Job Title: Clinical Research CoordinatorJob Description We are seeking a dedicated Clinical Research Coordinator with over 2 years of experience in clinical research, specifically in supporting drug trials. This role involves patient interaction and meticulous data entry, with a focus on adverse event collection. Responsibilities + Coordinate and oversee clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines. + Conduct chart reviews and manage patient recruitment processes. + Pre-screen patients for clinical trials and manage regulatory documentation. + Enter and manage data using Electronic Data Capture (EDC) systems. + Collaborate with cross-functional teams in oncology to facilitate a variety of trials. Essential Skills + Clinical research and trial management + Experience in chart review and patient recruitment + Knowledge of GCP and regulatory requirements + Proficiency in data entry and EDC systems + Experience in oncology and pre-screening patients Additional Skills & Qualifications + Bachelor's degree in a relevant field with 2+ years of clinical research experience + Experience in a healthcare setting + Successful completion of CITI Program and IATA training within 3 months of hire + Certification in research through a professional organization within 1 year of hire Work Environment The role requires initial training on-site for 4-5 days a week, transitioning to 1 day of remote work per week for the first 6 months. Potential to increase remote work to 3 days per week based on performance and project needs. The work environment fosters growth and offers opportunities to participate in multiple oncology trials, providing a clear path to career advancement. Pay and Benefits The pay range for this position is $25.00 - $30.00/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 hybrid position in Wynnewood,PA. Application Deadline This position is anticipated to close on May 12, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.