ICON Clinical Research

Senior Site Management Associate

Location
Manchester,marlow,reading
Salary
Competitive
Posted
23 Jul 2021
Closes
21 Aug 2021
Ref
JR076723
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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.

The (Senior) Site Management Associate is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations. This would be a great opportunity for someone with experience of onsite monitoring experience looking to broaden their skills and experience OR for experienced CRA's looking to travel less and discover the opportunities of late phase research. The position can be home based in the UK,

The Role:

The responsibilities of this position include, but are not limited to:
  • Identifying, training/initiating and closing out study sites
  • Performing submissions to Ethics Committees and Regulatory authorities as applicable
  • Conducting remote and onsite monitoring visits in the UK.
  • Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.


What you'll need to be successful in the role:
  • A Bachelor's degree in the life sciences,
  • Expertise with regulatory guidelines and clinical terminology, and
  • Demonstrable strong site management experience will ensure your success on our team.
  • We would also welcome some prior Study Start Up experience ie study feasibility, site identification, ethics committee and regulatory authority submissions, contract negotiations, site activation.


Benefits of Working in ICON:

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. 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 through the form below.