Clinical Research Coordinator

Clinical Research Coordinator

Location: Onsite Monday-Friday About the Role We are seeking a Clinical Research Coordinator to oversee and coordinate clinical trial operations across multiple studies. Working closely with the Principal Investigator (PI), this role is responsible for study management, patient enrollment, regulatory compliance, and ensuring high-quality clinical research execution. Key Responsibilities

- Serve as a liaison between investigators, sponsors, research nurses, and regulatory teams.
- Coordinate and oversee daily clinical trial operations.
- Screen, enroll, and consent study participants according to protocol requirements.
- Schedule patient visits, laboratory testing, imaging, and study procedures.
- Monitor study activities to ensure compliance with protocols and regulatory requirements.
- Maintain accurate study documentation, source records, and clinical trial management systems.
- Coordinate sponsor monitoring visits and support audit readiness activities.
- Manage specimen collection, processing, storage, and shipment.
- Support study start-up activities, including protocol review, study calendars, and operational workflows.
- Communicate with participants and healthcare providers to obtain follow-up information.
- Assist with preparation of regulatory documents, reports, presentations, and study-related materials.

Required Qualifications

- Bachelor's degree in Science, Healthcare, or a related field.
- Minimum of 4 years of clinical research experience OR 2+ years in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role.
- Strong understanding of clinical research regulations and study conduct.
- Experience supporting Principal Investigators and clinical study teams.
- Excellent organizational, communication, and documentation skills.
- Ability to manage multiple studies and deadlines in a fast-paced environment.
- Proficiency in Microsoft Office and/or Google Workspace.
- Experience with oncology, specialty, or investigator-initiated research studies.
- Experience with IRB submissions, sponsor interactions, and site monitoring visits.
- Strong patient-facing clinical research experience.
Job Type & Location
This is a Contract to Hire position based out of Paramus, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $40.00/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)
Workplace Type
This is a fully onsite position in Paramus,NJ.
Application Deadline
This position is anticipated to close on Oct 1, 2026. 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 [email protected] 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.