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Job Details
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Clinical Research Associate - Single Sponsor



Business Type: Pharmaceutical Company, Clinical Research Organisation
Job Type: Clinical Research Associate (CRA), Senior Clinical Research Associate (SCRA)
Job Level: Experienced (non manager)
Position: Full Time
Location: United Kingdom
Reference: CNOB630
Closing Date: 18/01/19
Job Details:

JOB SUMMARY

This leading international CRO is seeking an experienced CRA who has worked on complex studies across a broad range of therapeutic areas, including but not limited to, Oncology, Rare Diseases, Neurology, Autoimmune Diseases and Diabetes. This position is home based in the UK. This is an excellent opportunity for CRAs with 1.5+ years'' experience to work with a global CRO with clear career development and growth. This CRO partners with leading drug development companies, and you''d be working with one single sponsor.

LOCATION

United Kingdom, UK, Home-based

ROLE/DESCRIPTION

You''ll have 1.5+ years'' experience working as a clinical research associate in varying therapeutic areas including Oncology. You''ll have previous experience working in a pharmaceutical environment or worked as a CRA in a CRO. You''ll have knowledge of, and skill in applying, applicable research regulatory requirements (Good Clinical Practice, and International Conference on Harmonisation guidelines). You will also have a sound understanding of the drug development process.

You will be working with a global leading pharmaceutical company where you will perform independent monitoring for differing Oncology studies. This position will require you to be responsible for the independent pre-study initiation, routine monitoring and close out visits. You will also be required to aid in the production of clinical trial related materials and documents.

COMPANY

This CRO is a dynamic leader within the pharmaceutical industry, with progression and career development high on their list of priorities. The company has a network of 1,000+ employees operating in over 50 countries worldwide. Trials are ongoing in a broad range of therapeutic areas, including but not limited to: Oncology, Rare Diseases, Neurology, Autoimmune Diseases and Diabetes.

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 1.5 years independent monitoring experience
  • Experience working in a range of therapeutic areas including Oncology
  • Entitlement to work in the UK
  • Full UK Driver''s License
  • Sound presentation and communication skills.

BENEFITS

  • Excellent Salary
  • Car or car allowance
  • Healthcare
  • 25 days'' annual leave
  • Pension
  • Flexi Benefits

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Principle Consultant Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.com. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

CRA / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / ICH / Oncology / Neurology/ Diabetes / Autoimmune Diseases/ Rare Diseases / England / Scotland / CRO / Contract Research Organisation / Pharmaceutical /Single Sponsor / Home Based / Outsourcing



Posted: 11/01/2019 | NPJ Ref: 228396
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