Rota and Clinical Coordinator

Montu UK; Wendy; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading cannabis company in the UK is seeking a Clinical Registry Administrator to provide oversight and accountability for clinical trials. This role involves collaboration with various partners to ensure successful registry submissions and to maintain data integrity throughout the disclosure process. Candidates should have a bachelor's degree in health or science and a minimum of four years of relevant experience in clinical research. A proactive approach and leadership skills are essential for success in this role.

Qualifications

• Minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment.
• Clinical Registry experience preferred.
• Experience working on a clinical trial or regulatory document management preferred.

Responsibilities

• Provides support and oversight for clinical trials.
• Takes leadership role with internal and external partners.
• Responsible for submission of documents to registries.
• Tracks and documents disclosure records.

Skills

Clinical research

Data management

Leadership

Regulatory compliance

Education

Bachelor's degree in Health or Science discipline

Job description

Clinical Registry Administrator

• Provides clinical registry support, oversight, and/or accountability for one or more development programs for clinical trials.
• Takes a leadership role with the clinical development team and other internal and external partners to establish, align, and confirm clinical registry expectations for assigned trial(s).
• Responsible for submission of approved documents and content to registries worldwide. Submissions are made by the Clinical Registry Administrators.
• Responsible for tracking, reporting, and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group.
• Assists business partners, external partners, and local operating companies in maintaining accurate and correct (source) data relevant to the disclosure process.
• Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning.
• Ensures deliverables are on time.

Clinical Registry Administrator role: Provides clinical registry support, oversight and/or accountability for one or more clinical trials. Gathers content and integration requirements for registration records - Establishes expectations for dataset content and structure.

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Qualifications

• A minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO, or other clinical development service organization) is required.
• Bachelor's degree in Health or Science discipline is required with experience in clinical research
• Clinical Registry experience preferred.
• Experience working on a clinical trial or regulatory document management preferred.

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

About Montu

About Us Montu is the UK's leading cannabis company, transforming the patient journey through technology and clinical excellence. We are committed to providing safe, accessible, and high-quality medical cannabis care to improve the lives of patients across the country.