Job Description

Job Title Ref: BBBH30401_1689666501

Senior CRA II

Salary 45000.00 - 70000 GBP

Location

England

2023-07-18

2023-08-15

Type Permanent

Sector Drug Development

i-Pharm https://www.i-pharmconsulting.com/

Senior Clinical Research Associate

Location: UK remote

Salary: Flexible & Competitive

Ask yourself this:\xc3\xa2\xc2\x80\xc2\x8b

• Are you ready for a company that prioritises you and your development?
• This is Including a fair and competitive salary that reflects your value to the business?\xc3\xa2\xc2\x80\xc2\x8b
• Annual performance reviews that show value and commitment to your career progression?
• Looking for a friendly and supportive leadership team?
• Looking for variety in your work, a large company that can offer this?

If the answers to the above is YES then we think we\'ve the right company for you!\xc3\xa2\xc2\x80\xc2\x8b

\xc3\xa2\xc2\x80\xc2\x8b

The Job:\xc3\xa2\xc2\x80\xc2\x8b

I\'ve partnered with a leading global CRO where their Clinical Operations department is looking to hire a Senior CRA to work mainly on complex Oncology trials. You can be based anywhere in the UK

The studies run across a wide range of therapy areas, helping you to build and develop your therapeutic knowledge base! Working with many sponsors from large pharmaceutical companies to small biotechnology companies - across all phases of drug development.

• National monitoring across the UK
• Studies will be 90% Oncology, so complex protocols
• ONC trials will include various solid tumour studies, Prostate, NSCLC, Leukemia, Breast, Glioblastoma and studies in Hematological malignancies.
• Other TAs include Respiratory, Cardiovascular, Infectious disease, Nephrology, Endocrinology, & Gastroenterology.
• On average each CRA will work across 5-6 Protocols (3-4 OCN plus \\"something else\\")
• Risk based monitoring model
• Min of 8 days on site per month

Why this opportunity?

• You\'ll have a strong support team of in-house CRA\'s which give you more time to focus on your own development
• Career Progression - development and progression is a huge focus within my client
• Routes in to Line Management, Clinical Trial Manager, Quality Assurance
• Movement into FSP (client dedicated roles) and Clinical Pharmacology (1st in man trials)
• Our Line Managers are warm and open individuals who have a flexible and supportive approach.

Experience

• At least 4 year of previous monitoring experience within the UK.
• Experience in working on Oncology trails in phase II & III
• Have an understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Ability to train and supervise junior staff
• Ability to resolve project-related problems and prioritizes workload for self and team
• Ability to work within a project team
• Valid Driver\'s License

\xc3\xa2\xc2\x80\xc2\x8b To Apply:

Send your CV to me, Clara Burke at cburke@i-pharmconsulting.com or call me on 020 7551 0723 for a confidential chat.

Apply for this job

Clara Burke

Contact me about this role

i-Pharm Consulting