Clinical Research Coordinator

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a motivated and detail-oriented Clinical Research Coordinator to facilitate the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various oversight committees, preparing study tools, and ensuring compliance with study protocols and guidelines.ResponsibilitiesCoordinate the initiation and activation of clinical trial protocols, ensuring all necessary approvals are in place.Prepare study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.Develop and maintain study tools using software programs like Excel, Word, and Access.Review patients' charts and medical history to confirm protocol eligibility and obtain source documents.Ensure informed consent forms are obtained, signed, documented, and provided to patients.Register consented research patients with study sponsors and input data into the clinical trials database.Maintain research records for all patients enrolled in clinical trials, including consent forms, eligibility documents, and case report forms.Assist with grading adverse events using the latest NCI common toxicity criteria or protocol-specific grading scales.Complete Serious/Unexpected Adverse Event forms as required by study sponsors and guidelines.Provide regular reports to tumor study group members and Principal Investigators.Serve as a liaison with study sponsors, scheduling monitoring visits and responding to queries.Ensure studies are conducted according to the treatment plan and Good Clinical Practice (GCP) guidelines.Essential Skills1-2 years of clinical research coordinator experience.Strong knowledge of clinical research, oncology, and informed consent processes.Proficiency in software programs such as Excel, Word, and Access.Excellent organizational, communication, and interpersonal skills.Additional Skills & QualificationsBachelor's Degree required.Experience in screening patients and coordinating study activities.Comfortable communicating with patients.Detail-oriented and resourceful with a commitment to professional excellence.Job Type & LocationThis is a Contract to Hire position based out of Newark, NJ.Pay and BenefitsThe pay range for this position is $30.00 - $33.00/hr.Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable for this temporary role may include the following:Medical, dental & visionCritical Illness, Accident, and Hospital401(k) Retirement Plan - Pre-tax and Roth post-tax contributions availableLife Insurance (Voluntary Life & AD&D for the employee and dependents)Short and long-term disabilityHealth Spending Account (HSA)Transportation benefitsEmployee Assistance ProgramTime Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Newark,NJ.Application DeadlineThis position is anticipated to close on Dec 3, 2025.About ActalentActalent 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.