Jobs in the United States

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added 1 min ago
Associate CPLM SME Electrical/ CPLM SME Electrical Engineer - 20678
Northrop Grumman
Roy
Familiarity with working in an AGILE project management environment
Added 1 min ago
Banking Payments Transformation Senior Associate
PWC US
NY-New York, NY · NC-Charlotte, NC · GA-Atlanta, GA · IL-Chicago, IL · DC-Washington, DC
What You Must Have
Added 3 mins ago
Associate, Global Integration & Operations
United Talent Agency
Los Angeles, CA
· 3+ years of experience in operations, project management, business operations, strategy, analytics, consulting, or related roles.
Added 3 mins ago
Senior Associate, Cloud and Platform Security
KPMG LLP
Miami, FL · Orlando, FL · Tallahassee, FL · Tampa, FL
Manage client relationships and project delivery, including workplans, deliverables, status reporting, risk and issue management, and coordination with client, technology, and security…
Added 3 mins ago
Senior Associate, Access Management - Okta & Entra
KPMG LLP
Miami, FL · Orlando, FL · Tallahassee, FL · Tampa, FL
KPMG is currently seeking a Senior Associate, Access Management - Okta & Entra to join our Advisory Services Organization.
Added 3 mins ago
Senior Associate, Identity Governance and Administration (IGA)
KPMG LLP
Miami, FL · Orlando, FL · Tallahassee, FL · Tampa, FL
KPMG is currently seeking a Senior Associate, Identity Governance and Administration to join our Advisory Services Organization.
Added 3 mins ago
Senior Associate, Application Security and Controls - Oracle
KPMG LLP
Miami, FL · Orlando, FL · Tallahassee, FL · Tampa, FL
KPMG is currently seeking a Senior Associate for our Advisory Consulting practice.
Added 3 mins ago
VP, Cloud IAM Engineering Leader
Synchrony Bank
Stamford Engagement Hub, CT · Chicago Engagement Hub, IL · Orlando Engagement Hub, FL · NYC Bryant Park Engagement Hub, NY · Cincinnati West Chester Engagement Hub, OH · Charlotte Engagement Hub, NC · Atlanta Engagement Hub, GA
Lead the design, engineering, testing, deployment, and lifecycle management of IAM access configurations and automation for AWS, Azure, and GCP.
Added 8 mins ago
(=
Associate Director, Access & Reimbursement -Cardiovascular (CV)- St Louis, Missouri
(FCRS = US014) Novartis Pharmaceuticals Corporation
Remote, United States
- $160,300 to $297,700 USD / year
Associate must reside within territory, or within a reasonable daily commuting distance of 60 miles from territory border · Candidate must reside within territory, or within a reasonable daily commuting distance of 60 miles from the territory border
Added 13 mins ago
Research Scientist
Texas A&M University
Houston, TX
…support, behavioral testing, and comprehensive transgenic colony management. The Research Scientist will utilize techniques and strategies taught to them by their education and experiences…
Added 13 mins ago
Postdoctoral Research Associate
Texas A&M University
Houston, TX
The Postdoctoral Research Associate, under general supervision by Dustin Green, is responsible for conducting research in the field of Neuroimmunology. This position supports research…
Added 15 mins ago
Winter Research Associate - Palmer Station / Alternate
LEIDOS, INC.
Remote, United States
Leidos is seeking Winter Research Associate-Alternate to support cutting-edge scientific research at Palmer Station, Antarctica, during the Austral Winter.
Added 16 mins ago
OH
Supervisor Clinical Laboratory
OSF HealthCare
GALESBURG, IL
- $40.11 to $47.19 USD / hour
Associate’s degree in medical laboratory technology, medical laboratory science, or clinical laboratory science AND 4 years' Clinical Laboratory Improvement Act (CLIA) laboratory training…
Added 17 mins ago
Program Officer
James S. McDonnell Foundation
Saint Louis, MO
Strong project management, time management and prioritization skills.
Added 17 mins ago
Associate Program Officer
James S. McDonnell Foundation
Saint Louis, MO
The Associate Program Officer will be an important member of JSMF’s three-person Grants and Impact Investment team, alongside the Director of Grants and Impact Investment and the Program…
Added 18 mins ago
Executive Assistant to Vice President
Northrop Grumman
Baltimore
…capability to take on new and unfamiliar tasks/technologies. Strong project management and multi-tasking skills will be necessary as will emotional intelligence, integrity, and the ability…
Added 19 mins ago
Principal Computer Systems Analyst
Northrop Grumman
Baltimore
Maintain operations of multi-user computer systems working with system engineers, PC desktop technicians, networking engineers, project managers, end users, and IT/Cyber management.
Added 20 mins ago
Manager, Quality Improvement
Humana Insurance Company
FL
Must reside in the state of Florida
Added 23 mins ago
Project Manager, Principal Associate (Social innovation - Mobility Forward Focus)
Capital One
Plano, TX
As a Project Manager, Principal Associate, you will sit at the intersection of Product Management, Project Execution, and Event Leadership. You will be responsible for translating community…
Added 26 mins ago
Colstrip Business Analyst
Talen Montana LLC
Colstrip, MT
Interprets financial, project based, plant process, budget and operational data for discussion with stakeholders to assure the most accurate and efficient financial and business practices…
Added 28 mins ago
Tutor Project-Based
CCRC Child Care Resource Center
United States
Part-time and project-based position: This is an onsite, part-time role typically scheduled during after-school hours, with occasional evening or weekend work based on program needs. This…
Added 31 mins ago
AT
Cook
Archway Transitional Care Center
Macon, GA
- $16.38 USD / hour
Contributes to the work of committees, workgroups, project management, and other collaborative efforts of the System.
Added 32 mins ago
Senior Principal Scientist, Drug Safety
Merck
Rahway, NJ · Upper Gwynedd, PA
…membership on Product Development Teams and chairmanship of the Risk Management and Safety Team, and other related sub-team participation, for assigned products. This may include…
Added 35 mins ago
MD
MATERIAL HANDLER 2
M.C. Dean, Inc
Annapolis Junction, MD
- $25 USD / hour
Must have demonstrated experience and proficiency with intermediate level MS Excel and Outlook
Added 35 mins ago
MD
Material Handler 1
M.C. Dean, Inc
Sterling, VA
- $21 USD / hour
Selected candidates must possess an acceptable driving record in accordance to our policy · Must have demonstrated experience and proficiency with intermediate level MS Excel and Outlook

