Job Title: Clinical Research CoordinatorJob Description We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. The ideal candidate will be responsible for recruiting and screening patients, executing informed consent forms, performing assessments, and managing data entry for clinical studies. This role requires adherence to ICH and GCP guidelines and involves various tasks such as phlebotomy, processing samples, and monitoring investigational products. Responsibilities + Recruit and screen patients for clinical studies. + Execute Informed Consent Forms according to ICH and GCP guidelines. + Perform assessments at study visits according to protocol and document them in source according to ALCOA-CCC. + Perform phlebotomy, process, and ship blood and urine samples according to protocol. + Enter source document data into respective EDC vendor systems (e.g., Medidate RAVE) and respond to queries in a timely manner. + Perform vitals, ECG, and other study assessments required by protocol. + Record adverse events and serious adverse events per sponsor guidance, and maintain timely follow-up to determine resolution of adverse events. + Monitor, dispense, and collect investigational product; maintain accountability logs and temperature logs, and report temperature excursions. + Schedule, prepare, and conduct visits (e.g., SIV, IMVs, COV) with sponsor/CRO team. Essential Skills + Pre-screening patients + Clinical research + Clinical trial management + Patient recruitment + Project management + GCP certification + IATA certification Additional Skills & Qualifications + Understanding of risk variants associated with kidney disease. + Knowledge of how risk variants can affect progression to end-stage renal disease (ESRD). + Familiarity with improving the safety of living kidney donation and the quality of deceased donor kidneys. + Ability to identify people with a higher risk of kidney disease with a poorer prognosis and faster progression. Work Environment The Clinical Research Coordinator will work in a clinical setting, utilizing technologies such as EDC vendor systems and IRT systems. The role involves interaction with patients, sponsors, and CRO teams. The environment requires adherence to strict protocols and guidelines to ensure the safety and accuracy of clinical studies. Pay and Benefits The pay range for this position is $35.00 - $38.00/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 Evergreen Park,IL. Application Deadline This position is anticipated to close on Feb 7, 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.