

Added Oct 27, 2026

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Amgen

Manager Information Systems

India - Hyderabad

Full time
Regular

As a Manager of Information Systems at Amgen, you will provide leadership and oversight to the organization's …

Added Oct 15, 2026

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Abbott Laboratories

Manager Data Science

Mumbai, Maharashtra, India

… and manage analysis and modelling as well as communicate results to the senior stakeholders. • Lead the design and development of advanced analytical and AI/ML solutions, transforming large data into meaningful …

Added Oct 15, 2026

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Raymond James Financial

Manager, ServiceNow Solutions

St. Petersburg, Florida, United States +2 locations

Permanent

Summary The Manager, ServiceNow Solutions is responsible for leading a team of ServiceNow Business Analysts and Developers that …

Added Nov 3, 2026

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Verizon

Software Development - Senior Manager

New York City, New York, United States

Remote
Senior

Pay posted by employer$200,014–$238,000 per year

… trust in how we show up, everywhere & always. Want in? Join the #VTeamLife. What you'll be doing… Lead the design, development and architecture of IT systems and end to end solutions; analyze business needs, re-design …

Added Oct 29, 2026

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Procter & Gamble

CF HSE Manager

HYDERABAD OFFICE APAC PSC GDOP

… you will collaborate with peers and receive both formal training as well as day-to-day mentoring from your manager dynamic and encouraging work environment– employees are at the centre, we value every individual and …

Added Oct 27, 2026

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Mastercard

Manager, Software Engineering

O'Fallon, Missouri, United States

Pay posted by employer$140,000–$231,000 USD

… services that help people, businesses and governments realize their greatest potential. Title and Summary Manager, Software Engineering Job Overview Lead a team of software engineering professionals responsible for …

Added Oct 28, 2026

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Palo Alto Networks

Events Experience Manager

Office - USA - CA - Headquarters

We're looking for an Event Experience Manager to join our growing Global Events organization. This is an exciting opportunity for an experienced event …

Added Oct 27, 2026

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Marsh & McLennan

Manager, Rewards Advisory

Kuala Lumpur - Corporate

… arrangement. Join the Rewards team to manage local and regional benefits, assist with flexible benefit design, and collaborate with our global counterparts. You will gain global career exposure, learn from top …

Added Oct 27, 2026

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Thermo Fisher Scientific

Senior Clinical Team Manager

Seoul, Seoul, South Korea

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of Innovation

Job Summary

APAC Senior Clinical Team Manager supporting the current Revolution Medicines portfolio and potentially other clients in the future.
South Korea is the preferred hiring location.
Recent Hematology & Oncology (HemOnc) experience is a must.
Lead moderate-to-high complexity clinical studies independently, with potential Regional Lead CTM/CSM responsibilities.
Relevant experience in regional/global studies, Phase 1/3, dose escalation, cohort/basket studies, and master protocols preferred.
8+ years of relevant experience; strong English communication and leadership skills required.

The Senior Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. Interprets data on complex issues and makes good business decisions with support from line management. The role involves working to ensure that all clinical deliverables meet the customer's time/quality/cost expectations, and maintaining profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. Typically the Senior Clinical Trial Manager works independently on projects of moderate to high complexity, and may assume regional lead or Clinical Study Manager responsibilities.

What You'll Do:
• Manage all clinical operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Lead CTM responsibilities on regional level, Clinical Study Manager (CSM) responsibilities or take on additional responsibilities, e.g. process improvements, manage complex programs, have wider management or project coordination responsibilities.
• Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
• Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
• Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor clinical trials to assess performance and ensure contractual obligations are met. May routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
• Communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
• May coordinate all start-up activities, and ensure that essential document quality meets the expectation of Regulatory Compliance Review. Ensure timely regulatory submissions (if appropriate) are addressed. Reviews and follows up on all questions raised by ethics committees. Responsibility may vary based on project timelines.
• Provide input into preparation of forecast estimates for clinical activities.
• Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.
• In North America, where assigned to GPHS (Government & Public Health Studies) projects, may have limited line management responsibilities.

Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities:
• Strong leadership skills, effective at mentoring and training, and capable of motivating and integrating teams.
• Strong planning and organizational skills to enable effective prioritization of workload and workload of team members
• Strong interpersonal and problem solving skills to enable working in a multicultural matrix organization
• Solid understanding of change management principles
• Comprehensive understanding of the practices, processes, and requirements of clinical monitoring
• Strong judgment, decision making, escalation, and risk management skills
• Effective oral and written communication skills, including English language proficiency
• Capable of evaluating own and team members workload against project budget and adjust resources accordingly
• Strong financial acumen and knowledge of budgeting, forecasting and fiscal management
• Strong attention to detail
• In-depth understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
• Strong computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
• Capable of independently managing clinical only studies.

Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Frequently drives to site locations and frequently travels both domestic and international.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.

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