Clinical Registry Lead for Trial Submissions

IQVIA; Reading; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading global clinical research provider is seeking an individual with a strong background in clinical development to provide registry support and oversight. The ideal candidate will have a minimum of 4 years of experience in a pharmaceutical or clinical environment, along with a relevant Bachelor's degree. Responsibilities include leading the clinical development team, ensuring compliance, and maintaining accurate data for clinical trials. This position offers the opportunity to contribute to the advancement of innovative medical treatments.

Qualifications

• Minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment.
• Experience in clinical research is required.
• Clinical Registry experience is preferred.

Responsibilities

• Provide clinical registry support and oversight for development programs.
• Lead the clinical development team to establish clinical registry expectations.
• Track and report disclosure records and associated documents.

Skills

Clinical development experience

Data accuracy maintenance

Project management

Leadership skills

Education

Bachelor’s degree in Health or Science

Job description

A leading global clinical research provider is seeking an individual with a strong background in clinical development to provide registry support and oversight. The ideal candidate will have a minimum of 4 years of experience in a pharmaceutical or clinical environment, along with a relevant Bachelor's degree. Responsibilities include leading the clinical development team, ensuring compliance, and maintaining accurate data for clinical trials. This position offers the opportunity to contribute to the advancement of innovative medical treatments.