Senior Clinical Data Manager

Clearline Recruitment Ltd; Welwyn Garden City; Hybrid; GBP 52,000 - 72,000; Full time

Benefits offered by this job

Hybrid working 2–3 days in office

25 days holiday + Bank Holidays

Free on-site parking

Job summary

Clearline Recruitment Ltd in Welwyn Garden City is seeking a Senior Clinical Data Manager to oversee end-to-end data management across clinical studies. You will lead CRF design, data specifications, and query resolution while collaborating with Biostatistics and Clinical Operations teams.

The role is hybrid, 2-3 days in the office, full-time on a 6-month Outside IR35 contract. Candidates should have 5+ years in data management or 3+ years with an advanced degree, and strong EDC/CDISC experience.

Qualifications

• Minimum 5 years of clinical data management experience, or 3 years with an advanced degree.
• Bachelor's or Master's degree in Life Sciences, Computer Science, Statistics, Informatics or a related discipline
• Hands-on experience managing data for clinical trials
• Experience with CRF design and query resolution
• Working knowledge of EDC systems and data standards such as CDISC
• Understanding of clinical data types and their relation to analysis
• Familiarity with risk-based monitoring or data quality metrics
• Ability to work independently and manage multiple priorities
• SAS, R or Python knowledge would be advantageous
• Early-phase or adaptive study experience would be beneficial

Responsibilities

• Independently manage end-to-end data management across one or more clinical studies
• Oversee activities from CRF and database design through to final study closure
• Work with Biostatistics, Data Science and Clinical teams to define data specifications
• Support the selection and oversight of data-related vendors
• Drive timely data entry and query resolution
• Resolve complex clinical data issues across systems including EDC, ePRO and IRT
• Review and improve study-level data processes
• Ensure third-party vendor deliverables meet regulatory and quality requirements
• Support high-quality data delivery and readiness for analysis
• Share technical expertise and contribute to continuous improvement across the wider team

Skills

Clinical data management

CRF design

Query resolution

Independent work

Education

Bachelor's or Master's in Life Sciences/CS/Statistics/Informatics or related

Tools

EDC systems

CDISC data standards

SAS

R

Python

Job description

Role: Senior Clinical Data Manager

Location: Welwyn Garden City, Hybrid - 2-3 days per week in the office

Hours: Full-time

Contract: 6 months, Outside IR35

Pay: £37.76 - £42.28 per hour PAYE basic excluding holiday pay or £50 - £56 per hour LTD/Umbrella

An excellent opportunity has arisen for a Senior Clinical Data Manager to join one of our longstanding clients, a leading global healthcare organisation, in Welwyn Garden City.

This is a senior clinical data management position responsible for ensuring the quality, integrity and availability of clinical trial data across one or more studies, working closely with Biostatistics, Data Science, Clinical Operations and other cross-functional teams.

Benefits:

• 25 days holiday plus Bank Holidays
• Hybrid working, with 2-3 days per week in the office
• Free on-site parking
• 6-month contract, Outside IR35
• Opportunity to work within a leading global healthcare organisation
• Exposure to global clinical trials and innovative data technologies

The Requirements:

• Minimum 5 years' clinical data management experience, or an advanced degree with 3 years' equivalent experience
• Bachelor's or Master's degree in Life Sciences, Computer Science, Statistics, Informatics or a related discipline
• Hands-on experience managing data for clinical trials
• Experience with CRF design and query resolution
• Working knowledge of EDC systems and data standards such as CDISC
• Good understanding of clinical data types and how they relate to analysis
• Familiarity with risk-based monitoring or data quality metrics
• Ability to work independently and manage multiple priorities
• SAS, R or Python knowledge would be advantageous
• Early-phase or adaptive study experience would be beneficial

The Role:

• Independently manage end-to-end data management across one or more clinical studies
• Oversee activities from CRF and database design through to final study closure
• Work with Biostatistics, Data Science and Clinical teams to define data specifications
• Support the selection and oversight of data-related vendors
• Drive timely data entry and query resolution
• Resolve complex clinical data issues across systems including EDC, ePRO and IRT
• Review and improve study-level data processes
• Ensure third-party vendor deliverables meet regulatory and quality requirements
• Support high-quality data delivery and readiness for analysis
• Share technical expertise and contribute to continuous improvement across the wider team