Permanent Clinical Trial Manager | IQVIA Vacancies
Job Description
IQVIA Vacancies – Clinical Trial Manager – IQVIA Biotech
Location: Centurion, Gauteng
Company: IQVIA
Job Type: Permanent
Job Sector: Healthcare/Pharmaceuticals
Clinical Trial Manager – IQVIA Biotech
Job Overview
Clinical Trial Managers play a vital role in clinical trial delivery, leading teams to advance patient care by accelerating the development of new therapies. The Clinical Lead is a core member of project teams, responsible for the clinical execution of large, multi-regional studies in compliance with SOPs, regulatory standards, and client agreements. Oncology experience is required.
Essential Functions
- Ensure clinical trial delivery adheres to regulatory requirements (ICH-GCP, protocol), client contracts, and internal policies.
- Achieve recruitment targets by developing and implementing effective enrollment strategies.
- Contribute to risk mitigation plans and manage clinical risks throughout the project lifecycle.
- Oversee clinical quality by defining standards, monitoring compliance, and addressing quality issues.
- Manage project finances, including Estimate at Completion (EAC), and identify opportunities for additional services or scope adjustments.
- Serve as a primary Clinical Lead for large global trials, collaborating with cross-functional teams.
- Engage with internal and external stakeholders, ensuring clear communication and issue resolution.
- Support study milestones and provide regular progress reports to stakeholders.
- Oversee clinical team resourcing, training, and performance to ensure project success.
- Conduct team meetings and provide constructive feedback to support professional development.
- Advocate for corporate initiatives and drive change when necessary.
- Contribute to clinical strategy in business proposals and participate in bid defenses.
- Mentor junior team members and participate in site visits as needed.
Qualifications
- Education: Bachelor’s degree in healthcare, life sciences, or a related field.
Experience
- Minimum of 2 years in clinical trial management or equivalent experience.
- Strong understanding of project management principles and clinical research regulations (ICH-GCP).
- Expertise in protocol execution and therapeutic areas.
- Knowledge of clinical trial operations, industry trends, and financial management.
- Proficiency in clinical research compliance, including local and international guidelines.
Skills
- Communication: Excellent written and verbal English skills.
- Problem-solving: Analytical mindset with strong resolution capabilities.
- Organization: Ability to prioritize tasks and manage time effectively.
- Quality: Detail-oriented with a results-driven approach.
- Leadership: Strong negotiation, decision-making, and mentoring skills.
- Technical: Proficient in Microsoft Office (Word, Excel, PowerPoint).
- Collaboration: Effective team player with cross-cultural awareness.
About IQVIA
IQVIA is a global leader in clinical research, commercial analytics, and healthcare intelligence. We harness data and expertise to accelerate medical innovation and improve patient outcomes worldwide. Learn more at IQVIA.com.
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How to Apply
To apply for this position, click the “Apply Now” button or follow the specific instructions provided in the job description. Ensure that your CV and supporting documents are up to date and relevant to the position.
Please note: This job posting may be closed at any time by the employer, either due to internal recruitment policies, legal requirements, or once a suitable candidate has been found. We encourage you to apply as early as possible.
Only shortlisted candidates will be contacted.
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