<p>Job Title: Clinical Research CoordinatorJob Description</p> <p>A Clinical Research Coordinator plays a crucial role in clinical research projects, overseeing and managing various aspects of clinical trials and studies. The primary responsibility is to ensure that research protocols are implemented efficiently, ethically, and in compliance with regulatory requirements.</p> <p>Responsibilities</p> <ul> <li>Coordinate participant study visits and prepare charts and supplies for study visits. </li><li>Lead participant tests, procedures, and eDiary setup. </li><li>Enter data for study visits and maintain participant charts. </li><li>Send participant reminders for eDiary completion, fasting visits, etc. </li><li>Attend site initiation visits (SIV) and interim monitoring visits (IM) for primary studies. </li><li>Interact with study monitors for site-specific and/or patient issues. </li><li>Assist study monitors during scheduled interim monitoring visits (IMV) and close-out visits (COV). </li><li>Engage in remote monitor interactions when necessary. </li><li>Manage investigational product supplies for primary studies and dispense study medication to participants. </li><li>Answer queries for primary studies as needed. </li><li>Complete necessary trainings and keep Investigator Site File (ISF) logs updated for primary studies. </li><li>Act as a point of contact for patient-related escalations/issues such as adverse events (AE), serious adverse events (SAE), compliance issues, eligibility concerns, and unblinding. </li><li>Review medical records with investigators to ensure all study criteria are met. </li><li>Attend and contribute to weekly Clinical Research Coordinator (CRC) meetings and quarterly staff meetings. </li><li>Perform additional duties and projects as assigned. </li></ul> <p>Essential Skills</p> <ul> <li>Experience in pre-screening patients. </li><li>Proficiency in clinical research and familiarity with the role of a Clinical Research Coordinator. </li><li>A degree or equivalent clinical research experience is preferred. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Strong organizational and multitasking skills. </li><li>Excellent communication and interpersonal abilities. </li><li>Proficient in data entry and maintaining accurate records. </li></ul> <p>Work Environment</p> <p>The position is based at a clinical research site that screens and enrolls patients. The site has a team of approximately 15 people, fostering a collaborative and supportive environment.</p> <p>Job Type & Location</p> <p>This is a Contract position based out of Media, PA.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $25.00 - $26.00/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 fully onsite position in Media,PA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Mar 13, 2026.</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>