Study Start Up Manager
hace 7 días
As a Study Start Up Manager at ICON, you will play a critical role in leading a global team of Study Start Up Associates. Your primary responsibility will be to coordinate and facilitate the activities related to preparation, review, and approval of Study Master, country-related, and site-level Informed Consent documents in accordance with internal and external SOPs, such as ICH, GCP, and all applicable regulations, laws, and other guidelines and ethical standards.
Key Responsibilities:
- Lead and drive the creation, review, and approval of Informed Consent Forms and related documentation.
- Build and negotiate processes with Sponsors and Portfolio Directors.
- Deliver training to members of the team and global study teams to ensure quality and alignment of processes.
- Continually assess opportunities for process improvements and develop and monitor process change implementation.
- Provide financial oversight to ensure appropriate profitability and monitor and manage staff workload to optimize resource utilization.
About You
We are looking for a highly experienced and skilled individual with a degree in Life Sciences and a minimum of 5+ years of proven clinical research industry experience. You should have excellent English language skills and be able to work effectively in a dynamic and supportive environment.
Benefits of Working at ICON
- We offer very competitive salary packages and regularly benchmark them against our competitors.
- Our annual bonuses reflect delivery of performance goals - both ours and yours.
- We provide a range of health-related benefits to employees and their families and offer competitive retirement plans.
- We are an equal opportunity and inclusive employer and are committed to providing a workplace free of discrimination and harassment.
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