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Software Technical Program Mgr - Hardware Asset Mg
Kforce
Long Beach, CA
- $80 to $90 USD / hour
Kforce has a client in Long Beach, CA that is seeking an experienced Hardware Asset Management Program Manager to support complex software engineering programs. This individual will partner…
Added just now
Assistant Director of Configuration Management and DevOps Engineering
Federal Home Loan Bank of Atlanta
Atlanta, GA
Manages the implementation and governance of processes related to software release automation, configuration management, environment provisioning, version control, and monitoring. Combines…
Added 1 min ago
CAE Engineer - Early Career Program, Advanced EV
Ford Global
Long Beach, CA
Join us for a 6-month Early Career Program and help build the future of mobility. You'll work alongside top engineering, design, and software talent to create groundbreaking EVs. You'll…
Added 1 min ago
Project Manager-Retail Bank Construction (Ground-Up/Fit-Outs)
Turner & Townsend
Washington D.C., DC
Our capabilities include program, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions.
Added 2 mins ago
Data Scientist, Mid
BOOZ, ALLEN & HAMILTON, INC.
Washington, DC
…and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees…
Added 3 mins ago
Senior Analyst, Global Export Controls
Bose Corporation, U.S.A
MA
…practice and help us lead and support our global export controls program across multiple jurisdictions. This role requires deep technical expertise in export controls regulations, strong…
Added 5 mins ago
Manager, Database Administration
ExactCare Pharmacy, LLC
Remote, United States
The individual will collaborate closely with cross-functional teams including software engineering, data engineering, DevOps, and business stakeholders to deliver high-quality database…
Added 5 mins ago
DevSecOps Cloud Engineer
Trace3
Colorado Springs, CO
Work closely with vendor technical consultants and program engineering teams to deploy cloud environments for development, test and operations.
Added 7 mins ago
Enterprise Cybersecurity Architect
CONCURRENT TECHNOLOGIES CORPORATION
Johnstown, PA
…Serve as the OT-specific Cybersecurity Architect supporting development and deployment of the Marine Corps FRCS Enterprise Architecture. 2. Plan and coordinate a MCEN-hosted FRCS Reference…
Added 7 mins ago
Technical Intern - Cyber Security
Concurrent Technologies Corporation
Johnstown, PA
Current enrollment in an undergraduate degree program in Engineering, MIS/IT, Computer Science, Cybersecurity, or related technical field as a 4th Year/Senior.
Added 7 mins ago
Technical Intern - Cyber Security
CONCURRENT TECHNOLOGIES CORPORATION
Johnstown, PA
Added 7 mins ago
Staff DevOps Engineer
Minitab, LLC
State College, PA
Position Overview Minitab is seeking a highly skilled Staff DevOps Engineer who will support and evolve Minitab's software delivery infrastructure and operational processes. In this…
Added 7 mins ago
Staff DevOps Engineer
Minitab, LLC
State College, PA
…Staff DevOps Engineer who will support and evolve Minitab's software delivery infrastructure and operational processes. In this position, you will lead technical initiatives to optimize…
Added 8 mins ago
Project Manager-Retail Bank Construction (Ground-Up/Fit-Outs)
Turner & Townsend
Philadelphia, PA
Our capabilities include program, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions.
Added 8 mins ago
Finance Portfolio Analytics Analyst
GlaxoSmithKline LLC
Philadelphia, PA
Added 8 mins ago
CI
CDS Intern - Central Engineering UX/UI Designer
Costco IT
Issaquah (Seattle), WA, WA
- $21 to $32.9 USD / hour
…currently enrolled in an IT or related undergraduate or graduate program at a college or university to participate in a 12-week paid internship program during 2027. Interns will work within…
Added 8 mins ago
CI
CDS Intern - Global People Systems-Enhancements & Optimization
Costco IT
Issaquah (Seattle), WA, WA
- $21 to $32.9 USD / hour
…currently enrolled in an IT or related undergraduate or graduate program at a college or university to participate in a 12-week paid internship program during 2027. Interns will work within…
Added 8 mins ago
CI
CDS Intern - Innovation
Costco IT
Issaquah (Seattle), WA, WA
- $21 to $32.9 USD / hour
Dedicated to driving enterprise efficiency and creating future-ready solutions, the Costco Innovation Engineering Team leverages current and emerging technologies. By emphasizing rapid…
Added 8 mins ago
CI
CDS Intern - InfoSec AI/ML
Costco IT
Issaquah (Seattle), WA, WA
- $21 to $32.9 USD / hour
Are you excited by modern AI engineering, building with large language models, agentic systems, and AI-assisted development workflows, while grounding it in strong software fundamentals?…
Added 8 mins ago
Scrum Master
SABEL SYSTEMS TECHNOLOGY SOLUTIONS LLC
Remote, United States
Sabel Systems designs and delivers digital engineering ecosystems for DoD programs, enabling teams to connect data, systems, and personnel within secure, scalable environments. Our…
Added 9 mins ago
Application Developer SME (Containerized Applications Specialist)
Digital Consultants, LLC
Quantico, VA
Candidates must be comfortable applying software engineering principles to disparate languages, operating systems, and hosting environments holistically, learning new technologies as needed…
Added 9 mins ago
Application Developer SME (Artifact Management & Secure Development Specialist)
Digital Consultants, LLC
Quantico, VA
Digital Consultants is seeking an Artifact Management and Secure Software Development Specialist SME Software Engineer for this effort will be responsible for providing guidance and…
Added 9 mins ago
Software Developer-Junior
AMEWAS
Patuxent River, MD
The Guardian Software Development team is responsible for periodic releases of the components that make up the Guardian Software Suite. They will provide safety critical engineering…
Added 11 mins ago
CO
Consulting Engineer (Planning & Project Development) - Austin Energy
City of Austin
United States
- $118,900 to $152,200 USD / year
Develops or oversees development of technical specifications and standards by applying knowledge of the principles and practices of discipline engineering including the methods, materials,…
Added 11 mins ago
CT
Quality Engineer
Creation Technologies International Inc
St. Peter, MN
- $75,000 to $85,000 USD / year
Has primary responsibility for development and maintenance of production quality standards and documentation. Independently cultivate continuous improvement (CI) through problem prevention…

