Jobs in the United States

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VH
Medical Support Assistant
Veterans Health Administration
Baltimore County, MD · Baltimore, MD
- $53,020 to $68,926 USD / year
Performs various administrative duties as it relates to the Residential Rehabilitation Treatment Program (RRTP) to include admissions and discharges.
Added just now
VH
Senior Social Worker-Primary Care Mental Health Integration (PCMHI)
Veterans Health Administration
Memphis, TN
- $113,708 to $147,824 USD / year
This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific individual eligibility requirements in…
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VH
Advanced Medical Support Assistant
Veterans Health Administration
Middletown, OH
- $51,747 to $67,271 USD / year
Added just now
VH
Senior Licensed Professional Mental Health Counselor-Primary Care Mental Health Integration(PCMHI)
Veterans Health Administration
Memphis, TN
- $89,508 to $116,362 USD / year
This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific eligibility requirements per VHA policy and…
Added just now
VH
Medical Support Assistant
Veterans Health Administration
Baltimore, MD · Baltimore County, MD
- $42,216 to $68,926 USD / year
Performs various administrative duties as it relates to the Residential Rehabilitation Treatment Program (RRTP) to include admissions and discharges.
Added just now
VH
Staff Psychologist Primary Care-Mental Health Integration (PCMHI)
Veterans Health Administration
Millington, TN · Memphis, TN
- $147,890 to $192,259 USD / year
This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific individual eligibility requirements in…
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VH
Registered Nurse - Float Pool (part-time)
Veterans Health Administration
Iron Mountain, MI
- $69,918 to $131,481 USD / year
- Part-time
Position(s) listed under this Open Continuous Announcement (OCA) MAY be eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program.
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VH
Medical Supply Techician (Sterile Processing)
Veterans Health Administration
Erie, PA
- $44,978 to $81,860 USD / year
This position is in the Sterile Processing Services (SPS) program under Patient Care Services at the Erie Veterans Affairs Medical Center. SPS consists of multiple areas, the incumbent of…
Added 1 min ago
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Accounting Supervisor
Jobgether
Remote, United States
- $85,000 to $88,000 USD / year
Cross-Functional Collaboration: Partner with the Accounting Manager, Controller, and other teams to resolve issues, improve processes, and support broader business objectives.
Added 2 mins ago
Director of Nursing
American Senior Communities
WINAMAC, IN
Leadership : Guide, inspire, and support nursing teams to achieve high standards of patient care, drive innovation, and promote a positive and collaborative work environment.
Added 2 mins ago
Documentation Operations Assistant Sr - N2
Lockheed Martin
Lufkin, TX · Lufkin
The Calibration Lab Administrative Aide provides critical administrative and coordination support for the lab’s high-volume calibration operations. This role serves as the primary point of…
Added 2 mins ago
Assistant Contract Manager
MacLellan Integrated Services
Lafayette, IN
Offering a range of services including Critical Process Cleaning, Building & Process Equipment Maintenance, HVAC & Mechanical, Production Support, and Water Treatment Management; MacLellan…
Added 3 mins ago
Cybersecurity Engineer (Cloud)
Amentum
Indianapolis, IN
Administer assigned cloud security posture management and workload protection capabilities, including environment onboarding, policy configuration, security recommendations, coverage…
Added 3 mins ago
VH
Advanced Practice Nurse - Certified Nurse Anesthetist
Veterans Health Administration
Washington, DC
- $180,195 to $261,224 USD / year
This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific eligibility requirements per VHA policy and…
Added 3 mins ago
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Program Manager (Deputy Site Manager)
Other Agencies and Independent Organizations
Plainsboro, NJ
- $174,347 to $197,200 USD / year
Operations & Program Management: Serve as alter ego to the Site Manager by exercising line management authority over site operations, strategic and operational planning, projects, budget…
Added 3 mins ago
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Training Administrator
Executive Director, Office of Acquisition, Logistics and Construction
Frederick, MD · Washington, DC
- $143,913 to $187,093 USD / year
…The incumbent serves as the Director of Operations for the Program Management School under the direct supervision of the Vice Chancellor. The selectee works independently and closely with…
Added 3 mins ago
VH
Diagnostic Radiologic Technologist (MRI)
Veterans Health Administration
North Chicago, IL
- $79,170 to $102,926 USD / year
…equivalent) in a post-high school diagnostic radiologic technology program, evidenced by a certificate or an associate's degree, accredited by the Joint Review Committee on Education in…
Added 3 mins ago
VH
Registered Nurse - Home Based Primary Care
Veterans Health Administration
Jefferson Barracks, MO
- $75,487 to $153,842 USD / year
…within the interdisciplinary team, and fosters a professional environment that supports learning and growth. The nurse provides constructive feedback, advocates for high-quality patient…
Added 3 mins ago
VH
Senior Social Worker
Veterans Health Administration
Baton Rouge, LA
- $93,514 to $121,571 USD / year
…care tools, semi-annual treatment plans for all Veterans and program evaluation forms sent to the Northeast Program Evaluation Center (NEPEC). S(he) will be responsible for completion of…
Added 3 mins ago
VH
Senior Social Worker
Veterans Health Administration
Augusta, GA
- $92,903 to $120,776 USD / year
…part of the Mental Health Residential Rehabilitation Treatment Program (MH RRTP). The Senior Social Worker operates as a clinical mental health provider, serving as a key member of an…
Added 3 mins ago
VH
Medical Supply Technician (Sterile Processing)-Trainer
Veterans Health Administration
Aurora, CO
- $64,228 to $83,498 USD / year
…assembly, sterilization, scope reprocessing and distribution of critical and semi-critical Reusable Medical Device (RMD) throughout medical center and Community Based Outpatient Clinics…
Added 3 mins ago
VH
Senior Licensed Professional Mental Health Counselor
Veterans Health Administration
Augusta, GA
- $89,508 to $116,362 USD / year
…Veterans in the Mental Health Residential Rehabilitation Treatment Program (MH RRTP). Duties include comprehensive assessments, individual and group psychotherapy, treatment planning,…
Added 3 mins ago
VH
Healthcare Engineer
Veterans Health Administration
Salem, VA
- $62,849 to $139,563 USD / year
The position serves as resident and program engineer consisting of the planning, design, and overseeing of major healthcare system projects; oversees Professional Architecture/Engineering…
Added 3 mins ago
VH
Medical Support Assistant (Advanced)
Veterans Health Administration
Murfreesboro, TN
- $50,168 to $65,219 USD / year
…deemed at least equivalent to that gained in a conventional U.S. program by a private organization specializing in the interpretation of foreign educational…
Added 4 mins ago
Multifunctional Manufacturing Planner Sr Mgr - L6
Lockheed Martin
Orlando, FL · Orlando
Support multiple program needs to achieve critical schedule milestones by navigating competing priorities and maintaining momentum

