Field based - South East
Regional CRA for a Top 10 Pharmaceutical Company
Apply Now for this 5 month Contract, great team and project scope.
Good Pay Rate £££
Regional^CRA position home based, ideally in the South East of England. You will be supporting project teams in the feasibility, start up, conduct and monitoring of both pivotal and supportive clinical trials across the UK. This is a role with a leading pharmaceutical company team, you will be home based and involved with studies in key disease areas, you may be working across protocols and at times be required to offer some leadership support at country level.
You could be involved in studies in Phases I-IV. The roles involve you in working in an environment of best practice where quality of relationship, passion for your work and professionalism is rewarded well.
To apply you must be ready to set up a home office facility, a mobile phone and you will need a car for business use. The company uses EDC so proficiency in working with this at sites and remote Fit for Purpose Monitoring practices is desirable.
Essential Skills & Qualification
Relevant experienced as a UK CRA with ability to initiate and monitor hospital studies
Experience across more than one Phase of study
Therapy area experience
Excellent interpersonal skills are essential
Ability to prioritise and manage multiple tasks with conflicting deadlines
Candidates must be able to work independently as well as in a team environment
All candidates must be prepared to travel to sites out of their local region
Self motivated and proactive
Can travel throughout the UK as required
Attend UK based team meetings held monthly
Occasional overnight stays required
Candidate must have own transport and home office and mobile
Software Competence: MS Office, MS Project, INFORM or RAVE, IMPACT
Valid Driving License: Essential
Working Language(s): English
Requirement for Business Travel: Yes
Flexible Working Hours: No
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 5 Months
Location:^UK; Location Independent, South England
Plan Start Date: ASAP
Contract Benefits: Day Rate inclusive of benefits
MS Office,INFORM, IMPACT, RAVE , Medical Affairs, KOL, publications, IIS, Late Phase, lifecycle, Clinical Research, Clinical Operations, Clinical R&D, CRA, CTM, CTA, GCP, Site Manager, Monitor, Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility , Essential Documents, GCP, SOPs, Compliance, Training, Investigator Meeting, REC, Research Ethics. R&D, Trust, SMO, Site Manager, Quality Control, QC, EDC
Assigned Consultant: Matthew Pike at CSL Recruitment on 01932 234 685
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs, applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate.