Job Title: Clinical Research Coordinator IIIJob Description Coordinates, implements, and evaluates clinical research trials, studies, and projects. Provides direction in the development of research protocols. Recruits and screens potential study participants and develops and conducts patient and family education accordingly. Oversees financial accounts to ensure operations remain within approved levels. Performs patient evaluations, administers medications and research instruments, and provides nursing support to perform specialized diagnostic, therapeutic, and surgical procedures. Makes referrals to in-house or community professionals and serves as a clinical resource. Collects data, assists in developing data collection systems, and compiles reports. Provides direction and may support other Research Coordinators or other support members. Performs related responsibilities as required. Responsibilities + Independently manage significant and key aspects of Oncology-related trials including one or more small trials or research projects. + Operate as Oncology Research Coordinator in support of specified Oncology disease group(s). + Perform required patient consents. + Train and provide guidance to less experienced staff. + Oversee data management for research projects. + Interface with research participants and resolve issues related to study protocols. + Authorize purchases for supplies and equipment maintenance. + Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Periodically audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. + Monitor IRB submissions and respond to requests and questions. + Interface with study sponsors, monitor and report SAEs; resolve study queries. + Provide leadership in determining, recommending, and implementing improvements to policies/processes. + Assist in developing grant proposals and protocols. + With appropriate credentialing and training, may perform phlebotomy, specimen collection, or diagnostics. + May perform some supervisory duties. + Perform related approved responsibilities as required. Essential Skills + Oncology research coordination + GCP compliance + CRF and ICF management + Patient consenting + Regulatory knowledge + 3+ years of clinical trials and Oncology research experience + Experience managing interventional drug trials + Managing roughly 7-8 active trials and 15 active patients + Clinical research + Project management + CCRC certification Additional Skills & Qualifications + High School Diploma or GED and 3+ years of clinical research experience + Two years of college in a scientific, health-related, or business administration program and three years of clinical research experience Work Environment Office-based in a hospital clinic setting. Monday to Friday, 8 AM to 5 PM work schedule. Pay and Benefits The pay range for this position is $31.00 - $33.00/hr. 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) Workplace Type This is a fully onsite position in Johns Creek,GA. Application Deadline This position is anticipated to close on Feb 25, 2025. About Actalent 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people 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. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.