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Freelance Clinical Research Associate

Employer
Barrington James
Location
Multiple Locations
Salary
Negotiable
Start date
8 Jun 2022
Closing date
8 Jul 2022

View more

Discipline
Clinical Research, Clinical Operations
Hours
Part Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

Job Details

Clinical Research Associate - Contract 

My client is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, they advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

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

The Role

The culture is centered around support, growth and development and a drive to innovate.

Its Biotech Solutions offers CRAs the opportunity to gain a wide range of therapeutic experience and to work within an open and transparent environment with a focus on offering a flexible and adaptable mindset and approach to make the client’s needs.

Its Biotech Solutions Clinical Delivery team is world-class and offers huge opportunities for career growth and development through our internal training programs, ongoing mentoring and employee reward and recognition schemes.

Clinical Research Associates are ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. My client offers a broad therapeutic disease portfolio giving you opportunities to work on studies in areas such as Paediatrics, Rare diseases and Gene Therapy.

Key responsibilities include:

  • Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
  • Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
  • Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
  • Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following up on drug safety issues.
  • Ensuring the integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

You will be operating as a key part of a global study team and plays a fundamental role in their clients’ drug development processes.

The Requirements

  • Prior experience working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
  • Working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
  • You will be educated to a degree level

Hourly/daily rate negotiable depending on experience. 

Easily apply now with a click of a button!

Company

We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Company info
Website
Telephone
01293 776644
Location
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
GB

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