Actalent

Clinical Trial Specialist

New Brunswick, NJ, United States

$35 to $38 USD / hour

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Job details

Pay: $35 to $38 USD / hour
Education: Bachelor’s degree
Posting language: English
Posted: Nov 2, 2026

Original job description

Job Title: Clinical Trial SpecialistJob DescriptionThe Clinical Trial Specialist coordinates and supports all aspects of clinical research studies from initiation through activation and ongoing conduct. This role ensures that protocols meet regulatory and institutional requirements, that participants are properly consented and registered, and that research records are accurate, complete, and audit-ready. The specialist works closely with research nurses, investigators, and study sponsors to maintain compliance with Good Clinical Practice (GCP) guidelines and to advance a broad portfolio of oncology clinical trials.

Responsibilities

Coordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place prior to study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals.
Prepare and organize study tools such as study binders, medication diaries, eligibility checklists, calendars, and flow sheets, tailoring them to the specific requirements of each protocol.
Use clinical trial management systems and Microsoft Excel and Word to develop and maintain study tools, tracking documents, and reports to support efficient study conduct.
In collaboration with the Research Nurse Clinician and/or physician, review patient charts and medical histories to confirm protocol eligibility and obtain all necessary source documents from the medical record.
Under the direction of the Research Nurse Clinician and/or physician, ensure that Institutional Review Boardapproved informed consent forms are properly obtained, signed, filed in the medical record, and that copies are provided to patients.
Register consented research participants with study sponsors, including industry sponsors and cooperative groups, and enter all required information into the clinical trials database.
Maintain complete and accurate research records for all patients enrolled on clinical trials, including consent forms, eligibility documentation, case report forms, registration confirmations, and supporting source documents across multiple centers, community practices, and hospitals.
Assist, in collaboration with the Research Nurse Clinician and physician, with grading adverse events using the most recent National Cancer Institute common toxicity criteria or protocol-specific grading scales.
Complete Serious and Unexpected Adverse Event forms for internal and multicenter events in accordance with study sponsor requirements, federal regulations, and institutional guidelines.
Ensure that research records remain current, organized, and compliant for all assigned patients, supporting monitoring visits, audits, and regulatory inspections.
Use the clinical trials database to generate regular reports for tumor study group members and Principal Investigators on the status of assigned studies and enrolled participants.
Serve as a primary liaison with study sponsors, anticipate sponsor needs, schedule monitoring visits and conference calls, and provide accurate, timely, and well-reasoned responses to sponsor queries.
Work with the Research Nurse Clinician to ensure that investigators and all participating personnel conduct studies according to the protocol treatment plan and Good Clinical Practice guidelines.
Support screening, recruitment, and enrollment of patients to clinical trials, including coordinating study visits and procedures in accordance with protocol requirements.
Communicate clearly and professionally with patients, families, and clinical teams to explain study procedures, answer questions, and facilitate a positive research experience.
Contribute to high enrollment targets across a large portfolio of active trials by efficiently coordinating study activities and helping to identify eligible participants.

