Job expirat
Our client one of the largest pharmaceutical companies in the world is looking for an experienced office based CRA for a 12 months contract, most likely to extend the contract. The core requirements include study monitoring in line with ICH GCP and SOP's including verification of source documentation and reporting of adverse effects. Continuous development of relevant therapeutic area knowledge
Preparation of timely reports detailing studying site activities
Life science degree
At least 2 years experience as a Clincal Research Associate/Monitor in a Contract Research Organization or pharmaceutical company
Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team
Good communication skills
Prepared to travel locally and internationally
Fluency in English, both written and spoken
Attractive compensation package with benefits
A new challenge and prospects of career progression within a growing company
A high level of responsability and independence
A supportive, friendly working environment
For further information or applications please email alina.lapadatu@hayspharma.com
Hays Pharma is a leading global pharmaceutical and biotech staffing business that provides mid to upper level staff involved in drug discovery, clinical development, post-approval services and commercial activities.
Our client portfolio spans the world\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'s leading life sciences companies in the pharmaceutical, biotechnology, generics, CRO and medical device industries. These organisations have come to depend on our professional service, innovative solutions and global reach.
With 21 offices around the world and over 350 people working through Hays Pharma and a global database of pharmaceutical professionals, we will successfully search and place over 1,000 pharmaceutical & biotech professionals this year. Hays Pharma provide the staff that help maximize returns on R&D investments and accelerate the delivery of safe and effective therapeutics to patients.