Actalent

Sr CRA I

Santa Clara, CA, United States

$58.62 to $62.07 USD / hour

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Job details

Pay: $58.62 to $62.07 USD / hour
Experience: Previous experience that provides the knowledge, skills, and abilities to perform the role, comparable to at least 2 years of experience as a clinical research monitor.
Posting language: English
Posted: Nov 2, 2026

Original job description

6 month contract - renewable or conversion to PERM after 6 monthsPaid for all hours (travel included) - door to doorBenefits included (w2 only)Job Title: Senior Clinical Research Associate I (Sr CRA I)Job DescriptionThe Senior Clinical Research Associate I performs and coordinates all aspects of clinical monitoring and site management for diverse clinical trials. This role conducts remote and on-site monitoring visits to assess protocol and regulatory compliance, ensures high-quality documentation, and supports trials across multiple sponsor models and monitoring environments. The Sr CRA I acts as a site process specialist, ensuring that studies are conducted in accordance with approved protocols, ICH-GCP guidelines, applicable regulations, and standard operating procedures to safeguard participant rights, well-being, and data integrity. The position emphasizes audit readiness, strong collaboration with investigational sites, and effective communication with project teams in a dynamic, global clinical research environment.Responsibilities

Perform comprehensive clinical monitoring and site management activities for assigned clinical trials, both remotely and on-site.
Monitor investigator sites using a risk-based monitoring approach, applying root cause analysis, critical thinking, and problem-solving to identify site process failures and implement corrective and preventive actions.
Ensure data accuracy and integrity through source data review (SDR), source data verification (SDV), and case report form (CRF) review during on-site and remote monitoring activities.
Assess investigational product accountability through physical inventory checks and records review, ensuring compliance with protocol and regulatory requirements.
Document monitoring observations in clear, timely reports and correspondence using approved business writing standards, and ensure all documentation meets audit readiness expectations.
Escalate site deficiencies, risks, and issues promptly to clinical management and follow all findings through to full resolution in collaboration with project team members.
Maintain regular contact with investigational sites between monitoring visits, as needed, to confirm protocol adherence, verify resolution of previously identified issues, and support timely and accurate data entry.
Conduct monitoring tasks in strict accordance with the approved monitoring plan and study-specific procedures.
Participate in the investigator payment process, ensuring accurate tracking and appropriate follow-up on payment-related matters.
Share responsibility with project team members for issue and finding resolution, investigating and following up on site-related concerns as applicable.
Provide trial status tracking and progress updates to the Clinical Team Manager and update study systems, including Clinical Trial Management Systems (CTMS), according to agreed study conventions.
Perform quality control checks of reports generated from CTMS or other study systems when required to ensure data accuracy and completeness.
Participate in investigator meetings as needed, supporting site training, protocol clarification, and study start-up activities.
Identify potential investigators in collaboration with sponsor teams to evaluate and recommend qualified investigational sites.
Initiate clinical trial sites according to relevant procedures, ensuring compliance with the protocol, regulatory requirements, and ICH-GCP obligations, and make recommendations where warranted.
Ensure proper trial close-out at assigned sites, including retrieval of trial materials and confirmation that essential activities are completed.
Verify that required essential documents are complete, current, and appropriately filed in accordance with ICH-GCP and applicable regulations.
Conduct on-site file reviews as specified in project requirements to ensure documentation quality and regulatory compliance.
Contribute to project teams by assisting in the preparation of project publications, tools, and communications, and by sharing ideas and suggestions for improved processes.
Perform additional study-related tasks as assigned by clinical leadership, such as reviewing trip reports, creating newsletters, and leading CRA team calls to support study oversight.
Facilitate effective communication between investigative sites, sponsor representatives, and the project team through clear written, oral, and electronic correspondence.
