FAQs
What is the work schedule for the Clinical Site Liaison position?
The work schedule is standard, Monday through Friday.
What kind of environment will I be working in?
You will be working in an office environment.
What is the main purpose of the Clinical Site Liaison role?
The main purpose is to support the conduct and patient recruitment of global clinical trials at investigative sites through local and relational support.
What qualifications are required for this position?
A Bachelor's degree in a scientific or health-related field is required, along with a minimum of 6 years of experience in biotech/pharma, preferably in site engagement and/or clinical trial monitoring experience.
Is previous experience in neurology required?
Yes, prior experience in neurology, autoimmune, and rare disease backgrounds is preferred.
Will I need to travel for this role?
Yes, national travel is required, and occasional international travel may also be necessary.
What are the key responsibilities of the Clinical Site Liaison?
Key responsibilities include engaging with clinical sites, supporting patient recruitment, participating in feasibility activities, and collaborating with various teams, including Medical Affairs and Global Patient Advocacy.
What skills are important for success in this role?
Important skills include knowledge of ICH-GCP, strong communication and presentation skills, relationship management abilities, leadership qualities, organizational skills, and problem-solving capabilities.
What type of clinical trials will I be involved with?
You will be involved with global clinical trials, specifically within the neurology franchise and rare disease areas.
Does this position involve oversight activities?
Yes, the role may involve monitoring oversight activities, including accompanying the CRO CRA during site visits to ensure quality conduct of clinical trials.