Essential Skills

One to three years of relevant clinical research experience, preferably in a clinical research coordinator or similar role.
Experience coordinating clinical research studies, including patient screening, enrollment, and study visit coordination.
Demonstrated experience working with informed consent processes and documentation in a clinical research setting.
Ability to work confidently with source documents and medical records to verify protocol eligibility and support data collection.
Solid knowledge of computer software programs such as Microsoft Excel, Word, and Access.
Comfort and professionalism communicating directly with patients in a clinical or research environment.
Strong attention to detail with the ability to maintain accurate, complete, and organized research records.
Excellent organizational skills with the ability to manage multiple studies and tasks simultaneously.
Clear written and verbal communication skills to interact effectively with investigators, research nurses, sponsors, and other stakeholders.
Strong interpersonal skills to collaborate with multidisciplinary clinical and research teams.
Ability to follow Good Clinical Practice guidelines and institutional policies in day-to-day study conduct.

Additional Skills & Qualifications

Bachelors degree required.
Three or more years of clinical research coordinator experience in oncology is highly beneficial.
Prior experience in oncology clinical trials, including exposure to adverse event grading and NCI toxicity criteria, is a strong plus.
Familiarity with clinical trial management systems and electronic databases for subject tracking and reporting.
Demonstrated ability to hold oneself accountable to high standards of professional excellence and integrity.
Proven ability to maximize available resources, work resourcefully, and adapt to changing priorities in a high-volume research environment.
Commitment to ongoing personal and professional development and to staying current with clinical research best practices.
Strong problem-solving skills and the ability to anticipate and address operational or data-related issues proactively.

Work EnvironmentThis role operates within a large, highly specialized clinical operations and research environment focused on oncology, encompassing disease-specific groups such as breast, lung, phase I, and gastrointestinal studies. The broader research infrastructure includes regulatory affairs, quality assurance, informatics, education, and finance teams, supporting approximately 100 full-time employees. The site manages a robust clinical trial portfolio with around 300 active trials and approximately 1,000 active subjects, with a long-term goal of 2,500 active participants and roughly 5,000 subjects enrolled per year. Studies span all phases and include both adult and pediatric populations. The position supports activity at a major urban campus and multiple satellite sites across the state, requiring coordination across different clinics and hospitals. The work setting is fast-paced and highly collaborative, with significant enrollment demands and frequent interaction with investigators, research nurses, sponsors, and patients. Professional, clinical-appropriate attire is expected, and work is typically conducted during standard business hours, with occasional flexibility needed to meet protocol or sponsor requirements. Job Type & LocationThis is a Contract position based out of New Brunswick, NJ. Pay and BenefitsThe pay range for this position is $35.00 - $38.00/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 New Brunswick, NJ. Application DeadlineThis position is anticipated to close on Nov 16, 2026. Workplace TypeThis is a fully onsite position in New Brunswick,NJ.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
Google Cloud
Clinical trials
Research
Microsoft Excel
Microsoft Word
Documentation
Inspection
Perform studies and field investigation
Microsoft Access
Attention to detail
Organizational skills
Communication skills
Interpersonal skills
Reporting
Problem solving
Regulatory affairs
Quality assurance

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