Clinical Research Coordinator

Actalent; Philadelphia (Philadelphia County); Hybrid; Full time

Job summary

A leading company is seeking a Clinical Research Coordinator to manage clinical trials, recruit participants, and ensure compliance with regulatory standards. This role offers a dynamic work environment combining office and hospital settings with opportunities for professional growth.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account

Transportation benefits

Employee Assistance Program

Time Off/Leave

Qualifications

• At least 2 years of experience in clinical research.
• Experience with in-hospital clinical research settings.

Responsibilities

• Manage and coordinate clinical trials.
• Recruit, screen, and enroll subjects into clinical trials.
• Document adverse events during the trials.

Skills

Enrollment

Informed Consent

Patient Management

Clinical Research Coordination

Good Clinical Practice

Electronic Data Capture

Chart Review

Effective Communication

Education

Bachelor's Degree

Job description

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Job Title: Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator who will play a vital role in managing and coordinating clinical trials. The position involves recruiting, screening, and enrolling subjects into clinical trials, explaining the informed consent process, and documenting adverse events. You will also be responsible for collecting study documents, protocols, regulatory documents, informed consents, case report forms, and source documents, as well as preparing Institutional Review Board (IRB) applications.

Responsibilities

• Recruit, screen, and enroll subjects into clinical trials.
• Explain the informed consent process to participants.
• Document adverse events during the trials.
• Collect study documents, protocols, regulatory documents, informed consents, case report forms, and source documents.
• Prepare IRB applications for trial approval.
  
  

Essential Skills

• Experience with enrollment and informed consent processes.
• Knowledge of patient management in oncology trials.
• Proficiency in clinical research coordination and trial management.
• Understanding of Good Clinical Practice (GCP) and Electronic Data Capture (EDC).
• Experience in chart review and patient consenting.
  
  

Additional Skills & Qualifications

• Bachelor's degree in a related field is preferred.
• At least 2 years of experience in clinical research.
• Experience with in-hospital clinical research settings.
• Proficiency in adverse event reporting.
• Experience in patient recruitment and consenting.
• Effective communication and writing skills.
• Knowledge of IRB and human research protection regulations.
  
  

Work Environment

This role operates within a combination of office and hospital/outpatient surgery settings. The work environment is fast-paced and involves a high volume workload of industry and investigator studies. You will have the opportunity to work at one of the most prestigious academic research institutes in the world, with access to state-of-the-art equipment and high-profile studies sponsored by well-known entities.

Pay and Benefits

The 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 26, 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 [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Business Consulting and Services

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