Clinical Start up Specialist London

Resourcing Life Science; City Of London; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading life science recruitment firm in London is seeking a Start up Specialist to be responsible for CA and Ethics Committee submissions, keeping up to date with GCP and ICH guidelines. The ideal candidate has a bachelor's in life science and at least one year of relevant experience within a CRO, Pharma, or Biotech in the UK. Strong communication skills and fluency in English are required for this role.

Qualifications

• Minimum 1 year in EC & CA submissions within a CRO, Pharma, Biotech in the UK.
• Experience in clinical studies phase II-III.

Responsibilities

• Responsible for CA & Ethics Committee (EC) submission.
• Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
• Translation and coordination of translations for documents required for submissions.
• Supervising study conduct according to GCP requirements and all applicable laws.

Skills

Excellent communication skills

Fluent English

Education

Bachelor degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist office based in London.

Job Overview

• Responsible for CA & Ethics Committee (EC) submission
• Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
• Translation and co-ordination of translations for documents required for submissions.
• Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

• Bachelor degree in life-science
• Min 1 year in EC & CA submissions within a CRO, Pharma, Biotech in UK
• Experience in clinical studies phase II-III
• Excellent communication skills
• Fluent English
• FTE: 1.0