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SCRA –Bristol – £10,000 sign up bonus
Resourcing Life Science
Bristol
On-site
GBP 30,000 - 60,000
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Job summary
Join a forward-thinking global CRO as a Clinical Research Associate based in Bristol! This exciting role involves monitoring clinical studies and ensuring adherence to Good Clinical Practices. With a focus on phases II-III, you will play a crucial role in the success of clinical trials while collaborating with top-tier pharmaceutical and biotech companies. The position offers a £10,000 welcome bonus for applicants this month, making it an excellent opportunity for those looking to advance their careers in clinical research. If you are passionate about life sciences and have the required experience, this could be the perfect fit for you.
Benefits
£10,000 welcome bonus
Qualifications
- 1.5+ years of monitoring experience in a CRO, Pharma, or Biotech.
- Strong understanding of GCP and clinical study phases II-III.
Responsibilities
- Monitor clinical studies and ensure compliance with GCP and regulations.
- Identify and initiate investigators and their sites for studies.
Skills
Monitoring clinical studies
Good Clinical Practices (GCP)
Excellent communication skills
Site initiation and close out
Fluent English
Education
Bachelor degree in life-science
Job 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 Clinical Research Associate home based in Bristol. There is a £10,000 welcome bonus for colleagues who are applying this month.
- Monitoring clinical studies in phases II-III
- Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
- Identification, qualification and initiation of investigators and their sites.
- Supervising study conduct according to GCP requirements and all applicable laws.
- Bachelor degree in life-science
- Min 1.5 year monitoring experience as CRA within a CRO, Pharma, Biotech
- Experience in commercial studies
- Experience with site initiation, site close out
- Experience in clinical studies phase II-III
- Fluent English
- Excellent communication skills
- A full clean drivers license
- FTE: 1.0
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