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BTIG: Research, Equity Research Associate, Analyst (Chemicals)
U.S. Bank National Association
New York, NY
BTIG seeks an Associate to support the Equity Research team in the Chemicals and Electronic Materials space. This individual will be responsible for assisting a Senior Analyst in covering…
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PCS Finance Director
U.S. Bank National Association
Minneapolis, MN
Demonstrated experience leading complex financial planning, forecasting, performance management, and strategic decision support.
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Culinary Supervisor
Crescent Hotels & Resorts
Horseshoe Bay, TX
Recipe Adherence: Execute and enforce strict adherence to standardized recipes and portion control to ensure consistency and cost management.
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Preschool and School Age Associate Teacher
Catalyst Family Inc.
Fillmore, CA
Catalyst teaching staff support the planning and implementation of Catalyst's programming for children ranging in age from infant, toddler, pre-school, kinder, and school age depending on…
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2027 Sales Internship - Tempe
CDW, LLC
Tempe, AZ
- $19 USD / hour
Are you ready to launch your sales career? Join CDW’s Summer Sales Internship Program and gain hands-on experience in business-to-business technology sales. Work alongside top-performing…
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CL
2027 Sales Internship - Chicago
CDW, LLC
Chicago / Adams, IL
- $19 USD / hour
Are you ready to launch your sales career? Join CDW’s Summer Sales Internship Program and gain hands-on experience in business-to-business technology sales. Work alongside top-performing…
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CL
2027 Sales Internship - Dallas
CDW, LLC
Dallas, TX
- $19 USD / hour
Are you ready to launch your sales career? Join CDW’s Summer Sales Internship Program and gain hands-on experience in business-to-business technology sales. Work alongside top-performing…
Added just now
CL
2027 Sales Internship - Cherry Hill
CDW, LLC
Cherry Hill, NJ
- $19 USD / hour
Are you ready to launch your sales career? Join CDW’s Summer Sales Internship Program and gain hands-on experience in business-to-business technology sales. Work alongside top-performing…
Added 1 min ago
Program Supervisor - CBEP
The New York Foundling
New York, NY
Track team data and complete progress monitoring reports to maintain accurate data tracking and reporting to support strategic planning and improve program performance and accountability.
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Education Manager
Neighborhood House
Portland, OR
In support of the Agency’s mission, the Education & Development Services Manager is responsible for ensuring the provision of high quality comprehensive early childhood services by leading,…
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Employee Relations Specialist
SupplyHouse.com
Remote, United States
- $73,655 to $110,482 USD / year
Confidential mental health, financial planning, and legal support through our Employee Assistance Program (EAP)
Added 1 min ago
A
Senior Solution Architect
Akur8
New York City, NY · Chicago, IL · Boston, MA · Atlanta, GA
- $275,000 to $325,000 USD / year
- Own the technical outcome of complex Deploy engagements, or defined workstreams inside a larger program, from discovery through production, with the customer's team doing the build.
Added 1 min ago
Maintenance & Reliability Manager
Precision Associates Inc.
Minneapolis, MN
Prioritize resources to support business needs.
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2027 Engineering Internship
Horwitz
New Hope, MN
Support project management on various projects by preparing O&M manuals, performing Revit modeling, and conducting load calculations.
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Program Assistant
New York Housing Trust Fund
New York, NY
The Program Assistant for Small and Mid-Size Development will work closely with SMD’s Vice President, Assistant Vice President, and program staff to support day-to-day implementation of…
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Room Attendant
the goodtime hotel
Miami Beach, FL
Highgate is a leading real estate investment and hospitality management company with over $15 billion of assets under management and a global portfolio of more than 400 hotels spanning…
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Temporary HR Director
Monterey Beach Hotel
Monterey, CA
Highgate is a leading real estate investment and hospitality management company with over $15 billion of assets under management and a global portfolio of more than 400 hotels spanning…
Added 1 min ago
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OPS GOVERNMENT OPERATIONS CONS II - 37970060
State of Florida
TALLAHASSEE, FL
- $25 to $27 USD / hour
The business systems and process improvement analyst will create tools to gather, organize, and distribute data that is generated and used by the office and other program areas.
Added 1 min ago
SO
MEDICAID WAIVER LIAISON - 67014883
State of Florida
FT MYERS, FL
- $38,264.07 to $55,001.96 USD / year
…reviews for individuals served through the Medicaid waiver program, processing cost plan amendment requests for changes in Medicaid waiver services, processing requests for changes in…
Added 1 min ago
Property & Accountability Specialist
State of Florida
EAST PALATKA, FL · FLEMING ISLAND, FL · GREEN COVE SPRINGS, FL · HASTINGS, FL · JACKSONVILLE, FL · MIDDLEBURG, FL · ORANGE PARK, FL · PALM COAST, FL · SAINT AUGUSTINE, FL · ST AUGUSTINE, FL
The mission of the Florida Department of Military Affairs is to provide management oversight of the Florida National Guard and provide units and personnel ready to support national security…
Added 1 min ago
MC
Senior Learning & Development Partner
Michels Corporation
Otsego, MN · Madison, WI
- $94,000 to $129,000 USD / year
…of employees along with supporting learning and development program initiatives. The Senior Learning and Development Partner is responsible for supporting multiple Business Operations areas…
Added 1 min ago
SO
SENIOR ADULT PROTECTIVE INVESTIGATOR - 60021100
State of Florida
STUART, FL
- $41,000.18 USD / year
…class. The omission of specific statements does not preclude management from assigning specific duties not listed herein if such duties are a logical assignment to the…
Added 1 min ago
SENIOR COMMUNITY HEALTH NURSE - 64000748
State of Florida
TAMPA, FL
This is a professional clinical nursing position for the Medical Foster Care (MFC) program reporting to the Senior Registered Nursing Supervisor position. We are looking for a dedicated…
Added 1 min ago
Student Services Advisor 2 - 142000
UC San Diego/UC San Diego Health
San Diego, CA
Under the supervision of the Associate Director of Student Services, this position provides professional staff support for the administration and implementation of the Graduate educational…
Added 2 mins ago
FM
Travel Cath Lab Technologist
Fusion Medical Staffing
Chillicothe, OH
- $2,744.15 to $3,154.2 USD / week
…while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical…

