Description
An exciting opportunity for a Clinical Research Associate (CRA) to join an expanding Clinical Research Organisation (CRO) on an initial 6 month contract is now available.This is a home based role where you will be required to monitor between 2-3 days a week.
Some of the key responsibilities include:
-Site monitoring responsibilities for clinical studies according to SOPs, ICH Guidelines and GCP.
-Attend and Participate in investigator meetings.
-Manage study budgets and contracts including negotiations.
-Look after more junior CRAs.
-Identify new investigators for future studies.
-Review CRF's and provide relevant feedback.
-Be the point of contact between the investigation sites and company.
-Assist with IRB/IEC submissions as required. Attend study team meetings.
Required skills and experience:
-Previous Clinical Research/ CRA experience in pharmaceuticals
-In depth knowledge of the ICH Guidelines and GCP
-Proven problem solving capabilities overseeing clinical sites
-Life Science degree
-Motivated and willing to learn
-Effective time management skills
-Work independently
Owing to rapid expansion, this really is an exciting opportunity to work for a leading Pharmaceutical organisation and the chance to open up new opportunities.
The rates are dependent upon candidate experience and I will be able to discuss with you during the application process.
If you are interested in this role please respond ASAP with an updated CV and your location and availability to start and to interview.
Please pass this on to friends or colleagues as we offer referral vouchers.
Thanks and regards,
Keywords: CRA, SCRA, CRA II, CRO, Clinical Research Associate, Monitor, Phase II, Phase III, Pharma, Pharmaceutical, Clinical Trials, SOPs, ICH Guidelines, GCP, Life Science, Contract, Investigator, Budgets, Cardiovascular, CNS.