Clinical Research Associate II
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Job Description
Clinical Research Associate II overseeing monitoring visit activities for clinical studies. Working with investigational sites to ensure qualifications and resources are adequate throughout the trials.
Responsibilities:
- Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities
- Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff
- Trains investigational site staff as necessary
- Supports preparation of regulatory and / or EC submissions
- Participates in mentoring/training of new staff as well as performing co-monitoring visits
Requirements:
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials
- Full working proficiency in English
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Benefits:
- Training and career development opportunities internally
- Strong emphasis on personal and professional growth
- Friendly, supportive working environment
- Opportunity to work with colleagues based all over the world, with English as the company language
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