Clinical Data Integrity & Compliance Specialist

Meeveem Limited; Manchester; Hybrid; GBP 28,000 - 38,000; Full time

Job summary

Thermo Fisher Scientific in Manchester is seeking a Data Compliance Coordinator to support UK clinical studies at the local site. You will handle data management, regulatory compliance, and sponsor-site coordination in a fast-paced environment.

The role requires 1 year of clinical research experience, proficiency with eCRF and ISF, and strong English communication. This onsite position offers regular hours and collaboration across a global clinical research team.

Qualifications

• Minimum 1 year of experience in clinical research or data management.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Proficient in eCRF data entry and data query resolution.
• Experience maintaining ISF and study documentation.
• Excellent attention to detail and quality control.
• Strong time management and ability to manage multiple studies.
• Proficiency in Microsoft Office; ability to learn medical terminology.
• Strong English written and verbal communication.
• Ability to travel occasionally.

Responsibilities

• Support the management of UK clinical studies conducted through our Manchester site.
• Act as an operational link between clinical trial sponsors and the research site.
• Work directly with sponsor representatives and clinical research stakeholders.
• Manage and maintain accurate clinical study and patient data.
• Complete electronic Case Report Form (eCRF) data entry and resolve data queries.
• Maintain Investigator Site Files (ISF) and other essential study documentation.
• Coordinate data management and compliance activities across multiple studies.
• Prepare for monitoring visits and support timely follow-up actions.
• Help ensure study activities meet ICH/GCP, regulatory and data protection requirements.
• Perform quality checks to maintain high standards of data accuracy, completeness and integrity.
• Collaborate with colleagues across the site to support an efficient and positive clinical trial experience for participants.

Skills

Attention to detail

Time management

English communication

Education

Clinical Research Certification

Tools

eCRF data entry

ISF management

MS Office

Job description

Thermo Fisher Scientific in Manchester is seeking a Data Compliance Coordinator to support UK clinical studies at the local site. You will handle data management, regulatory compliance, and sponsor-site coordination in a fast-paced environment.

The role requires 1 year of clinical research experience, proficiency with eCRF and ISF, and strong English communication. This onsite position offers regular hours and collaboration across a global clinical research team.