Clinical Trials Lead (Hybrid) - Queenstown

Placements24

O Mente

Hybrid

EUR 48,000 - 70,000

Full time

2 days ago
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Benefits offered by this job

Health benefits
Retirement fund contributions
Hybrid work model
Career development opportunities

Job summary

Placements24 is helping a leading pharmaceutical research organization fill the role of Clinical Project Manager to oversee pivotal multi-site trials from Queenstown, Eastern Cape hub. You will ensure adherence to GCP, ICH, and regulatory standards while coordinating study teams, sites, and vendors.

The ideal candidate has 5+ years in clinical research, strong leadership and budgeting skills, and proficiency with CTMS/EDC.

Qualifications

  • Requires a life sciences degree with relevant clinical research knowledge.
  • 5+ years in clinical research; at least 3 years in project management.
  • Strong knowledge of GCP/ICH and regulatory requirements.

Responsibilities

  • Lead and oversee planning, execution, and monitoring of clinical trials per GCP/ICH.
  • Select, train, and oversee clinical sites and investigators.
  • Develop and manage study budgets and financial reporting.
  • Create and manage project timelines and milestones.
  • Ensure data integrity and quality of trial data.
  • Manage relationships with CROs and central labs.
  • Oversee recruitment and retention of participants.
  • Prepare progress reports for stakeholders and regulators.
  • Identify risks and mitigate issues impacting timelines.
  • Ensure ethical and regulatory compliance throughout the trial lifecycle.

Skills

Leadership
Communication
Interpersonal skills
CTMS experience
EDC systems
Organizational skills
Problem-solving
Multi-project management
English fluency

Education

Bachelor's degree in life sciences
Advanced degree (Masters/PhD)

Tools

CTMS
EDC

Job description

Placements24 is helping a leading pharmaceutical research organization fill the role of Clinical Project Manager to oversee pivotal multi-site trials from Queenstown, Eastern Cape hub. You will ensure adherence to GCP, ICH, and regulatory standards while coordinating study teams, sites, and vendors.

The ideal candidate has 5+ years in clinical research, strong leadership and budgeting skills, and proficiency with CTMS/EDC.

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