Actalent

Clinical Research Coordinator

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 the full lifecycle of oncology clinical trials, from protocol initiation and activation through patient enrollment, data collection, safety reporting, and ongoing sponsor communication. This role ensures that all studies adhere to regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines while providing high-quality support to research nurses, physicians, and patients.

Responsibilities

Coordinate the initiation and activation of new clinical trial protocols, ensuring completion and verification of Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance/contract approvals prior to study activation.
Prepare and organize study tools, including study binders, medication diaries, eligibility checklists, calendars, and flow sheets, to support accurate and efficient trial conduct.
Use clinical trials management systems and software such as Excel and Word to develop and maintain study tools, tracking documents, and patient-related materials.
Collaborate with Research Nurse Clinicians and physicians to review patients charts and medical histories, confirm protocol eligibility, and obtain necessary source documents and medical record documentation.
Ensure that IRB-approved informed consent forms are properly obtained, signed, documented in the medical record, and that copies are provided to patients in accordance with regulatory and institutional requirements.
Register consented research patients with study sponsors, including industry partners and National Cancer Institute (NCI) cooperative groups, and enter patient and study data into the clinical trials database.
Maintain complete and accurate research records for all patients enrolled on clinical trials, including patient consent forms, eligibility documentation, case report forms (CRFs), registration confirmations, and corresponding source documents, across centers, community physicians offices, and hospitals.
Assist, in collaboration with the Research Nurse Clinician and physician, in grading adverse events using the most recent NCI common toxicity criteria or protocol-specific grading scales.
Complete Serious/Unexpected Adverse Event (SAE) forms for internal and multicenter serious or unexpected adverse events as required by study sponsors, federal regulations, and institutional guidelines.
Provide regular reports to tumor study group members and Principal Investigators on assigned studies using the clinical trials database and other reporting tools.
Serve as a liaison with study sponsors, understanding and anticipating sponsor needs, scheduling monitoring visits and conference calls, and providing accurate, timely, and well-supported responses to sponsor queries.
Work with Research Nurse Clinicians to ensure that investigators and other personnel conduct studies according to the treatment plan, protocol requirements, and GCP guidelines.
Support screening and recruitment of patients for clinical trials, helping to coordinate study visits and ensure smooth patient flow through the research process.
Communicate comfortably and professionally with patients, answering questions related to study procedures and coordinating their participation in clinical trials.

