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Centralized Clinical Trial Manager

2+ years
Not Disclosed
10 Oct. 17, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Position: Centralized Clinical Trial Manager
Location: Home Based

ICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to fostering an inclusive environment that drives innovation and excellence. We invite you to join us in our mission to shape the future of clinical development.

Job Summary:

The Centralized Clinical Trial Manager (CTM) plays a crucial role in ensuring the quality and efficiency of clinical trial operations. You will be responsible for reviewing visit reports, liaising between team members, and ensuring that clinical trial processes meet the highest standards.

Key Responsibilities:

  • Effectively review and approve visit reports according to protocols and ICON/Sponsor SOPs, minimizing errors and maintaining quality.
  • Follow up on action items and protocol deviations, acting as a liaison between CRAs, CTMs, and PMs for timely issue resolution.
  • Escalate safety trends identified in visit reports to appropriate stakeholders.
  • Regularly oversee key metrics in OMR, ICOtrial, and Sponsor systems to ensure compliance with timelines and quality standards.
  • Attend project meetings to provide suggestions for improving report quality and addressing outstanding issues.
  • Communicate any trends, safety concerns, or activities that may jeopardize trial delivery or patient safety.
  • Complete necessary training to enhance job performance and knowledge.
  • Contribute to quality improvement and risk management plans.
  • Support change management initiatives and collaborate with other managers to enhance organizational effectiveness.

Benefits of Working at ICON:

We believe that our success depends on the quality of our people, which is why we prioritize building a culture that rewards high performance and nurtures talent. Our benefits include:

  • Competitive salary packages, regularly benchmarked against industry standards.
  • Annual bonuses based on performance goals.
  • Comprehensive health benefits for you and your family.
  • Competitive retirement plans with life assurance.
  • Flexible benefits such as childcare vouchers, gym memberships, and more.

Commitment to Diversity and Inclusion:

ICON is an equal opportunity and inclusive employer, committed to providing a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If you require reasonable accommodation during the application process, please let us know.

Interested in the Role?

If you’re passionate about advancing clinical research and improving patient lives, we encourage you to apply, even if you don’t meet every requirement. You may be exactly what we’re looking for!