<p>Job Title: Clinical Research Coordinator (Oncology)</p> <p>Job Description</p> <p>The Clinical Research Coordinator provides oversight of the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. This role involves functioning as a clinical study coordinator as needed and training, mentoring, and developing clinical study coordinators and research staff within the research enterprise, which may extend across multiple U.S. Division locations.</p> <p>Responsibilities</p> <ul> <li>Supervise day-to-day activities of the clinical research team, including oversight of productivity and maintenance of personnel and staffing schedules. </li><li>Ensure the delivery of safe care with dignity and respect for all patients and participants. </li><li>Serve as a service line expert and resource for the research team when barriers arise during day-to-day operations. </li><li>Monitor and evaluate the quality and safety of clinical operations within the assigned area. </li><li>Build and maintain supportive relationships with team members through regular interactions. </li><li>Collaborate with operations manager, study intake, research services, and external partners to ensure timely start-up and smooth transition to assigned coordinators. </li><li>Develop and maintain Standard Operating Procedures (SOPs) and ensure clinical research operations teams follow processes and procedures. </li><li>Provide guidance, education, specialized training, and mentorship to promote growth for study team members. </li><li>Coordinate effective and compliant clinical research studies, planning, organizing, and managing all activities related to clinical research protocols. </li><li>Support preceptorship of new team members, monitoring progress and communicating with the Operational Manager for workflow planning. </li></ul> <p>Essential Skills</p> <ul> <li>Clinical research expertise </li><li>Oncology knowledge </li><li>Project management skills </li><li>Clinical study coordination </li><li>Clinical trial management </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's Degree in Healthcare Administration, Research, or related field with 2 years of experience in clinical research or </li><li>Associates degree in Healthcare Administration, Research, or related field with 4 years of experience in clinical research or related field </li><li>Basic Life Support (BLS) Certification </li></ul> <p>Pay and Benefits</p> <p>The pay range for this position is $90000.00 - $109000.00/yr.</p> <p>Benefits from Day One</p> <p>Paid Days Off from Day One</p> <p>Student Loan Repayment Program</p> <p>Career Development</p> <p>Whole Person Wellbeing Resources</p> <p>Mental Health Resources and Support</p> <p>Pet Insurance*</p> <p>Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)</p> <p>Nursing Clinical Ladder Program*</p> <p>Workplace Type</p> <p>This is a fully onsite position in Orlando,FL.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Jun 27, 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>