Jobs in the United States

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Added 1 min ago
Recovery Product Manager
GlaxoSmithKline LLC
Remote, United States
Bachelor’s degree in Technology, Engineering, Business or a related discipline, or equivalent practical experience.
Added 2 mins ago
Project Engineering Intern (Summer 2027)
United States
As a Project Engineering Intern at Collins Aerospace, you will work with a multi-disciplined, technical design and project management team in executing the engineering design process, in a…
Added 2 mins ago
Sr Technician: Drafting/ Product Definition (Onsite)
United States
…position provides an exciting opportunity to contribute to the development of advanced jet engines for both military and commercial programs. You will play a key role in creating and…
Added 3 mins ago
Cloud Security Engineer
PeopleTec, Inc.
HUNTSVILLE, AL
…hybrid, and onsite work arrangements are available, based on program requirements. Occasional travel may be…
Added 3 mins ago
Contracts Manager
Synergy BIS
United States
Synergy Business Innovation & Solutions is a premier implementer of cutting-edge software solutions. Synergy brings the experience and expertise necessary to deliver capability that…
Added 4 mins ago
A
Engineering Project Manager
Actalent
Bingen, WA
- $143,000 to $229,000 USD / year
10+ years combined in product development engineering and engineering project management.
Added 4 mins ago
Mechanical Engineer III
Actalent
Goleta, CA
…an experienced Mechanical Engineer III to lead the design, development, testing, and production transition of advanced electromechanical systems for defense and aerospace applications. In…
Added 4 mins ago
Engineering Intern
Actalent
Valencia, CA
Job Title: Engineering InternJob DescriptionThis Engineering Intern role focuses on performing routine engineering tasks in a manufacturing environment while working closely with…
Added 4 mins ago
A
Software Engineer (C++)
Actalent
Manassas, VA
- $60 to $90 USD / hour
Job Title: C++ Software EngineerJob DescriptionThis role supports a mission-critical submarine acoustic system by focusing on software build, integration, and dependency management across a…
Added 4 mins ago
A
Layout Design Engineer (2D)
Actalent
Pittsburgh, PA
- $65 to $80 USD / hour
…cohesive and efficient layout. The position combines industrial engineering expertise, data-driven analysis, and cross-functional leadership to support large-scale manufacturing growth and…
Added 4 mins ago
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Substation Engineering Supervisor (PE)
Actalent
Charlotte, NC
- $50.07 to $70.1 USD / hour
Job Title: Engineering Supervisor (PE)Job DescriptionThe Engineering Supervisor is responsible for overseeing the daily operations of the department, setting project budgets and schedules,…
Added 4 mins ago
A
Substation Engineering Supervisor (PE)
Actalent
Columbus, OH
- $50.07 to $70.1 USD / hour
Job Title: Engineering Supervisor (PE)Job DescriptionThe Engineering Supervisor is responsible for overseeing the daily operations of the department, setting project budgets and schedules,…
Added 4 mins ago
A
Embedded Software Engineer
Actalent
Loveland, CO
- $40 to $80 USD / hour
Job Title: Embedded Software EngineerJob DescriptionThis role involves contributing to the design and development of embedded firmware solutions for innovative water quality products. The…
Added 4 mins ago
A
Electrical Engineer
Actalent
Loveland, CO
- $48 to $65 USD / hour
Collaborate with cross-functional teams, including mechanical, software, systems, and manufacturing.
Added 4 mins ago
A
Substation Engineering Supervisor (PE)
Actalent
Tulsa, OK
- $50.07 to $70.1 USD / hour
Job Title: Engineering Supervisor (PE)Job DescriptionThe Engineering Supervisor is responsible for overseeing the daily operations of the department, setting project budgets and schedules,…
Added 5 mins ago
Mechanical Engineer
DeBra-Kuempel Inc.
Cincinnati, OH
…of MEP and process piping services, including design-build engineering for new construction and renovation, installation and specialty construction, maintenance, and air balancing,…
Added 8 mins ago
Water & Wastewater Treatment Engineering Intern
Consor Engineers
Knoxville, TN
Career Growth & Development – Tuition reimbursement program, paid professional training, major license achievement bonus, extensive on-demand learning center, and paid professional…
Added 9 mins ago
Lead Data Scientist
PHP Administrative
United States
…prototypes and develop analytical solutions best practices Guide the development of new analytical models to support real time and data driven business decision making. Responsible for…
Added 11 mins ago
Lead Energy Engineer
ICF Resources, LLC
Albuquerque, NM
ICF is growing its energy and distributed energy resource program implementation teams. We are seeking a Lead Energy Engineer to support non-residential transportation electrification,…
Added 12 mins ago
Sr. Full Stack Developer (React/Node)
Omm IT Solutions
Woodlawn, MD
Architect, design, code, and implement next-generation web application using software engineering best practices in the latest technologies: NodeJS, Single Page Application front-end…
Added 15 mins ago
Space Systems Engineer (Senior)
KBR Wyle Services, LLC
Washington, DC
…provides leadership across spacecraft conceptualization, design, development, manufacturing, integration, testing, launch, operations, demonstration, and technical documentation. The…
Added 15 mins ago
Space Systems Engineer (Senior / Sme)
KBR Wyle Services, LLC
Washington, DC
…provides leadership across spacecraft conceptualization, design, development, manufacturing, integration, testing, launch, operations, demonstration, and technical documentation. The…
Added 16 mins ago
Program Analyst (Secret clearance required)
General Dynamics Information Technology
Springfield, VA
Work closely with engineering and cybersecurity teams to ensure program documentation and reporting remain accurate and current.
Added 16 mins ago
PRODUCT OWNER - DIGITAL PLANT
Huntington Ingalls Industries
Newport News, VA
Bachelor’s degree in Business, Computer Science, Engineering, or related field with minimum 0 years of professional experience. • Strong understanding of Agile methodologies.• Excellent…
Added 16 mins ago
ENGINEER SOFTWARE 1
Huntington Ingalls Industries
Newport News, VA
Designs, develops, documents, tests and debugs applications software and systems that contain logical and mathematical solutions. Conducts multidisciplinary research and collaborates with…

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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