Jobs in the United States

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ENG Tech (WLD)
AVMAC LLC
Chesapeake, VA
Report job status, discrepancies, and material requirements to the Lead or Program/Project Manager (PM) in a timely manner.
Added just now
ENG Tech (ELE)
AVMAC LLC
Chesapeake, VA
Report job status, discrepancies, and material requirements to the Lead or Program/Project Manager (PM) in a timely manner.
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Global Workplace Experience & Strategy Director
Nokia
United States
Based in Dallas with a global remit, you will lead Workplace Strategy within Nokia’s Real Estate Strategy & Portfolio team. You will partner with HR, IT, Area Management, Portfolio…
Added 1 min ago
Account Lead
JLL
Seattle, WA
The Account Lead serves as the on-site leader for a major corporate account within JLL Work Dynamics. This is a program-builder role: you will establish the foundational SOPs, governance…
Added 1 min ago
CO
Water Division Manager
City of South Gate
South Gate, CA
- $63.77 to $77.52 USD / hour
Knowledge of: administrative principles and practices including goal setting, program development, implementation, and evaluation, and project management; principles and practices of budget…
Added 1 min ago
Head of Program Management, DoorDash Air
DoorDash USA
San Francisco, CA
We're hiring a Head of Program Management for DoorDash Air, our in-house drone delivery program. DoorDash Air is an FAA Part 135 certified air carrier, flying aircraft we design and build…
Added 1 min ago
Senior Client Advocate
WTW
Radnor, PA
Insurance P&C License required
Added 2 mins ago
Grants/Contracts Coordinator
Oregon Health & Science University
Beaverton, OR
Experience in an administrative support or project management role for faculty or upper-level management.
Added 2 mins ago
Senior Substation Engineer - P&C - Power Delivery
WESTWOOD PROFESSIONAL SERVICES INC
Overland Park, KS
Lead the development and finalization of protection and control specifications, device applications, and related material documentation, ensuring compliance with project and client…
Added 2 mins ago
Senior Substation Engineer - P&C - Power Delivery
WESTWOOD PROFESSIONAL SERVICES INC
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Lead the development and finalization of protection and control specifications, device applications, and related material documentation, ensuring compliance with project and client…
Added 2 mins ago
Senior Substation Engineer - P&C - Power Delivery
WESTWOOD PROFESSIONAL SERVICES INC
Lansdale, PA
Lead the development and finalization of protection and control specifications, device applications, and related material documentation, ensuring compliance with project and client…
Added 2 mins ago
Power Generation Project Engineer, Associate (Mechanical)
Pacific Gas And Electric Company
Angels Camp, CA
This Associate Level Project Engineer position is the first in a progression. This job provides engineering, project management, and technical support to O&M staff, for small to medium…
Added 2 mins ago
Senior Substation Project Engineer
Pacific Gas And Electric Company
Oakland, CA
…Electric Operations partners. Our organization is accountable for program planning, financial budgeting, and project execution and delivery of all electric engineering projects. Electric…
Added 2 mins ago
Project Executive
Gilbane Building Company
Cleveland, OH
…team environment on complex projects? Gilbane is seeking a Project Executive to lead a single large project team or multiple small project teams, guiding the overall direction, completion,…
Added 3 mins ago
Project Manager- Agile
Endava
Remote, United States
We are looking for a seasoned technical Project Manager and Scrum Master to lead end-to-end delivery of two strategic initiatives: SpendIQ, our AI-powered Supplier Spend Intelligence…
Added 3 mins ago
Manager - Compass
Expand Energy
Oklahoma City, OK
Coordinate with sales, estimating, project management, and engineering on order intake, contract and scope review, lead times, shop capacity, and change orders so commitments made to…
Added 3 mins ago
Reliability Systems Specialist
Carlisle
Carlisle, Pennsylvania, PA
Carlisle is seeking a Reliability Systems Specialist to lead the implementation and optimization of our Computerized Maintenance Management System (CMMS) and align maintenance operations…
Added 4 mins ago
Mgr, ESG Data & Reporting
Bath & Body Works
Columbus, OH
Bath & Body Works is seeking a Manager, ESG Data & Reporting to play a critical role in advancing how we lead, measure and report ESG data across the enterprise! This role leads ESG data…
Added 4 mins ago
Director of Technical Operations
AmerisourceBergen Services Corporation
Remote, United States
…with Software Engineering, Infrastructure/Cloud, Security, and Program/Project leadership to ensure reliable production operations, strong incident management practices, post-launch…
Added 4 mins ago
Senior Manager, Program Management Office
Hill Phoenix, Inc.
Conyers, GA · Atlanta, GA
We are looking for experienced senior manager to lead our program management office (PMO) team. PMO drives new product introductions, design to value, complexity reduction and sustaining…
Added 4 mins ago
ASQ Quality Manager
Ace Electric
VALDOSTA, GA
The Quality Manager will lead the implementation and ongoing management of an ISO 9001-certified Quality Management System, develop and maintain quality policies and procedures, oversee…
Added 4 mins ago
Engineering Manager
Bechtel Corporation
United States
Several major capital program projects are currently planned to be developed and executed by Bechtel over the next 5-10 years. During the development phase of these projects, teams will be…
Added 4 mins ago
Associate Analytics Manager
Molson Coors
Chicago
You will lead the development and execution of custom analyses and conduct quality checks to ensure validity
Added 5 mins ago
Senior Analyst – Strategic Accounting Initiatives, Corporate Accounting
Acrisure, LLC
GRAND RAPIDS, MI
…collaborate across functions to support ongoing strategic projects, lead defined project workstreams, and independently own smaller initiatives from planning through completion. The…
Added 5 mins ago
Regional Sale Manager
Hearst
Remote, United States
Build a robust opportunity funnel by organic (cold calling) and coordinated efforts with Zynx Account and Project Management teams as well as a third party lead generation firm

