1. Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded 1997, is a pan-European specialist staffing organisation with
offices in London, Basel and Munich, providing flexible resourcing solutions to the pharmaceutical
industry across Europe, with contract and permanent placements in clinical development, data
management, statistics, regulatory affairs and medical marketing
For a key client, we are currently looking for a:
CRA / Senior CRA
Reference Number:
Type of placement:
Location:
893298-W
Permanent
Field Based (UK)
Are you an experienced CRA with a desire to work with one of the world’s largest pharmaceutical
companies? Would you like to work on pivotal oncology trials in support of the registration of
breakthrough cancer treatments in the UK? Our client is a global CRO with an exclusive partnership
with a top-10 pharmaceutical company. With a late phase trial starting in Q1 2014, its goal is to
establish a dedicated UK-based clinical operations team to perform start-up, management and closeout of critical studies. This is a unique, permanent opportunity to join a rapidly growing business unit
and benefit from expertise from both organisations.
Main Responsibilities:
 Perform site selection, initiation, monitoring and close-out visits in accordance with contracted
scope of work and good clinical practice.
 Provide monitoring visits and site management for a variety of protocols, sites and therapeutic
areas.
 Administer protocol and related study training to assigned sites and establish regular lines of
communication with sites to manage on-going project expectations and issues.
 Evaluate the quality and integrity of study site practices related to the proper conduct of the
protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead
(CTL) and/or line manager.
 Manage the progress of assigned studies by tracking regulatory submissions and approvals,
recruitment and enrolment, Case Report Form (CRF) completion and submission, and data
query generation and resolution.
 Create and maintain appropriate documentation regarding site management, monitoring visit
findings and action plans by submitting regular visit reports and other required study
documentation.
 May provide assistance to less experienced clinical staff.
Qualifications and Experience:
 Bachelor's degree in a health care or other scientific discipline
 At least one years on-site monitoring experience
 Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements;
i.e. ICH/GCP
 In depth therapeutic and protocol knowledge as provided in company training
 Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of
a laptop computer
 Strong written and verbal communication skills including good command of English language
 Excellent organizational and problem-solving skills

2. Our offer:
 Competitive basic salary
 Company Car
 Bonus
Flexible benefits package including, but not limited to:
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Contributory Pension
Private Health Insurance
Permanent Health Insurance
Life Assurance
Additional benefits based on health and well-being
25 days holiday increasing with length of service
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Resourcing Solutions, 117 Waterloo Road, SE1 8UL, London, UK
Tel.: +44 207 193 9972
www.ctcon.ch
info@ctcon.ch