Freelance Clinical Research Associate
TFS, Luxembourg
Job Description
The Senior Clinical Research Associate (Sr CRA) is part of SRS and COP within TFS Develop and will function operationally as a member of a Project Team and is responsible for the initiation, on-site and remote monitoring and termination of investigative sites during study conduct, according to company policies, SOPs and regulatory requirements. The Sr CRA may assist the Project Manager in certain aspects of project activities which may include project tracking, monitoring plans, review of monitoring reports and CRA resources management. The Sr CRA may also conduct all stages of site monitoring (feasibility, pre-study, initiation, interim, and close-out). Ability to travel as needed; may involve overnight and international travel.
Requirements
- Bachelor’s Degree, preferably in life science or nursing; or equivalent
- 3-5 years of experience as CRA including relevant on-site monitoring experience
- Able to work in a fast paced environment with changing priorities
- Understand the basic medical terminology and science associated with the assigned drugs and therapeutic areas
- Possess the understanding of Good Clinical Practice regulations, ICH guidelines
- Ability to work independently as well as in a team matrix organization
- Excellent written and verbal communication skills
- Excellent organizational skills
- Ability and willingness to travel up to 60-70%
Benefits
- Work From Home
- Training amp; Development