CRA II / SCRA required in France

CRA / SCRA’s needed France (Paris) for small CRO

At Upsilon Global we are excited to be working with a small CRO who are looking to expand their Clinical Operations team in France!

This company are looking for ambitious CRA’s on a permanent basis. They are a global provider of complex drug development solutions, across a variety of therapeutic areas. With offices across North America, Europe, and the Middle East, this CRO has experience focusing on some of the most complex development areas including oncology, rare and orphan indications, and cell and gene therapies.

This company boasts a high-performance culture, as they put emphasis on personal development and training. If you’re looking for career progression, a competitive salary, and new skills, then look no further!

Requirements

• Bachelor’s degree in health care or life science related field 1-year independent monitoring experience essential
• Strong knowledge of ICH GCP Guidelines and other applicable regulatory requirements
• Proven ability to work independently in a fast-paced environment
• Strong communication, interpersonal, and organizational skills
• Must demonstrate excellent computer skills
• Must be happy to complete 4-6 visits per month

Responsibilities

• Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
• To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required
• Ensure that all study related communication including e-mail is tracked, printed and filed as required
• The set-up and coordination of Phase I-IV clinical trials across the UK
• To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCR  
• To liaise with all other appropriate departments to ensure the smooth running of the study M
• entor and train other CRA’s as and when required
• Perform document submissions to local authorities

To assemble files and ensure documents for the trial master file accurately reflect the progress of the stud and Other Ad-Hoc CRA duties

Qualifications

• A BSc or BA degree in a life science related field
• Sound knowledge of ICH/GCP and regulatory requirements
• Experience using clinical trial management systems

Background

Details confidential, information available upon request

If you are interested in this vacancy, please contact me on +44 2038759966 or email me on Penny.Melson@upsilonglobal.com