Respond to company, sponsor, and regulatory requirements, including audits and inspections, by providing accurate information and supporting corrective actions as needed.
Complete administrative tasks such as expense reports and timesheets accurately and on time.
Contribute to other project work and continuous process improvement initiatives as required, supporting operational excellence across studies.

Essential Skills

Bachelor's 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 of experience as a clinical research monitor.
Valid driver's license where applicable to support required travel.
Effective clinical monitoring skills, including on-site and remote monitoring of investigational sites.
Demonstrated understanding of medical and therapeutic area concepts and medical terminology, including experience in clinical research, oncology, and CNS studies.
Excellent understanding and practical application of ICH-GCP guidelines, applicable regulations, and procedural documents.
Strong critical thinking abilities, including an investigative mindset, thorough root cause analysis, and effective problem-solving skills.
Ability to manage and apply risk-based monitoring concepts and processes in day-to-day monitoring activities.
Effective oral and written communication skills, with the ability to communicate clearly and professionally with medical personnel and project stakeholders.
Strong attention to detail, ensuring accuracy in documentation, data review, and reporting.
Effective organizational and time management skills, with the ability to prioritize tasks and manage multiple responsibilities.
Ability to remain flexible and adaptable across a wide range of scenarios, studies, and monitoring environments.
Ability to work both independently and as part of a collaborative project team.
Good computer skills, including proficient use of Microsoft Office applications and the ability to learn and use clinical trial software systems such as CTMS.
Strong English language and grammar skills, supporting high-quality written reports and presentations.
Good presentation skills, enabling effective participation in investigator meetings and team discussions.

Additional Skills & Qualifications

Experience working with different sponsor models and monitoring environments, including functional service organizations (FSO), functional service providers (FSP), and government-sponsored studies.
Familiarity with clinical research processes in global contract research organizations and exposure to diverse therapeutic areas.
Ability to build and maintain collaborative relationships with investigational sites and project team members.
Experience contributing to project tools and publications, such as newsletters and study-related communications.
Capability to lead or support CRA team calls and contribute to team coordination efforts.
Demonstrated customer focus, including strong listening skills, attention to detail, and the ability to recognize and address underlying site and sponsor needs.
Willingness to engage in continuous learning and process improvement initiatives to enhance study quality and efficiency.
In some cases, a combination of appropriate education, training, and directly related experience may be considered equivalent to formal degree requirements.

Work EnvironmentThis position is 100% home-based, offering the flexibility to work remotely while supporting clinical trials across multiple regions. The role requires significant travel, with an estimated 6080% travel commitment and an average of 810 overnight monitoring visits per month to investigational sites. Work is conducted using standard office technology, including Microsoft Office and clinical trial management systems, in a professional environment focused on collaboration, regulatory compliance, and high-quality data. The culture emphasizes partnership with leading pharmaceutical and biotechnology organizations, exposure to diverse therapeutic areas, and participation in a global clinical research setting.#ActTFjobs26 Job Type & LocationThis is a Contract position based out of Santa Clara, CA. Pay and BenefitsThe pay range for this position is $58.62 - $62.07/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 Santa Clara, CA. Application DeadlineThis position is anticipated to close on Nov 6, 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
Root cause analysis
Critical thinking
Problem solving
Monitor activities
Regulatory compliance
Documentation
Data entry
Quality control
Leadership
Communication skills
Inspection
Process improvement
Valid driver's licence
Medical terminology
Attention to detail
Reporting
Time management
Prioritization
Adaptability
Computer skills
Microsoft Office
Presentation skills
Research
Collaboration
Biotechnology

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