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Senior Clinical Scientist

  1. Poland, UK
2024-108765
  1. ICON Strategic Solutions
  2. Clinical Trial Management

About the role

This vacancy has now expired. Please click here to view live vacancies.

As a Senior Clinical Scientist you will be supporting a global mid-sized biotech company. While being stably employed with ICON, you will be fully embedded with our client.

 

 

 


Job Summary:

Senior Clinical Scientist is responsible for working with the physicians within Clinical to provide clinical research support for programs as assigned by phase or therapeutic area.

 

Responsibilities:

  • Preparation of clinical development plans
  • Drafting of clinical scientific documents such as IND, IND amendments, IBs, Annual reports
  • SAE reconciliation 
  • Monitor, review and summarize safety and efficacy of data in ongoing studies
  • Review tables and listings
  • Work with various databases reviewing patient profiles, posting queries
  • Lead the clinical matrix teams for assigned compounds
  • Represent exploratory development on project teams

Qualifications:

  • Degree in scientific/life-sciences field Pharm.D. or Ph.D. preferred
  • Minimum 4-6 of experience as a clinical scientist or research with at least 3 years of drug development experience are required
  • Data review/cleaning (patient by patient review and review of listings)/Query writing
  • Experience in monitor, review and summarize safety and efficacy data in ongoing studies
  • Prior Oncology Drug Development experience is a plus
  • Strong Analytical ability
List #1

Day in the life

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How to excel as a CRA in a Clinical Research Organisation

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Our People

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Publish date

08/29/2023

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

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Publish date

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Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan

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In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe

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In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics. This is subject to change with an increase in decentralised clinical trials (DCTs).

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