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CTA Cambridge UK Cambridgeshire

ICON plc

Full Time Cambridgeshire 10.56 - 12.04 GBP Today

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well

CTA office-based in Cambridge

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance to join us as a CTA.

You will have the opportunity to join a well-established team of dedicated CTAs working on exciting clinical trials

The ideal candidates will bring clinical trials administration skills with the ability to multi-task and work within a close-knit team.

Key Activities:

Responsible for study start-up activities, including creating site folders, collating, preparing and maintaining (e) SIP documents, updating systems

Liaise with clinical sites to collect, review and track feasibility questionnaires
Co-ordinates entry and maintain local data into study management systems (eClinical, CDSS/CDSSR, SADMS, etc.) including setting up new studies in eClinical
Act as a back-up for other Supplier CTAs
Ensures collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including when appropriate preparation and submission of all documents to the central and/or local committee
Track and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders, study drugs and Site Initiation presentations/materials
Orders, processes and tracks Case Report Forms (CRF) and follows up on query resolution if required to do so
Manage local distribution of Investigator Brochure
Prepare and review site communication documents; facilitate mass mailings/faxes
Provide administrative support such as word processing, photocopying, faxing, filing, managing correspondence, presentations preparation, basic computer software support

Full job details on request

Responsibilities:

Interacts with Clinical Research Services Manager for project or study related work
Supports the execution of clinical studies
Responsible for study start up activities
Tracks study related documents
Manages logistics and document exchange between clinical sites and the company
Actively contributes to results oriented department goals
Drives continuous improvement of GCSM
Promotes operational and scientific excellence within local GCSM
Identifies opportunities and best practices with local and regional partners that will contribute to overall operational effectiveness

What is Offered

Office-based in the Cambridge office
Full-time
Salary will be offered depending on level of experience and skills
Permanent contract of employment 100% dedicated to 1 single sponsor with company benefits

What is required:

Ideally BA/BS/BSc or qualified nurse
UK-based clinical trial co-ordination/administration experience gained within the clinical research industry or within NHS trust/hospital setting
Proven ability to work efficiently and accurately with MS Office and EDC systems
Ability to work effectively to fast-moving timelines within a fast-paced working environment using different electronic systems
Excellent and accurate attention to detail when entering data onto systems/database
Valid, current UK working eligibility

Please contact me with your most recent CV today!

Benefits of Working in ICON:

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

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