Senior Clinical Trials Project Leader

Pixel Wiser

Dublin

On-site

EUR 70,000 - 95,000

Full time

3 days ago
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Job summary

Pixel Wiser in Ireland is seeking a seasoned project manager to oversee IRC projects within the clinical trial sector. You will develop project plans, monitor progress, and ensure compliance with GCP and company SOPs.

The role requires a bachelor’s degree and a GCP certificate, with 5+ years in clinical trials or 2+ in IRC, plus strong communication, planning, and risk management skills. You will collaborate across teams and guide project teams through challenges.

Qualifications

  • Bachelor’s degree or above in clinical medicine, pharmacy, medical sciences, management, or related fields.
  • GCP certification and familiarity with trial regulations; basic medical imaging knowledge.
  • 5+ years in clinical trials or 2+ in IRC industry.
  • Ability to work under pressure with strong communication and meticulous attention to detail.
  • Strong planning, organization, problem-solving, and risk prevention skills.

Responsibilities

  • Develop PM plans and review documents per GCP, SOPs, and trial protocols.
  • Lead IRC projects, manage budgets/revenue, chair meetings, ensure SOP compliance, address issues.
  • Develop and update departmental policies and internal docs.
  • Provide training, review plans, monitor priorities, predict risks, implement countermeasures.
  • Prepare commercial documents, bids, quotations, and contract reviews.

Skills

GCP certificate
Clinical trial knowledge
Communication skills
Planning & organizing
Risk management
Adaptability
Customer orientation

Education

Bachelor's degree or higher in clinical medicine, pharmacy, medical sciences, management, or related fields

Job description

Pixel Wiser in Ireland is seeking a seasoned project manager to oversee IRC projects within the clinical trial sector. You will develop project plans, monitor progress, and ensure compliance with GCP and company SOPs.

The role requires a bachelor’s degree and a GCP certificate, with 5+ years in clinical trials or 2+ in IRC, plus strong communication, planning, and risk management skills. You will collaborate across teams and guide project teams through challenges.

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