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The Opportunity: In this role, you will lead daily clinical coding operations and data quality initiatives within an NHS setting. You will supervise and mentor clinical coders, perform accurate ICD-10 and OPCS-4 coding, and resolve data quality issues to support financial flows and operational requirements.

Your Impact

• Coding & Data Quality: Extract and record complex clinical data using ICD-10 and click apply for full job details

Talentmark are recruiting for a Senior Data Manager to join a company in the pharmaceutical industry on a contract basis for 6 months. This role is a hybrid role with 2 or 3 days per week on-site in Welwyn Garden City.

Company:
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Salary:
37.76 - 42.28 PAYE or 50 - 56 via umbrella or Ltd. This role is outside IR35.

Senior Data Manager Role:

• Independently manage end-to-end data management activities for one or more studies, from CRF and database design to final study closure.
• Collaborate with cross-functional partners (Biostats, Data Science, Clinical) to define data specifications and ensure data meets study needs.
• Resolve complex data issues using industry best practices, knowledge of risk-based monitoring, and system capabilities.
• Support oversight of third-party vendors to ensure data deliverables meet regulatory and quality expectations.
• Lead the design, implementation, and oversight of data management activities across one or more studies.

• Hold a relevant degree or have equivalent working experience.
• Extensive experience in clinical data management or a related function.
• hands-on experience managing data for clinical trials (e.g., CRF design, query resolution).
• Hands-on experience managing data for clinical trials (e.g., CRF design, query resolution)
• Programming literacy (e.g., SAS, R, Python) for data review or visualization

Data ManagerLocation: Cambridge (Hybrid, 2 days in the office)
Salary: 40,000 to 48,000
Contract: Permanent, full-time
I'm working with an innovative life sciences and clinical research technology business based just outside Cambridge that is looking to bring on a Data Manager to join its growing Data Management team.
The business develops digital technologies and assessments used in clinical trials, helping researchers better understand patient symptoms and supporting the development of new treatments. With an established presence internationally and over 30 years of scientific expertise behind its work, this is an opportunity to join an organisation where data quality directly contributes to clinical research and healthcare outcomes.
The RoleYou'll take ownership of data management activities across a portfolio of clinical studies, working from study initiation through to database lock and final data transfer. Alongside the technical responsibilities, you'll act as a key point of contact for clients, ensuring data quality, transparency and reliable delivery throughout the study lifecycle.
This is an opportunity for someone who enjoys getting into the detail of data, investigating discrepancies and improving existing processes, rather than simply following established procedures. The team is particularly interested in someone who is curious about new technologies, including AI, and is keen to identify more efficient and effective ways of working.
Key Responsibilities

• Manage clinical data activities across multiple studies, from initial setup through to database lock and final data delivery.
• Act as the primary data management contact for clients, building strong relationships and communicating progress, risks and priorities.
• Develop and maintain Data Management Plans, Data Transfer Agreements and documentation in line with GCP requirements.
• Undertake data cleaning, query management and reconciliation, investigating discrepancies and ensuring data integrity.
• Configure, test and manage data transfers, including developing production code and quality control processes.
• Produce bespoke client reports and data extracts using ETL tools.
• Estimate project timelines and costs, managing deliverables against agreed SLAs.
• Support audits and regulatory inspections, ensuring data management processes and documentation meet the required standards.
• Identify opportunities to improve existing SOPs, workflows and data management practices.
• Collaborate with clinical scientists, statisticians, project managers and external stakeholders to ensure successful study delivery.

• Experience in a Clinical Data Manager, Clinical Data Coordinator or similar role within a clinical trial environment.
• Practical experience using Electronic Data Capture (EDC) systems.
• Understanding of ICH-GCP principles and clinical data management practices.
• Basic programming skills in Python, SQL, SAS, R or a similar language.
• An interest in using AI to support data analysis and improve workflows, alongside the ability to learn new tools quickly.
• An understanding of clinical trials and the drug development lifecycle, or a genuine interest in clinical research.
• Strong attention to detail, analytical thinking and root-cause investigation skills.
• Experience maintaining data quality records and documentation to GCP standards.
• The ability to manage multiple studies, competing deadlines and changing priorities.
• Strong communication skills and confidence working directly with clients.
• A proactive mindset, with the confidence to challenge existing processes and suggest improvements.

• Experience experimenting with AI tools or vibe coding.
• Version control experience, such as Git.
• Knowledge of CDISC standards, including SDTM and ADaM.
• Familiarity with FDA and MHRA requirements, sponsor audits or regulatory inspections.
• SCDM certification.

• 40,000 to 48,000 salary, depending on experience.
• Permanent, full-time position.
• Hybrid working, with approximately 2 days per week in the office near Cambridge and the remainder from home.
• 26 days' annual leave plus bank holidays, including a Christmas shutdown allowance, with a holiday buy/sell scheme.
• Employer pension contributions of up to 6.5%.
• Life assurance at four times base salary.
• Private medical insurance through Bupa and a Medicash cashback scheme.
• Employee Assistance Programme.
• The opportunity to contribute to clinical research and technologies that support the development of new treatments.

