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Pediatric Nurse - Clinical Trial Sites In County Clare, Ireland

0-2 years
Not Disclosed
10 Jan. 3, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Research Assistant
Company: ProPharma Group
Location: Remote
Position Type: Full-Time


About ProPharma Group

For the past 20 years, ProPharma has been committed to improving patient health by empowering biotech, pharmaceutical, and medical device organizations to successfully advance scientific breakthroughs and deliver new therapies. As the world’s largest Research Consulting Organization (RCO), ProPharma offers a complete suite of customizable solutions across the entire product lifecycle. With deep expertise in regulatory sciences, clinical research, pharmacovigilance, quality & compliance, and more, ProPharma accelerates the success of high-profile drug and device programs.


Position Overview

ProPharma is looking for a Clinical Research Assistant to support clinical monitoring for assigned protocols and investigational sites. This position ensures studies are conducted in compliance with study protocols, Good Clinical Practices (GCP), and regulatory requirements. The Clinical Research Assistant will collaborate with team members to ensure the quality and integrity of the clinical trial process.


Key Responsibilities

  • Clinical Monitoring & Documentation:

    • Ensure studies are executed according to protocol, GCP, and regulatory standards.
    • Assist with study documentation and monitoring of investigational sites.
  • Collaboration:

    • Work closely with Research Associates (RAs) and Clinical Study Coordinators (CSCs) to complete tasks effectively.
  • Technology Management:

    • Utilize web-based research platforms and PC tools for remote work and study management.
  • Communication & Problem-Solving:

    • Communicate progress, issues, and resolutions with the study team.
    • Apply critical thinking skills to address challenges and assist in study execution.

Minimum Qualifications

  • Research Experience: Previous experience in research is preferred.
  • Technology Skills: Proficiency in managing web-based research platforms on Microsoft OS.
  • Study Team Experience: Prior experience as part of a study team is ideal.
  • Communication Skills: Strong verbal and written communication abilities.
  • Critical Thinking: Excellent problem-solving and analytical skills.
  • Independent & Team Collaboration: Ability to work independently and with others to complete tasks.
  • Privacy: Ability to maintain privacy in a remote work environment.

Additional Information:

  • ProPharma embraces diversity, equity, and inclusion in the workplace, encouraging employees to bring their authentic selves and contributing to a culture of success.
  • #LI-Remote
  • Note: ProPharma does not accept unsolicited resumes from recruiters or third parties.

How to Apply:

Interested candidates should apply directly through ProPharma’s career portal.


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