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Summary
About the Role
About You
- Bachelor’s Degree in a scientific discipline or healthcare preferred.
- Minimum 5 years of onsite monitoring experience.
- In-depth knowledge of applicable clinical research regulatory requirements, such as ICH-GCP guidelines.
- Ability to travel up to 80%, including overnight stays.
- Effective organizational, communication, and interpersonal skills.
- Experience managing serious adverse events in collaboration with safety surveillance.
- Experience in clinical trial management systems (CTMS), EDC platforms, and Microsoft Office suite.
- Experience managing aspects of CRO functions.
- Prior experience in patient recruitment & retention strategies and site relationship management.
Benefits
- Tuition reimbursement: 8K per year.
- Holiday Pay: 12 days per year.
- Vacation: at least 10 days annually.
- Sick days: 5.
- Annual performance bonus: 10 – 15%.
- Cell phone reimbursement: $125 per month.
- 5% matching 401K.
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research. Actalent is an operating company of Allegis Group, the global leader in talent solutions.