Job Description

Clinical Research CoordinatorJob Description Join an exciting opportunity to support cutting-edge oncology studies backed by pharmaceutical leaders. This role involves coordinating clinical trials, managing patient recruitment, and ensuring regulatory compliance in a fast-paced environment. Responsibilities Recruit, screen, and enroll subjects into clinical trials. Explain the informed consent process to participants. Document adverse events and report them appropriately. Collect and manage study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents. Prepare applications for the Institutional Review Board (IRB). Essential Skills Proficiency in enrollment, informed consent, patient recruitment, and consenting. Experience in clinical research coordination, particularly in oncology. Knowledge of Good Clinical Practice (GCP) standards. Ability to conduct chart reviews and pre-screen patients. Strong communication and writing skills. Understanding of IRB and human research protection regulations. Additional Skills & Qualifications Bachelor's degree (BA/BS) preferred. A minimum of 2 years of clinical research experience required. Experience with in-hospital clinical research. Effective communication and writing skills. Work Environment Work in a dynamic combination of office and hospital/outpatient surgery settings. The role is fast-paced with a high volume of industry and investigator studies. After three months, the position offers a hybrid model of three days on-site and two remote. Benefit from state-of-the-art equipment and work on high-profile studies with renowned sponsors. Pay and Benefits The pay range for this position is $28.00 - $32.00/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 Philadelphia,PA. Application Deadline This position is anticipated to close on Aug 15, 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. Actalent

Job Tags

Similar Jobs