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

If you're keen to join an exceptional global team where you can take ownership of clinical trial data delivery and help drive high-quality, efficient study outcomes, then please apply to this Senior Clinical Data Manager role below or call Chloe McCausland on (phone number removed) between 8:30am - 5:00pm.

For more info please contact Dani Adams on (phone number removed) / (phone number removed) / (url removed)

Locum Consultant in Oncology - UK-Wide Opportunities Medacs Healthcare

Job Title: Locum Consultant Clinical Oncologist - covering Urology

Location: Kent, UK

Rate: 110- 130ph, PAYE only

Contract Type: Locum

Details: Start ASAP for 3 months initially, with likely extension depending on substantive recruitment. Mon-Fri 9-5 (Friday afternoons off), full or part time considered. Job plan available on request. 4 clinics per week + admin, prescribing, planning and MDT.

Make a Real Difference in Oncology - On Your Terms

Are you a skilled Consultant in Oncology seeking flexibility, variety, and rewarding clinical experiences? At Medacs Healthcare, we're proud to support the NHS with expert consultants across the UK. We're currently recruiting for locum Consultant roles in Oncology with UK-wide opportunities tailored to your availability and preferences.

Why Work Locum with Medacs Healthcare?

• Priority Access to Locum Shifts - Get exclusive early access to locum roles across the UK.
• Shifts That Work for You - Flexible long-term or short-term assignments to match your lifestyle and career goals
• NHS-Approved Framework Agency - As a trusted Tier 1 supplier to over 150 NHS Trusts, we offer consistent, high-quality opportunities.
• Dedicated Recruitment Consultant - Receive one-to-one support from a specialist who understands your clinical area and career goals.
• Streamlined Registration & Fast Onboarding - Our expert compliance team helps you get fully registered and ready to work quickly and efficiently.
• Free Wellbeing Support - Benefit from free mental health and wellbeing support, including webinars by The Joyful Doctor (with CPD points)
• GMC Revalidation & Appraisal Support - We're a Designated Body and provide full support with your annual appraisals.
• Lucrative Referral Scheme - Earn generous bonuses for every successful referral you make.
• 24/7/365 Support - Our team is available around the clock - whenever you need us.

About the Role

As a locum Consultant in Oncology, you'll provide expert care and contribute to the delivery of high-quality services.

What We're Looking For

Essential:

• MBBS or equivalent medical degree
• Full GMC registration with a licence to practise
• A current Disclosure and Barring Service (DBS) check or PVG check - or a willingness to undergo one as part of the registration process
• UK Right to Work
• Relevant NHS experience

Desirable:

• CCT in Oncology

Locations Available

We're recruiting for locum roles across the UK, including:

• Greater London
• Midlands
• North West & North East England
• South East & South West England
• Scotland
• Wales

Let us know your preferred region and availability, and we'll match you with the right opportunity.

Apply Today

Take control of your oncology career with flexible locum opportunities through a trusted partner in healthcare staffing. Submit your CV below.

For more info please contact Dani Adams on (phone number removed) / (phone number removed) / (url removed)

For more info please contact Dani Adams on (phone number removed) / (phone number removed) / (url removed)

Locum Consultant or Specialist in Oncology - UK-Wide Opportunities Medacs Healthcare

Job Title: Locum Consultant or Specialist Clinical Oncologist - covering Gynae, Breast, Upper GI, Urology service (Breast and Gynae are priority)

Location: Lancashire, UK

Rate: 95- 135ph, PAYE only

Contract Type: Locum

Details: Start ASAP for 3 months initially. Full or part time considered. Some cross cover on another site may be required (25 min drive). We currently have significant pressures with Gynae , Breast, Upper GI, urology service. They would need experience within either of those (breast and Gynae are priority). Clinical Oncologist is very much preferable; to do Radiotherapy and Chemo.

Make a Real Difference in Oncology - On Your Terms

Are you a skilled Consultant in Oncology seeking flexibility, variety, and rewarding clinical experiences? At Medacs Healthcare, we're proud to support the NHS with expert consultants across the UK. We're currently recruiting for locum Consultant roles in Oncology with UK-wide opportunities tailored to your availability and preferences.

Why Work Locum with Medacs Healthcare?

• Priority Access to Locum Shifts - Get exclusive early access to locum roles across the UK.
• Shifts That Work for You - Flexible long-term or short-term assignments to match your lifestyle and career goals
• NHS-Approved Framework Agency - As a trusted Tier 1 supplier to over 150 NHS Trusts, we offer consistent, high-quality opportunities.
• Dedicated Recruitment Consultant - Receive one-to-one support from a specialist who understands your clinical area and career goals.
• Streamlined Registration & Fast Onboarding - Our expert compliance team helps you get fully registered and ready to work quickly and efficiently.
• Free Wellbeing Support - Benefit from free mental health and wellbeing support, including webinars by The Joyful Doctor (with CPD points)
• GMC Revalidation & Appraisal Support - We're a Designated Body and provide full support with your annual appraisals.
• Lucrative Referral Scheme - Earn generous bonuses for every successful referral you make.
• 24/7/365 Support - Our team is available around the clock - whenever you need us.

