About the Company
ICON plc is a world-leading provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. We specialize in the strategic development, management, and analysis of programs that support the clinical development of new products. With a global presence, we are committed to improving patients’ lives by accelerating the development of new drugs and devices.
Job Description
We are seeking a highly motivated and experienced Clinical Trial Manager to join our growing team in Fredericton. This pivotal role involves the comprehensive oversight and management of clinical trials from start-up through close-out, ensuring adherence to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements. The successful candidate will be responsible for leading study teams, managing budgets and timelines, and serving as the primary point of contact for sponsors and investigative sites. A generous relocation package is available for qualified candidates.
Key Responsibilities
- Lead the planning, execution, and close-out of assigned clinical trials within agreed timelines and budgets.
- Manage all aspects of study start-up, including protocol development, site selection, and regulatory submissions.
- Oversee clinical monitoring activities, ensuring data integrity and patient safety.
- Develop and maintain strong relationships with investigative sites, vendors, and sponsors.
- Monitor study progress, identify potential risks, and implement mitigation strategies.
- Ensure compliance with all applicable regulations, GCP, and company SOPs.
- Manage study budgets, track expenditures, and provide financial reports.
- Mentor and provide guidance to junior clinical trial staff.
Required Skills
- Minimum of 5 years of experience in clinical research, with at least 2 years in a clinical trial management role.
- Demonstrated knowledge of Good Clinical Practice (GCP) and relevant regulatory requirements.
- Strong project management skills, including the ability to manage multiple projects simultaneously.
- Excellent communication, leadership, and interpersonal skills.
- Proficiency in clinical trial management systems and Microsoft Office Suite.
- Bachelor's degree in a life science or related field.
Preferred Qualifications
- Master's degree in a relevant scientific or health-related discipline.
- PMP certification or equivalent project management qualification.
- Experience with global clinical trials.
- Familiarity with various therapeutic areas, particularly oncology, cardiovascular, or CNS.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and holidays.
- Retirement savings plan with company match.
- Professional development and continuing education opportunities.
- Relocation assistance package available.
- Collaborative and supportive work environment.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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