Clinical Research Coordinator: Trials & Enrollment

Actalent; Philadelphia (Philadelphia County); Hybrid; USD 34,000 - 43,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan – Pre-tax and R

Life Insurance (Voluntary Life & AD&D)

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent in Philadelphia, PA is seeking a dedicated Clinical Research Coordinator to support clinical trials by recruiting, screening, and enrolling subjects. The role involves explaining informed consent, documenting adverse events, and collecting essential study and regulatory documents.

You will prepare IRB applications and work in a hybrid office/hospital setting within a leading academic research environment with access to state-of-the-art facilities.

Qualifications

• Proficiency in patient enrollment and consenting.
• Experience in clinical trials and research coordination.
• Familiarity with GCP guidelines.
• Ability to conduct chart reviews and pre-screen patients.
• Experience with data entry using EPIC systems.
• Strong written and verbal communication skills.
• Knowledge of IRB and human research protections.

Responsibilities

• Recruit, screen, and enroll subjects into clinical trials.
• Explain informed consent to participants.
• Document and report adverse events.
• Collect and maintain study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.
• Prepare and submit IRB applications.

Skills

Patient enrollment

Consent process

GCP knowledge

Chart review

Data entry (EPIC)

Communication skills

IRB regulations

Education

BA/BS degree preferred

Tools

EPIC Systems

Job description

Actalent in Philadelphia, PA is seeking a dedicated Clinical Research Coordinator to support clinical trials by recruiting, screening, and enrolling subjects. The role involves explaining informed consent, documenting adverse events, and collecting essential study and regulatory documents.

You will prepare IRB applications and work in a hybrid office/hospital setting within a leading academic research environment with access to state-of-the-art facilities.