FSP_Clinical Research Associate (Sponsor: Biogen) ─ with Sign-on Bonus

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

FSP_Clinical Research Associate (Sponsor: Biogen) ─ with Sign-on Bonus

This individual ensures that clinical studies are conducted at investigator sites in compliance with:

the current approved protocol and any protocol amendment(s),

ICH GCP

PPD Written Standards

applicable local laws and regulatory requirement(s)

so that the rights, safety and well-being of human subjects is protected and that the reported study data is accurate, complete, and verifiable from source documents.

• Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, exciting projects.
• Have excellent communication and social skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
• Perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.
• Benefit from award winning training programmes that will assist your technical and professional skills and knowledge.
• Keys to Success:
• Education - University degree in a nursing / life-sciences field
• Experience - Experience of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation ( at least for 3 years )
• Knowledge, Skills, Abilities- Demonstrated understanding of ICH-GCP, MFDS and FDA requirements
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Exceptional communication, collaboration, organizational and time management skill
• Fluency in English languages