Sr. Clinical Research Coordinator

Job Title: Clinical Trial Specialist

Job Description

The Clinical Trial Specialist is responsible for coordinating the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various boards, preparing study tools, and ensuring informed consent forms are properly managed. The specialist will collaborate with research nurses and physicians to confirm protocol eligibility and manage patient records.

Responsibilities

• Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and data collection plans are in place.
• Prepare study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.
• Develop study tools using computer software such as Excel and Word.
• Collaborate with Research Nurse Clinicians and physicians to review patient charts and medical history for protocol eligibility.
• Ensure that informed consent forms are obtained, signed, and properly documented in medical records.
• Register consented research patients with study sponsors and maintain records in the clinical trials database.
• Maintain comprehensive research records for all patients enrolled in clinical trials.
• Assist with grading adverse events and complete necessary forms for serious/unexpected adverse events.
• Provide regular reports to tumor study groups and Principal Investigators on assigned studies.
• Serve as a liaison with study sponsors, schedule monitoring visits, and respond to sponsors queries.
• Ensure that personnel, including investigators, conduct studies according to treatment plans and Good Clinical Practice (GCP) guidelines.

Essential Skills

• 2-3 years of experience as a Clinical Research Coordinator.
• Experience in clinical research, particularly in oncology.
• Proficiency in managing informed consent and source documents.
• Ability to recruit and enroll patients.
• Comfortable communicating with patients.

Additional Skills & Qualifications

• Bachelors Degree required.
• Solid knowledge of computer software programs such as Excel, Word, and Access.
• Detail-oriented with excellent organizational, communication, and interpersonal skills.
• Ability to hold oneself accountable to high standards of professional excellence.
• Resourceful and able to maximize resources effectively.

Work Environment

The role is based at an NCI Designated Cancer Center with a diverse and dynamic team of 100 full-time employees. The team operates across various disease-specific groups including breast, lung, GI, and more. The center enrolls approximately 5,000 subjects annually across Newark and seven other sites. With over 300 active trials, the environment is fast-paced and focused on both adult and pediatric phases.

Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for next steps information.

This is a Contract to Hire position based out of Newark, NJ.

The pay range for this position is $35.00 - $38.00/hr.

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)

This is a hybrid position in Newark,NJ.

This position is anticipated to close on Jun 5, 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 30,000 consultants and more than 4,500 clients across the U.S.,

Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 ... 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.