Actalent

Sr CRA II

Kansas City, MO, United States

$70 to $95 USD / hour

Apply on careers.actalentservices.com About employer

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Job details

Pay: $70 to $95 USD / hour
Posting language: English
Posted: Nov 12, 2026

Original job description

Job Title: Clinical Research Associate (CRA) Central or West RegionJob DescriptionThis role performs and coordinates all aspects of clinical monitoring and site management for sponsored clinical trials. You will conduct remote and on-site monitoring visits to assess protocol and regulatory compliance, manage essential documentation, and ensure that studies are conducted in accordance with ICH-GCP guidelines, applicable regulations, and internal standard operating procedures. As a site process specialist, you will help safeguard participant rights and well-being, support data accuracy and reliability, and maintain audit readiness while building strong, collaborative relationships with investigational sites.Responsibilities

Perform comprehensive clinical monitoring and site management activities for assigned clinical trials, both remotely and on-site.
Conduct monitoring visits using a risk-based monitoring approach, applying root cause analysis, critical thinking, and problem-solving skills to identify site process failures and define corrective and preventive actions.
Ensure data accuracy and integrity through source data review (SDR), source data verification (SDV), and case report form (CRF) review, in line with the approved monitoring plan.
Assess investigational products through physical inventory checks and review of related records to confirm proper handling and accountability.
Document all observations, findings, and follow-up actions in monitoring reports and correspondence using approved business writing standards and submit these in a timely manner.
Escalate site deficiencies, non-compliance issues, and risks to clinical management promptly and track all issues through to resolution in collaboration with the project team.
Maintain regular contact with investigative sites between monitoring visits to confirm protocol adherence, verify resolution of previously identified issues, and ensure timely and accurate data entry.
Participate in the investigator payment process in accordance with study procedures and sponsor requirements.
Provide trial status tracking and progress updates to the Clinical Team Manager (CTM) or project leadership as required.
Update study systems, including the Clinical Trial Management System (CTMS), following agreed study conventions and perform quality control checks of system-generated reports when needed.
Participate in investigator meetings as required, supporting site engagement and study start-up activities.
Collaborate in identifying potential investigators and evaluating site suitability to ensure the acceptability of qualified investigative sites.
Initiate clinical trial sites following relevant procedures to ensure compliance with the protocol, regulatory requirements, and ICH-GCP obligations, making recommendations when appropriate.
Ensure trial close-out activities are completed, including retrieval of trial materials and confirmation that essential documentation is finalized and filed.
Verify that required essential documents are complete, accurate, and maintained in accordance with ICH-GCP and applicable regulations, including conducting on-site file reviews as specified by the project.
Contribute to project deliverables by assisting in the preparation of study publications, tools, newsletters, and other project-related materials.
Lead or participate in CRA team calls when assigned, and facilitate effective communication between investigative sites, the sponsor, and the broader project team through written, oral, and electronic channels.
Respond to company, sponsor, and regulatory requirements, including audits and inspections, by providing documentation and information and supporting corrective actions.
Complete administrative tasks such as expense reports and timesheets accurately and within required timelines.
Support other project work and process improvement initiatives as needed, sharing ideas and best practices with colleagues.

