Clinical Trial Manager

🔥 2 hours ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs. • Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. • Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation. • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight. • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance. • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines. • Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary. • Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

🎯 Requirements

• A minimum of 2+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization. • Bachelor's degree in health, life sciences, or other relevant fields of study. • Preferred: previous monitoring experience • Experience in managing complex or global trials is advantageous. • Preferred: Experience in managing all trial components from start-up to database lock. • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives. • Willingness to travel as required (approximately 25%)

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways