Jobs in the United States

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Added 1 min ago
KS
Sr. Manager, Technology Transfer & Site Eng
Kelly Services
Orangeburg, NY
- $170,000 USD / year
…expansion that will establish new manufacturing capabilities. The program includes storage, blending, automated high-speed packaging operations, and drug-product processing in Class 7 and…
Added 1 min ago
KS
Sr. Manager, Technology Transfer & Site Eng
Kelly Services
Orangeburg, NY
- $170,000 USD / year
…expansion that will establish new manufacturing capabilities. The program includes storage, blending, automated high-speed packaging operations, and drug-product processing in Class 7 and…
Added 1 min ago
DDP [CVD] Technical Support Engineer - (E3)
Applied Materials, Inc
United States
…of our employees. We’re committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more…
Added 8 mins ago
AC
Ping SSO Engineer w. AI
AMERICAN CYBERSYSTEM
Denver, CO
- $65 to $70 USD / hour
We are seeking a skilled and experienced Identity and Access Management (IAM) professional to fill the role of IAM (SSO) Engineer. As an IAM Engineer, you will play a critical role in…
Added 13 mins ago
Technical Program Manager II, Integrated Infrastructure Planning, Google Cloud
Google
Sunnyvale, CA
…whether down the street or across the globe. As a Technical Program Manager at Google, you’ll use your technical expertise to lead complex, multi-disciplinary projects from start to finish.…
Added 20 mins ago
AS
Lead Commercialization
AT&T Services, Inc.
Remote, United States
- $143,800 to $215,800 USD / year
Program and Project Management: Coordinate teams and external partners to ensure timely, on-budget launches of commercialization initiatives and strategic programs.
Added 24 mins ago
Project Manager, Economic Development Southern Region
State of Indiana
North Vernon, IN
The Project Manager serves as the key Indiana Economic Development Corporation (IEDC) representative for select counties of the Southern Indiana Region. Responsible for management of IEDC…
Added 24 mins ago
Assembly Technician - 2nd or 3rd Shift
Precinmac
Indianapolis, IN
Major Tool & Machine (MTM) was founded in 1946, starting with only four employees to support the commercialization of the jet engine following World War II. Today, MTM is a contract…
Added 36 mins ago
J
QA Engineer/Developer
Jobgether
Remote, United States
- $80,000 to $98,000 USD / year
…performance of software solutions supporting a federal healthcare program. You will lead both manual and automated testing activities, helping deliver dependable applications that meet…
Added 39 mins ago
DIVISONAL ENGINEERING PROJECT MANAGER
Kingspan Insulated Panels - Open
Deland, FL · Columbus, OH
Summary: The Divisional Project Engineering Manager leads engineering projects with a focus on enhancing efficiency, ensuring compliance, and implementing robust process improvements to…
Added 43 mins ago
Senior Solution Architect
Children's Hospital
United States
…Cloud Services, Software Development, Enterprise Architecture, Project and Program Management, IT Operations, and Information Security. Teams collaborate on high-impact initiatives such as…
Added 47 mins ago
DIVISONAL ENGINEERING PROJECT MANAGER
All Kingspan and Affiliate Companies
Deland, FL · Columbus, OH
Summary: The Divisional Project Engineering Manager leads engineering projects with a focus on enhancing efficiency, ensuring compliance, and implementing robust process improvements to…
Added 49 mins ago
Assistant Manager, Creative Operations - North America
Estée Lauder Companies
NY · New York
· 3+ years of experience in creative operations or creative project management either from within an agency or brand environment.
Added 58 mins ago
Mechanical Design Engineer Stf - E4
Lockheed Martin
Littleton, CO · Littleton
…will work with other IPT Lead and functional integrators to support program execution and deliveries within cost and schedule…
Added 58 mins ago
Project Management & Planning Operations Rep Stf - E4
Lockheed Martin
Marietta, GA · Marietta
Project Management experience and skills developing and managing a resource loaded schedule.
Added 58 mins ago
Project Engineer Sr Stf - E5
Lockheed Martin
Cape Canaveral, FL · Cape Canaveral
At Lockheed Martin, we know mission success starts with taking care of our people. Our Total Rewards program is designed to attract top talent, support your well-being, and help you grow -…
Added 58 mins ago
Project Specialist Stf - E4
Lockheed Martin
Moorestown, NJ · Moorestown
This position is in support of SPY-1 Sustainment efforts across the US Multi Domain Combat Systems (MDCS) market segment as the SPY-1 Sustainment Lead. The SPY-1 Sustainment Lead, will be…
Added 58 mins ago
Application Management Intern
Rockland Trust
Rockland, MA
…for customers and colleagues. As part of the Application Risk Management program, you'll gain valuable exposure to how organizations identify risks, evaluate controls, and make informed…
Added 58 mins ago
Legal Intern
Rockland Trust
Rockland, MA
…attorneys, collaborate with fellow interns on a summer-long project, and see firsthand how legal advice supports business growth, innovation, and risk…
Added 58 mins ago
Commercial Credit Admin Intern
Rockland Trust
Rockland, MA
Project management and organizational effectiveness.
Added 58 mins ago
Business Intelligence Analyst
Rockland Trust
Rockland, MA
Project management and stakeholder communication.
Added 58 mins ago
B2B Marketing Intern
Rockland Trust
Rockland, MA
Support project management efforts to ensure deadlines and deliverables are met.
Added 1 hour ago
GI
Operations Supervisor
GFL Industries
Northville, MI
- $71,000 to $89,000 USD / year
Added 1 hour ago
Forestry Supv - Timebound
Consumers Energy
SAGINAW, MI
…position is not eligible for participation in the H-1B lottery program and is not eligible for current or future immigration sponsorship for a work…
Added 1 hour ago
Safety Performance Integration Engineer - Structure Performance (GPSSC)
General Motors
Warren, MI
Support engineering projects by demonstrating initiative, creativity, independent judgment, and project management throughout the vehicle development process.

