<p>Job Title: Clinical Research Coordinator</p> <p>Job Description</p> <p>The Clinical Research Coordinator will play a pivotal role in coordinating the initiation and activation of new clinical trial protocols, ensuring all necessary study tools are prepared and utilized effectively. This position requires a robust background in data management and clinical research, with a strong focus on oncology trials.</p> <p>Responsibilities</p> <ul> <li>Coordinate the initiation and activation of all new clinical trial protocols. </li><li>Prepare study tools including study binders, medication diaries, eligibility checklists, and flow sheets using Oncore, Excel, and Word. </li><li>Collaborate with the Research Nurse Clinician and/or physician to review patients' charts and medical history to confirm protocol eligibility and obtain necessary source documents. </li><li>Ensure IRB-approved informed consent forms are obtained, signed, and correctly filed in medical records, providing copies to patients. </li><li>Maintain comprehensive research records for all patients enrolled in studies, including consent, eligibility, Case Report Forms, and registration confirmations. </li><li>Assist with grading adverse events and complete Serious/Unexpected Adverse Event forms as required by study sponsors and institutional guidelines. </li><li>Provide regular reports to tumor study group members and Principal Investigators on assigned studies using Oncore. </li><li>Serve as a liaison with study sponsors, scheduling monitoring visits and conference calls, and respond accurately and timely to sponsors' queries. </li></ul> <p>Essential Skills</p> <ul> <li>Minimum of 4 years of clinical research experience. </li><li>At least 4 years of oncology experience. </li><li>Experience working in multiple EDC systems, specifically Medidata and Inform. </li><li>Strong background in data management, with 60% of the role focusing on data coordination. </li><li>Experience in recruiting, screening, and consenting patients for clinical trials. </li><li>Blood processing experience is required. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's Degree is required. </li><li>Experience can come from clinical research, school, or nursing backgrounds, particularly in gynecology oncology groups. </li></ul> <p>Work Environment</p> <p>This position requires onsite work in the Bronx four days a week. The work involves collaboration with tumor study group members, Principal Investigators, and study sponsors, utilizing multiple EDC systems in a clinical setting.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $35.00 - $39.00/hr.</p> <p>Eligibility requirements apply to some benefits and may depend on your job</p> <p>classification and length of employment. Benefits are subject to change and may be</p> <p>subject to specific elections, plan, or program terms. If eligible, the benefits</p> <p>available for this temporary role may include the following:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <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 Jul 11, 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>