Clinical Data Manager

www.findapprenticeship.service.gov.uk - Jobboard; Sale; On-site; GBP 47,000 - 61,000; Full time

Job summary

A leading job board for apprenticeships is seeking a Data Manager to oversee the collection and management of clinical trial data. The ideal candidate will ensure data integrity, compliance with industry standards, and collaborate with various teams in a dynamic environment. This full-time position offers a competitive salary and opportunities for professional growth.

Benefits

Competitive salary

Opportunity for professional growth

Qualifications

• Minimum 3 years of experience in clinical data management, preferably in pharmaceutical or CRO settings.
• Must have strong knowledge of clinical trial data processes and regulatory requirements.
• Ability to train and guide junior data management staff as needed.

Responsibilities

• Develop and maintain data management plans, study-specific CRFs, and databases for clinical trials.
• Oversee data collection, entry, validation, and cleaning processes to ensure data integrity.
• Collaborate with cross-functional teams including clinical operations and SAS programmers.

Skills

Attention to detail

Problem-solving skills

Organisational skills

Communication skills

Education

Bachelor’s degree in Life Sciences, Computer Science or related field

Tools

Clinical trial data processes

CDISC standards (SDTM, ADaM)

EDC systems

SAS programming

Job description

Job Summary

We are seeking a detail-oriented and experienced Data Manager to join our dynamic team. The ideal candidate will oversee the collection, validation, and management of clinical trial data, ensuring accuracy, completeness, and compliance with industry standards and regulations. This role will involve close collaboration with clinical teams, statisticians, SAS programmers, and project managers.

Key Responsibilities

Develop and maintain data management plans, study-specific CRFs, and databases for clinical trials.
Oversee data collection, entry, validation, and cleaning processes to ensure data integrity.
Manage database design, including building and testing data collection systems.
Collaborate with cross-functional teams including clinical operations, biostatistics, and SAS programmers.
Monitor data queries and resolve discrepancies in a timely manner.
Ensure compliance with regulatory standards (e.g., GCP, FDA, EMA) and SOPs.
Prepare data for analysis and support data transfer to SAS programming teams.
Generate data management reports and documentation throughout the study lifecycle.
Train and guide junior data management staff as needed.

Qualifications

Bachelor’s degree in Life Sciences, Computer Science, or related field.
Minimum 3 years of experience in clinical data management, preferably in pharmaceutical or CRO settings.
Strong knowledge of clinical trial data processes, CDISC standards (SDTM, ADaM), and EDC systems.
Experience with SAS programming or close collaboration with SAS teams is a plus.
Excellent attention to detail and problem-solving skills.
Strong organisational and communication skills.
Familiarity with regulatory requirements and quality standards in clinical research.

Why Join Us?

Work with a passionate team supporting cutting-edge clinical research globally.
Opportunity to grow your expertise in SAS and clinical data management.
Competitive salary and benefits.

Job Type: Full-time

Pay: £47,420.00-£60,934.11 per year

Schedule:
Monday to Friday

Ability to commute/relocate:
Sale M33: reliably commute or plan to relocate before starting work (preferred)