Actalent

Clinical Project Leader III (Homebased)

Durham, NC, United States

$80 to $90 USD / hour

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Job details

Pay: $80 to $90 USD / hour
Experience: At least 7+ years of experience in a Clinical Project Leader III or equivalent senior clinical project leadership role within a contract research organization (CRO).
Posting language: English
Posted: Nov 1, 2026

Original job description

Clinical Project Leader III (Homebased) The Clinical Project Leader serves as a senior clinical trial operations leader responsible for overseeing large, complex Phase II, III, and IV clinical research studies from startup through closeout. This role acts as the primary operational point of contact, ensuring studies remain on schedule, within scope, and compliant with regulatory and protocol requirements. The position focuses heavily on large global cardiovascular and metabolic trials, including diabetes, obesity, and heart disease, and requires extensive collaboration with sponsors, investigators, vendors, and cross-functional internal teams. The Clinical Project Leader provides strategic oversight of site startup, trial execution, risk management, and stakeholder communication while serving as the operational face of the trial to clients and external partners.Responsibilities

Lead the day-to-day operations of Phase II, III, and IV clinical trials from study startup through closeout.
Ensure clinical studies remain on schedule, within scope, and compliant with protocol, Good Clinical Practice (GCP), and applicable regulatory requirements.
Coordinate and align activities between sponsors, sites, investigators, vendors, and internal cross-functional teams.
Identify operational risks, troubleshoot issues, and develop practical solutions to keep projects on track.
Drive study startup activities, including site activation, regulatory submissions, essential document collection, and investigator readiness.
Ensure sites are fully prepared to begin enrollment and conduct study procedures according to protocol and regulatory standards.
Oversee trial progress after startup, maintaining operational oversight and performance monitoring through study completion.
Serve as a primary client-facing contact for sponsors and key study stakeholders throughout the project lifecycle.
Lead study meetings and present clear updates on timelines, enrollment status, risks, and key project milestones.
Build and maintain strong relationships with sponsors, investigators, site personnel, vendors, and internal teams.
Communicate effectively and professionally with internal and external partners, managing expectations and ensuring alignment.
Provide guidance, mentorship, and support to junior Project Leaders and study team members.
Lead cross-functional meetings, ensuring all stakeholders understand priorities, responsibilities, and project objectives.
Contribute to the development and refinement of study processes, workflows, and operational best practices.
Monitor study performance and compliance, addressing operational or quality concerns in a timely and proactive manner.
Support protocol amendments, process improvements, and change management activities as needed.
Ensure adherence to GCP, FDA regulations, and institutional policies across all trial activities.
Manage complex operational logistics associated with multi-country, multi-site global trials.
Oversee and track site startup timelines and milestones, ensuring timely site activation and enrollment readiness.

Essential Skills

At least 7+ years of experience in a Clinical Project Leader III or equivalent senior clinical project leadership role within a contract research organization (CRO).
Bachelors degree (4-year degree) in a relevant field or equivalent education and experience.
Significant clinical trial management experience overseeing complex, multi-site studies.
Proven experience leading Phase II, III, and/or IV clinical trials.
Strong understanding of clinical operations, study conduct, and regulatory requirements, including GCP and FDA regulations.
Demonstrated experience working across multiple functional groups and stakeholders in a matrix environment.
Extensive experience managing large global trials involving multiple countries, international study teams, and global investigators and sites.
Background in cardiovascular and/or metabolic disease clinical research, including areas such as diabetes, obesity, and heart disease.
Expertise in site startup and study activation, including site activation processes, regulatory submissions, essential document collection, and site readiness

Additional Skills & Qualifications

Experience leading large global Phase II/III trials within a CRO environment.
senior Clinical Project Leader Background, ideally at the PL III level.
Strong cardiovascular and metabolic therapeutic area expertise, including experience with diabetes, obesity, and heart disease trials.
Demonstrated ability to serve as the operational face of the trial to sponsors and external partners.
Experience developing and refining study processes, workflows, and operational best practices.
Strong communication, negotiation, and conflict-resolution skills with the ability to escalate and resolve issues professionally.
Proven ability to work independently while contributing to a collaborative team culture.
Preference for candidates located in or able to work effectively within the Eastern Time Zone.
Comfort working in a fast-paced, mission-driven environment with high expectations for quality and performance.
Motivated, go-getter mindset with a willingness to go the extra mile to support the team and project success.

Work EnvironmentThis role offers a 100% remote work environment with a remote-friendly structure that supports flexibility and work-life balance. The position is well-suited for candidates who can work effectively within the Eastern Time Zone, as collaboration with sponsors, investigators, and internal teams may align with that schedule. The work involves extensive use of clinical trial technology platforms and trial management systems to support trial management, site activation, regulatory tracking, clinical operations oversight, and study reporting. You will operate within a mission-driven, collaborative culture that values transparency, inclusion, shared success, and high-quality execution. The environment is fast-paced and high-visibility, providing opportunities to contribute to impactful clinical research while benefiting from training, mentorship, and exposure to diverse therapeutic areas. Job Type & LocationThis is a Contract position based out of Durham, NC. Pay and BenefitsThe pay range for this position is $80.00 - $90.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Durham, NC. Application DeadlineThis position is anticipated to close on Nov 9, 2026. Workplace TypeThis is a fully remote position.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Clinical research
Clinical trials
Google Cloud
Troubleshoot
Regulatory compliance
Change management
Logistics
Research
Communication skills
Negotiation
Conflict resolution
Work independently
Collaboration
Reporting

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