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Job Title: Clinical Research CoordinatorJob Description

We are seeking a dedicated Clinical Research Coordinator to join our prestigious academic research institute. This role involves recruiting, screening, and enrolling subjects into clinical trials, explaining the informed consent process, documenting adverse events, and collecting essential study documents. The coordinator will also be responsible for preparing Institutional Review Board applications, supporting CAR-T sponsor drug trials, and being part of starting up new studies.

Responsibilities

+ Recruit, screen, and enroll subjects into clinical trials.

+ Explain the informed consent process to participants.

+ Document adverse events as they occur during trials.

+ Collect study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.

+ Prepare Institutional Review Board (IRB) applications.

Essential Skills

+ Enrollment and informed consent process knowledge.

+ Experience in patient oncology research.

+ Proficiency in clinical research coordination and data entry.

+ Ability to conduct chart reviews and understand regulatory requirements.

+ Experience in patient recruitment and consenting.

+ Effective communication and writing skills.

+ Knowledge of IRB and human research protection regulations.

Additional Skills & Qualifications

+ Bachelor's degree (BA/BS) preferred.

+ 1-3 years of clinical research experience required.

+ Experience with in-hospital clinical research.

+ Experience with adverse event reporting.

Work Environment

The role involves working in a combination of office and hospital/outpatient surgery settings, within a very fast-paced and high-volume workload environment. You will be part of the largest team at the cancer center, with ample support, working on high-profile studies with large, well-known sponsors. The institute is equipped with state-of-the-art facilities, and the position offers the opportunity to work on industry-leading and investigator studies.

Pay and Benefits

The pay range for this position is $28.00 - $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 Philadelphia,PA.

Application Deadline

This position is anticipated to close on Jun 13, 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 [email protected] (%[email protected]) for other accommodation options.