Jobs in the United States

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added 1 min ago
Senior Consultant- Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 1 min ago
Senior Consultant - Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 1 min ago
Senior Consultant - Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 1 min ago
DiGeronimo Companies
DiGeronimo Companies
Atlanta, GA · Cleveland, OH · Pittsburgh, PA · Charlotte, NC · Dallas, TX
Must have strong organizational skills in order to handle the varieties of tasks assigned
Added 1 min ago
Director, Avendra Supply Chain
Aramark
Philadelphia, PA
Project management experience with successful execution of complex initiatives.
Added 1 min ago
Senior Consultant - Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 1 min ago
Senior Consultant - Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 1 min ago
Senior Consultant - Pharmacy Business Manager
Vizient, Inc.
United States
…client pharmacy leaders to develop innovative solutions, guide project execution, interpret complex financial and operational data, and present actionable insights to senior leadership. You…
Added 2 mins ago
TF
Research, Evaluation & Learning Manager
The Food Bank of Northern Nevada Inc
Sparks, NV
- $75,649.6 to $80,155.2 USD / year
…Northern Nevada's efforts to understand community needs, evaluate program effectiveness, measure community impact, and translate research and evaluation findings into actionable insights…
Added 2 mins ago
Channel Program Manager
DLT Solutions, LLC
Greenville, SC
3+ years of experience in program management, project management, partner management, operations, customer success, vendor management, onboarding, or a related field.
Added 3 mins ago
Senior Intel Analyst
SAIC
Point Mugu Nawc, CA · Point Mugu NAWC, CA
SAIC is looking for a Senior Intelligence Analyst to support the Electronic Warfare Data Systems (EWDS) program for the Airborne Electronic Attack Integrated Product Team (AEA IPT) located…
Added 3 mins ago
Sr Program Management Specialist
RocketForce Technologies LLC
Mason, OH
Job Description: Senior Program Manager Specialist
Added 4 mins ago
IL
Senior Associate, Community Engagement
Invenergy LLC
Denver, CO
- $98,000 to $125,000 USD / year
As Senior Associate, Community Affairs, you will lead local outreach and serve as a key relationship contact for county/municipal officials, local taxing bodies, chambers, and Economic…
Added 5 mins ago
SL
Plant Manager
STIMSON LUMBER COMPANY
St Maries, ID
- $175,000 to $195,000 USD / year
Proven experience in plant management or senior manufacturing leadership, with a strong track record in maintenance supervision and program development.
Added 6 mins ago
Director, Transportation Safety & Compliance (USFS) - South Market - USBL
Sysco Payroll, Division of Sysco Resources Services, LLC
Remote, United States
Excellent analytical skills and interpersonal skills, ability to interact effectively with all levels of senior management, supervision and employees.
Added 6 mins ago
Senior Human Resources Business Partner
Children's Hospital
United States
Strong project management and prioritization skills.
Added 6 mins ago
Senior REMS Compliance Auditor - Supervisor
United Biosource Corporation
Remote, United States
UBC is seeking an experienced Senior REMS Compliance Auditor with management experience to oversee REMS Auditors.
Added 6 mins ago
C
Sr Project Manager-Transmission & Substation
ComEd
OAKBROOK TERRACE, IL
- $100,800 USD / year
The Sr Project Manager is an individual contributor accountable for project budgets, team performance and developing strategic plans to implement projects for various organizations.…
Added 7 mins ago
Senior Executive Administrative Assistant
Olympus Corporation of the Americas
Center Valley, PA
Must have a global mind set; time zone management
Added 7 mins ago
Zero Trust Communication & Liaison SME
Pueo Business Solutions LLC
Mclean, VA
…stakeholder engagement lead supporting the CIO’s Zero Trust Program. Operating at the intersection of deep cybersecurity architecture and executive-level strategic messaging, this role…
Added 8 mins ago
Senior Geomechanical Engineer
Freeport McMoRan
Bayard, NM
Employees may be required to work a non-standard schedule, which may include shift work (other than day shift) at a 24/7, 365-day operation
Added 9 mins ago
Senior Commercial Banking Portfolio Manager
B10 Wells Fargo Bank, N. A.
IRVINE, CA · FRESNO, CA · WEST COVINA, CA · PORTLAND, OR · SALT LAKE CITY, UT · SAN DIEGO, CA · LOS ANGELES, CA · BELLEVUE, WA
Resolve moderately complex issues and lead Commercial Banking Portfolio Management team, to meet project deliverables, while leveraging solid understanding of the function, policies,…
Added 9 mins ago
O
Lead Principal Data Center Cost Manager
Oracle
Jefferson City, MO
- $126,200 to $264,100 USD / year
The ideal candidate will have a strong background in cost control, contract administration, and risk management within the data center or critical infrastructure sector. Responsibilities…
Added 10 mins ago
Clinical Workflow Lead, Home Therapies
Fresenius Medical Care
Remote, United States
· Provides senior level project management and team facilitation support to process improvement and utilizes the project life-cycle to plan, implement, monitor and sustain associated…
Added 10 mins ago
Clinical Workflow Lead, In-Center HD
Fresenius Medical Care
Remote, United States
Provides senior level project management and team facilitation support to process improvement and utilizes the project life-cycle to plan, implement, monitor and sustain associated…

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