<p>Job Title: Clinical Research Coordinator</p> <p>Job Description</p> <p>The Clinical Research Coordinator is responsible for coordinating the initiation and activation of all new clinical trial protocols. This role involves preparing study tools such as study binders, medication diaries, eligibility checklists, and flow sheets. The coordinator will work closely with the Research Nurse Clinician and/or physician to review patients' charts and confirm protocol eligibility.</p> <p>Responsibilities</p> <ul> <li>Coordinate the preparation of study tools, including study binders, medication diaries, eligibility checklists, and flow sheets. </li><li>Develop study tools using Oncore, Excel, and Word, such as eligibility checklists, medication diaries, calendars, and flow sheets. </li><li>Collaborate with the Research Nurse Clinician and/or physician to review patients' charts and medical history to confirm protocol eligibility and obtain source documents. </li><li>Ensure that IRB approved informed consent forms are obtained, signed, placed in the medical record, and provided to the patient. </li><li>Maintain research records for all patients enrolled in studies, including patient consent, eligibility, Case Report Forms, registration confirmation, and corresponding source documents. </li><li>Assist with grading adverse events using the latest National Cancer Institute common toxicity criteria or protocol-specific grading scales. </li><li>Complete Serious/Unexpected Adverse Event forms for all internal and multicenter serious/unexpected adverse events as required. </li><li>Provide regular reports to tumor study group members and the Principal Investigator on all assigned studies using Oncore. </li><li>Serve as a liaison with study sponsors, schedule monitoring visits and conference calls, and provide accurate and timely responses to sponsors' queries. </li></ul> <p>Essential Skills</p> <ul> <li>2+ years of clinical research experience. </li><li>2+ years of oncology experience. </li><li>Experience in data management and coordination, with 60% of the job focused on these tasks. </li><li>Experience working in multiple EDC systems, with preference for Medidata and Inform. </li><li>Experience recruiting, screening, and consenting patients for clinical trials. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's degree in a relevant field. </li><li>Blood processing experience. </li><li>Experience in gynecology oncology groups is acceptable. </li><li>Well-rounded skills in recruiting patients and data collection/data entry. </li></ul> <p>Work Environment</p> <p>The position is based on-site in the Bronx, requiring attendance four times per week. The work primarily involves data management and patient interaction in a clinical setting.</p> <p>Job Type & Location</p> <p>This is a Contract to Hire position based out of bronx, NY.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $30.00 - $35.00/hr.</p> <p>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)</p> <p>Workplace Type</p> <p>This is a hybrid position in bronx,NY.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Dec 26, 2025.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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.</p>