Essential Skills

Bachelors degree required.
One to three years of relevant clinical research experience, preferably as a Clinical Research Coordinator or in a similar role.
Experience in oncology clinical research, including familiarity with tumor study groups and oncology-specific protocols.
Demonstrated experience with informed consent processes, including obtaining, documenting, and maintaining consent forms in accordance with IRB requirements.
Ability to recruit, screen, and enroll patients into clinical trials while maintaining protocol eligibility standards and accurate source documentation.
Solid knowledge of computer software programs such as Excel, Word, and Access for data tracking, reporting, and development of study tools.
Comfort and experience communicating directly with patients in a clinical research or healthcare setting.
Strong attention to detail and ability to maintain accurate, complete research records and case report forms.
Excellent organizational skills with the ability to manage multiple studies, deadlines, and competing priorities.
Strong written and verbal communication skills and the ability to interact effectively with physicians, nurses, sponsors, and other research staff.
Ability to follow GCP guidelines and institutional policies in the conduct of clinical trials.

Additional Skills & Qualifications

Experience working with oncology disease-specific groups such as breast, lung, gastrointestinal, phase I, or other tumor-focused teams.
Familiarity with NCI common toxicity criteria and protocol-specific grading scales for adverse event assessment.
Experience completing Serious/Unexpected Adverse Event (SAE) documentation for industry-sponsored and cooperative group trials.
Ability to provide clear, timely, and well-organized responses to study sponsors and regulatory monitors.
Demonstrated ability to be detail-oriented, self-accountable, and committed to high standards of professional excellence.
Resourceful mindset with the ability to maximize available resources and proactively solve problems.
Strong interpersonal skills and the ability to build collaborative relationships with multidisciplinary teams, including clinical operations, regulatory affairs, quality assurance, informatics, education, and finance.
Commitment to ongoing personal and professional responsibility and continuous improvement in clinical research practices.

Work EnvironmentThe role operates within a large, dynamic clinical operations structure that includes disease-specific groups such as breast, lung, phase I, and gastrointestinal, as well as dedicated teams in regulatory affairs, quality assurance, informatics, education, and finance. The organization supports approximately 100 full-time research staff and manages around 300 active trials across all phases for both adult and pediatric populations, with roughly 5,000 subjects enrolled per year and a long-term goal of significantly expanding active subject enrollment. Work spans a main site in Newark and multiple affiliated locations across the state, supporting community physicians offices and hospitals. The environment is fast-paced and highly collaborative, with substantial enrollment needs and exposure to a wide range of oncology studies, offering opportunities to work with complex protocols, sophisticated clinical trial management systems, and multidisciplinary teams dedicated to advancing cancer research. Job Type & LocationThis is a Contract to Hire 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 to Hire 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
Clinical trials
Google Cloud
Research
Microsoft Excel
Microsoft Word
Documentation
Scheduling
Perform studies and field investigation
Microsoft Access
Reporting
Attention to detail
Organizational skills
Communication skills
Interpersonal skills
Regulatory affairs
Quality assurance
Process improvement

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