Job Description
We are seeking a dedicated Clinical Research Coordinator to join our team. The ideal candidate will be responsible for recruiting, screening, and enrolling subjects into clinical trials. You will also play a key role in explaining the informed consent process, documenting adverse events, and collecting various study documents and protocols. Additionally, you will prepare Institutional Review Board (IRB) applications.
ResponsibilitiesRecruit, screen, and enroll subjects into clinical trialsExplain the informed consent process to study participantsDocument adverse events in a timely and accurate mannerCollect study documents, protocols, regulatory documents, informed consents, case report forms, and source documentsPrepare and submit Institutional Review Board (IRB) applicationsEssential SkillsExperience with patient recruitment and consentingStrong understanding of the informed consent processProficiency in documenting adverse eventsKnowledge of IRB and human research protection regulations2+ years of clinical research experienceEffective communication and writing skillsAdditional Skills & QualificationsBachelor's degree (BA/BS) preferredExperience with in-hospital clinical researchFamiliarity with oncology clinical trialsKnowledge of Good Clinical Practice (GCP) and Electronic Data Capture (EDC)Work Environment
This position involves working in a combination of office and hospital/outpatient surgery settings. The work environment is very fast-paced with a high volume of industry and investigator studies. You will be part of one of the most prestigious academic research institutes in the world, working with state-of-the-art equipment on high-profile studies sponsored by well-known organizations.
Pay and BenefitsThe pay range for this position is $28.00 - $31.25/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 May 19, 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 for other accommodation options.