Clinical Data Manager
| Dyddiad hysbysebu: | 30 Gorffennaf 2025 |
|---|---|
| Cyflog: | £45,000 i £50,000 bob blwyddyn |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 29 Awst 2025 |
| Lleoliad: | Sale, Greater Manchester |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | CHANDRAWAR IT TECHNOLOGIES PVT LTD |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: |
Crynodeb
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)
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)