Actalent

Clinical Research Coordinator

Palo Alto, CA, United States

$30 to $37 USD / hour

Apply on careers.actalentservices.com About employer

Applications open in a new tab.

Job details

Pay: $30 to $37 USD / hour
Experience: Minimum of 1 year of experience as a Clinical Research Coordinator (CRC), Clinical Research Coordinator Associate, or similar role.
Posting language: English
Posted: Nov 10, 2026

Original job description

Job Title: Clinical Research CoordinatorJob DescriptionThis role provides critical administrative and clinical support for the coordination of clinical research studies, with a focus on interventional drug trials. You will work under the close direction and supervision of a principal investigator and/or senior study coordinator, supporting projects from start-up through closeout. The position involves direct interaction with research participants, detailed data collection and management, regulatory documentation, and coordination of study procedures to ensure that all activities follow protocol and regulatory requirements.Responsibilities

Perform administrative support duties related to the collection of clinical data and the coordination of clinical studies under the supervision of the principal investigator and/or study coordinator.
Serve as a primary contact for research participants, sponsors, and regulatory agencies throughout the duration of assigned studies.
Coordinate clinical studies from start-up through closeout, supporting initiation, ongoing conduct, and completion of all study activities.
Schedule and call subjects for study appointments, and contact participants with reminders or other study-related requirements.
Assist with screening, recruiting, and obtaining informed consent from study participants in accordance with study protocols.
Review medical records and conduct telephone or in-person interviews to gather clinical and demographic data as needed.
Prepare, distribute, and process study questionnaires, ensuring timely completion and return by participants.
Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry.
Perform quantitative review of forms, tests, and other measurements for completeness, consistency, and accuracy.
Extract data from source documents for research studies as directed, and accurately collect data to complete case report forms.
Collect and manage patient and laboratory data for clinical research projects, maintaining accurate and up-to-date research project databases.
Develop and maintain study-related documents such as flow sheets, tracking logs, and master subject logs.
Perform clerical duties in the preparation and maintenance of regulatory documents, including consent forms and other required documentation.
Maintain all forms and documents in an organized manner, and file all appropriate study correspondence and records.
Ensure compliance with research protocols, and review and audit case report forms for completeness and accuracy against source documents.
Prepare regulatory submissions as directed and ensure that Institutional Review Board renewals and related regulatory requirements are completed on time.
Coordinate the collection of study specimens according to protocol and ensure proper labeling and documentation.
Prepare, process, and ship specimens and samples accurately under well-defined requirements and timelines.
Perform basic measurements and tests on patients, such as obtaining vital signs, and performing phlebotomy and EKG after appropriate training and certification.
Order and maintain study equipment, supplies, and materials, ensuring that study sites are adequately stocked.
Process study compensation payments and prepare thank-you letters to subjects upon completion of trial activities.
Assist with post-study activities, including data clean-up, document archiving, and study closeout tasks.
Assemble study kits, collect signed consent forms from clinic settings, and perform follow-up data entry and document scanning as needed.
Work on site 34 days per week, collaborating closely with clinical and research staff to support daily study operations.

Essential Skills

Two-year college degree and one year of relevant experience in clinical research or an equivalent combination of education and experience.
Minimum of 1 year of experience as a Clinical Research Coordinator (CRC), Clinical Research Coordinator Associate, or similar role.
Experience with interventional drug studies in a clinical research setting.
Ability to conduct chart reviews and extract relevant clinical information accurately.
Ability to collect, manage, and enter patient and laboratory data for clinical research projects.
Experience with administering and scoring study questionnaires and tests, and coding data for computer entry.
Ability to review forms, tests, and other measurements for completeness and accuracy.
Certifications or active progress toward certification(s) required to perform basic patient measurements and tests, such as phlebotomy and EKG, as applicable.
Ability to coordinate study activities from start-up through closeout under supervision.
Strong organizational skills with the ability to maintain regulatory documents, consent forms, subject logs, and study correspondence.
Ability to ensure compliance with research protocols and assist with auditing case report forms against source documents.

Work EnvironmentThis position operates primarily in a clinical research and office environment, with work performed both in clinical areas and at a desk. The role requires working on site 34 days per week, collaborating closely with investigators, coordinators, and clinical staff. You will regularly use computers for data entry, database management, and preparation of regulatory and study documents. The work involves frequent standing, walking, bending, and interacting with patients, as well as occasional sitting for desk-based tasks such as chart review, documentation, scanning, and telephone calls. You may handle biological specimens, perform or support basic clinical procedures such as vital signs, phlebotomy, and EKG after appropriate training and certification, and prepare and ship samples according to detailed protocols. Job Type & LocationThis is a Contract to Hire position based out of Palo Alto, CA. Pay and BenefitsThe pay range for this position is $30.00 - $37.00/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 to Hire position based out of Palo Alto, CA. Application DeadlineThis position is anticipated to close on Nov 24, 2026. Workplace TypeThis is a hybrid position in Palo Alto,CA.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

Report this job

Work requirements

Jobs in the United States