<p>Join a professional, customer-focused pharmaceutical company as a Clinical Trials Project Coordinator. This role involves supporting the maintenance of study records and coordinating study activities. You will develop, maintain, and archive files and records related to multiple clinical trials while providing administrative support. This position offers a competitive salary and a full benefits package.</p> <p>Responsibilities</p> <ul> <li>Work with the Project Management team to assist in planning investigator meetings. </li><li>Develop required materials, including training tools. </li><li>Initiate contract/budget requests, track status, and negotiate budgets with sites and vendors if necessary. </li><li>Participate in vendor selection and management. </li><li>Identify changes in the scope of work. </li><li>Formulate, track, measure, and maintain a project-specific matrix and timelines. </li><li>Schedule and manage agenda updates and meeting minutes for project team meetings. </li><li>Develop monthly reports, newsletters, and communication trackers. </li><li>Provide administrative support such as mass site communication distribution, shipping, filing, tracking, and summarization. </li><li>Assist in the clinical trial insurance process by tracking approvals, revisions, and renewals of certificates. </li><li>Maintain and track all project-specific invoices. </li><li>Ensure a smooth site start-up process prior to Site Initiation Visits. </li><li>Assist the Clinical Operations team with maintaining the trial master file, study site records, and files. </li><li>Review essential study documents. </li><li>Develop project-specific procedural documents as needed. </li><li>Prepare and ship IRB/EC dossiers. </li><li>Assist the study team with training and access management for CTMS and other trial-related applications. </li><li>Prepare for study-specific audits and inspections. </li><li>Perform other duties as assigned by senior management. </li></ul> <p>Essential Skills</p> <ul> <li>Proficient in Microsoft Office (Word, Excel, PowerPoint). </li><li>Well-organized with strong attention to detail. </li><li>Excellent verbal and written communication skills. </li><li>Fluent in English; other languages are a plus. </li><li>Ability to work independently and with flexibility to accommodate international meeting schedules. </li><li>Strong interpersonal skills. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Minimum of an associate's degree; bachelor's degree preferred. </li><li>Previous experience in a healthcare company. </li><li>Experience with trial master file maintenance, auditing, and reconciliation preferred. </li><li>Experience with archival of paper files and auditing archived files. </li><li>Meeting agenda and minute-taking experience. </li><li>Experience interacting with Contract Research Organizations and third-party vendors. </li><li>Experience with Electronic Trial Master File systems. </li><li>Experience in clinical trial management systems. </li></ul> <p>Pay and Benefits</p> <p>The pay range for this position is $70000.00 - $90000.00/yr.</p> <p>Tuition reimbursement: 8K per year</p> <p>Holiday Pay 12 per year</p> <p>Vacation: at least 10 days annually</p> <p>Sick days 5</p> <p>Annual performance bonus 10 - 15%</p> <p>Cell phone reimbursement $125 per month</p> <p>Workplace Type</p> <p>This is a hybrid position in Pennington,NJ.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Jul 9, 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>