United BioSource Corporation.

Sr Clinical Research Associate - Home based

Expiring today

London, United Kingdom
19 Sep 2019
19 Oct 2019
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Brief Description: Monitors in accordance with ICH, GCP, CFR guidelines, UBC and project SOPs

Supervisory Responsibilities: Mentoring new and/or junior CRAs

UBC are looking for a CRA/SCRA with at least 2 years monitoring experience in the UK. You may be working on late phase studies, clinical trials or a combination of both. Ideally, we are looking for someone with experience in oncology and late phase studies but this is not essential.

At UBC you will also be directly involved in site contract and budget negotiations. This is a great opportunity for a CRA from a large CRO background to gain new skills if you have no previous experience.

Location is flexible - you can be office based in Hammersmith with the option for working from home 2 days per week - we will also consider home based if you live further afield.

If you are looking to gain new skills and exposure to other phases with reduced travel, UBC may be just the place for you!

  • Bachelor's degree - Life Science preferred or equivalent years of industry and monitoring experience
  • At least 2 years active monitoring in the UK
  • Experience in electronic CTMS, EDC, eTMF
  • Minimum travel - approximately 20% depending on study allocation

Specific Job Duties:
  • Thorough knowledge of UK legislation applicable to clinical trials/ observational studies and ICH GCP.
  • On site / remote monitoring visits
  • May be required to support / mentor junior CRAs
  • Preparation, submission and tracking of local ethics committee and other regulatory applications
  • Contract and budget negotiation with hospitals and local R&D Departments
  • Study feasibility assessments where required



United BioSource Corporation (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our services support the full lifecycle of medicine and medical products, including development, commercialization, and long-term value and safety.

While UBC offers employment within Patient Support, Nursing, Pharmacy and Corporate, two main focus areas for the company are Clinical Development & Research and Safety & Risk Management. Members of the Clinical Development and Research teams help evaluate study protocol, target study population, recruit physicians and patients, and collect, clean, validate and report data. As a result, sponsors are able to submit findings to regulatory authorities or make a no-go decision in a timely and clear-cut manner. Additionally, our Safety and Risk Management teams develop, deliver, and report evidence to reinforce safe and appropriate product use.

Through our Patient Access services, we help patients begin therapy quickly and remain on therapy, building strong relationships with patients to ensure optimal care.
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