(Senior) Clinical Trial Manager (II), IQVIA Biotech
About The Position
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. This role offers the opportunity to lead complex, global clinical trials and help bring innovative therapies to patients faster. You will join a high-performing team where you'll drive clinical strategy, lead international study teams, and play a critical role in delivering world-class research programs. As a Senior Clinical Lead, you will provide leadership and oversight for large, multi-regional clinical trials, ensuring studies are delivered on time, within scope, and to the highest quality standards. You'll partner with cross-functional teams, sponsors, and stakeholders to navigate challenges, drive recruitment success, manage risk, and achieve key project milestones.
Requirements
- Bachelor's degree in a scientific, healthcare, or related field.
- Sr CTM Requirements: 7+ years of clinical research experience, including monitoring and clinical trial leadership.
- CTM II Requirements: 5+ years of clinical research experienced, including monitoring and clinical trial leadership.
- Strong knowledge of clinical operations, ICH-GCP guidelines, and global regulatory requirements.
- Experience leading complex, multi-country studies and cross-functional teams.
- Understanding of project management principles and clinical trial financial oversight.
- Excellent communication, stakeholder management, and problem-solving skills.
- Proven ability to influence, mentor, and drive results in a fast-paced environment.
Responsibilities
- Lead the clinical delivery of large global clinical trials from startup through closeout.
- Drive patient recruitment and retention strategies to meet enrollment goals.
- Identify, assess, and mitigate clinical and operational risks.
- Oversee clinical quality, ensuring compliance with ICH-GCP, regulatory requirements, and study protocols.
- Partner with project leadership to manage timelines, budgets, and resource planning.
- Build, mentor, and guide clinical teams to deliver exceptional results.
- Collaborate with internal and external stakeholders across multiple regions and cultures.
- Support proposal development, bid defenses, and strategic planning activities.
Benefits
- Incentive plans
- Bonuses
- Other forms of compensation
- Range of health and welfare benefits
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What This Job Offers
Job Type
Full-time
Career Level
Senior
