Company: Barrington James Clinical
Closing Date: 04 Nov 16
Salary (£): Competitive
Bored of the same old CRA role? Waiting the progression you've been promised? Looking for some exciting new projects in new emerging companies? Look no further my client are currently one of the top expanding CRO's in the market at the moment and currently have an amazing study pipeline. Mentoring and progression is guaranteed with amazing packages offered. Apply today to be part of a revolution in the clinical research industry!
My client is looking for experienced CRA II’s / SCRAs to join them during this period of exciting growth. Due to several business wins, my client is looking to expand their clinical teams across the business.
These are home and office based roles that are available.
I am looking for candidates who have proven independent, multi-centric monitoring experience.
About the opportunities...
Depending on experience responsibilities include:
All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
All aspects of site and registry management as prescribed in the project plans
Organize and make presentations at Investigator Meetings
Report, write narratives and follow-up on serious adverse events
Review progress of projects and initiate appropriate actions to achieve target objectives
You may serve as lead monitor for a protocol or project and assist in establishing monitoring plans if required
Participate in the development of protocols and Case Report Forms as assigned
Interact with internal work groups to evaluate needs, resources and timelines
Education/Qualifications Typically required:
University/college degree (life science preferred), or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology).
Alternatively, candidates with two or more years of relevant clinical research experience in pharmaceutical or CRO industries will also be considered
Experience Typically required:
Clinical research monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) preferably in a CRO or Pharma environment
Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines
Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Good knowledge of ICH Guidelines and GCP, monitoring procedures and understanding of the clinical trial process
Good planning, organization and problem solving abilities
Good communication and interpersonal skills
This role offers a very clear career progression with amazing training schemes in place to get you to fast track your clinical career! With an amazing culture and family feel this company is renowned for their work atmosphere and has been voted one of the best companies to work for in 2015! Not only this but this comapny have the lowest retention rate of any company globally within the indursty! Act now and apply
If you feel you would be the right person for this job or know anyone who you believe this would be ideal for please contact me on 01293 776644 or email me on firstname.lastname@example.org
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