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 Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch

Providing Flexible Resourcing Solutions CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in

Basel, London 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 one of our clients, we are currently looking for a

Clinical Research Associates Reference Number: 50-13-824-CRA-W Type of placement: Permanent Location: Field Based (UK) Our client is the word’s leading provider of biopharmaceutical services. With a network of > 27,000 professionals working in over 80 countries, it has helped develop or commercialise all of the top 50 best selling drugs on the market. Through its application of extensive therapeutic, scientific and analytical expertise, our client helps biopharmaceutical and health sciences customers navigate the increasingly complex landscape with more predictability to enable better outcomes. 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 more less experienced clinical staff. Qualifications and Experience:

Bachelor's degree in a health care or other scientific discipline, no less than1 year of on-site monitoring experience; or equivalent combination of education, training and experience

Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines

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

Effective time management skills

Ability to manage competing priorities

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 Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch

Ability to establish and maintain effective working relationships with co-workers, managers and clients

Our offer:

Competitive basic salary

Company Car

Bonus Flexible benefits package including, but not limited to:

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