Essential Skills

Bachelors degree in a life sciences-related field, a Registered Nursing certification, or an equivalent and relevant formal academic or vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the role, comparable to at least 2+ years as a clinical research monitor or Clinical Research Associate.
Valid drivers license where applicable to support required travel.
Effective clinical monitoring skills, including experience conducting remote and on-site visits and managing essential trial documentation.
Strong understanding of medical and therapeutic areas and proficiency with medical terminology.
Excellent knowledge and practical application of ICH-GCP guidelines, applicable regulations, and procedural documents.
Well-developed critical thinking skills, including the ability to perform in-depth investigations, conduct root cause analysis, and implement appropriate problem-solving strategies.
Ability to manage and apply Risk Based Monitoring concepts and processes in daily monitoring activities.
Effective oral and written communication skills, with the ability to communicate clearly and professionally with medical and clinical personnel.
Strong attention to detail and accuracy in reviewing data, documentation, and reports.
Effective organizational and time management skills, with the ability to prioritize tasks and meet deadlines.
Ability to remain flexible and adaptable across a wide range of study scenarios and changing priorities.
Ability to work both independently with minimal supervision and collaboratively within cross-functional teams.
Proficient computer skills, including strong knowledge of Microsoft Office and the ability to learn and use clinical trial-related software and systems such as CTMS.
Good command of the English language, including grammar, for professional communication and report writing.
Confident presentation skills for investigator meetings and internal team discussions.

Additional Skills & Qualifications

Experience working within different sponsor models or monitoring environments, such as functional service provider (FSO/FSP) arrangements and government-sponsored studies.
Familiarity with Trial Master File (TMF) requirements and documentation practices.
Experience with risk-based monitoring methodologies and tools.
Background in a global contract research or clinical research organization environment.
Ability to maintain strong customer focus through attentive listening, attention to detail, and the ability to understand and address underlying site and sponsor needs.
Strong interpersonal skills that support effective collaboration with site staff, project teams, and stakeholders.
Experience contributing to project publications, tools, newsletters, and other study-related communications.
Experience participating in or supporting audits and inspections, including preparation of documentation and responses.
Equivalency of education, training, and directly related experience may be considered in lieu of formal degree requirements.

Work EnvironmentThis is a 100% home-based position within the United States, offering flexibility to work from your home office while supporting clinical trial sites across the West region. The role requires frequent travel, typically in the range of 6080%, for on-site monitoring visits, site initiation, close-out activities, and investigator meetings. You will use standard office technology, including a computer with Microsoft Office and clinical trial systems such as CTMS, along with secure electronic communication tools to collaborate with sites and project teams. Travel may involve varying schedules depending on study needs, and you will work within a professional, process-driven environment focused on regulatory compliance, data quality, and continuous improvement. Job Type & LocationThis is a Contract position based out of Kansas City, MO. Pay and BenefitsThe pay range for this position is $70.00 - $95.00/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 Kansas City, MO. Application DeadlineThis position is anticipated to close on Nov 20, 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.

Apply on careers.actalentservices.com About employer

More about this job

Skills

Clinical research
Clinical trials
Regulatory compliance
Documentation
Google Cloud
Root cause analysis
Critical thinking
Problem solving
Data entry
Leadership
Quality control
Communication skills
Inspection
Process improvement
Medical terminology
Monitor activities
Attention to detail
Time management
Prioritization
Meet deadlines
Adaptability
Computer skills
Microsoft Office
Report writing
Presentation skills
Research
Interpersonal skills
Collaboration
Electronic communication

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Work requirements

Jobs in the United States