About the Role

As a locum Consultant in Oncology, you'll provide expert care and contribute to the delivery of high-quality services.

What We're Looking For

Essential:

• MBBS or equivalent medical degree
• Full GMC registration with a licence to practise
• A current Disclosure and Barring Service (DBS) check or PVG check - or a willingness to undergo one as part of the registration process
• UK Right to Work
• Relevant NHS experience

Desirable:

• CCT in Oncology

Locations Available

We're recruiting for locum roles across the UK, including:

• Greater London
• Midlands
• North West & North East England
• South East & South West England
• Scotland
• Wales

Let us know your preferred region and availability, and we'll match you with the right opportunity.

Apply Today

Take control of your oncology career with flexible locum opportunities through a trusted partner in healthcare staffing. Submit your CV below.

For more info please contact Dani Adams on (phone number removed) / (phone number removed) / (url removed)

Job Title: Senior Data Manager

Location: Welwyn gardens (2 or 3 days in a week)

Type: Contract (Outside IR 35)

We are looking for an experienced Senior Data Manager to oversee clinical trial data from setup to final database lock. You will ensure our study data is accurate, compliant, and ready for statistical analysis to help bring new treatments to market faster.

• Lead Study Data: Design trial databases/forms, clean data, and execute database locks.
• Ensure Quality: Resolve data discrepancies and manage external lab and tech vendors.
• Collaborate: Work closely with Biostatistics, Data Science, and Clinical Operations teams.

• Experience: Good years in Clinical Data Management.
• Education: Degree in Life Sciences, Computer Science, Statistics, or related field.
• Tech Skills: Hands-on experience with EDC systems and CDISC data standards.
• Bonus: Basic coding skills (SAS, R, or Python) and early-phase trial experience.

Interested? Apply now to join a team shaping the future of healthcare.

Randstad Technologies is acting as an Employment Business in relation to this vacancy.

Pharmaceutical Master Data Specialist West Lothian, Scotland

Opportunity:

Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards or TrackWise? Are you detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance? If yes then this is the role for you.

My client a global pharmaceutical manufacturing company are looking for a Master Data Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems.

Duties and responsibilities include:

• Generating and approving standard Item Masters, Item Branches, and Item Revisions within JD Edwards under established procedures.
• Generating and approving Location Masters and Location Master Revisions within JD Edwards under established procedures.
• Generating and approving Client Codes and Study Codes within Prisym under established procedures.
• Generating and approving Customer and Equipment Setup.
• Raising required Change Controls in Global TrackWise to support approved data revisions under established procedures.
• Performing assigned master data activities with attention to accuracy, completeness, and required turnaround times.
• Analysing and interpreting company and client documentation to determine correct data setup.
• Applying established data standards, guidelines, and SOPs in a GMP setting.

This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent on the candidate and business performance. The PAYE rate is between £13.58 - £15.60 per hour.

Skills:

To apply for the Pharmaceutical Master Data Specialist role you will have the following skills:

• Bsc in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent professional experience. APICS certification preferred.
• 0-3 years of relevant clinical supply, master data, project support, pharmaceutical, biotech, or equivalent business experience preferred.
• Detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance.
• Computer literate, with experience using spreadsheets, word processing programs, and business system tools.
• Willingness to travel preferred.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.

If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.

Pharmaceutical Master Data Specialist West Lothian, Scotland

Opportunity:

Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards or TrackWise? Are you detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance? If yes then this is the role for you.

My client a global pharmaceutical manufacturing company are looking for a Master Data Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems.

Duties and responsibilities include:

• Generating and approving standard Item Masters, Item Branches, and Item Revisions within JD Edwards under established procedures.
• Generating and approving Location Masters and Location Master Revisions within JD Edwards under established procedures.
• Generating and approving Client Codes and Study Codes within Prisym under established procedures.
• Generating and approving Customer and Equipment Setup.
• Raising required Change Controls in Global TrackWise to support approved data revisions under established procedures.
• Performing assigned master data activities with attention to accuracy, completeness, and required turnaround times.
• Analysing and interpreting company and client documentation to determine correct data setup.
• Applying established data standards, guidelines, and SOPs in a GMP setting.

This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent on the candidate and business performance. The PAYE rate is between £13.58 - £15.60 per hour.

Skills:

To apply for the Pharmaceutical Master Data Specialist role you will have the following skills:

• Bsc in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent professional experience. APICS certification preferred.
• 0-3 years of relevant clinical supply, master data, project support, pharmaceutical, biotech, or equivalent business experience preferred.
• Detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance.
• Computer literate, with experience using spreadsheets, word processing programs, and business system tools.
• Willingness to travel preferred.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.

If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.

Care Supervisor Field Based

Hillingdon & Uxbridge Plus Surrounding Areas

Full time: 40 hours per week

Working pattern: Scheduled over 5 days from 7, with some weekend work required as part of the rota.

Shifts: 7am 3pm and 2pm 10pm combination

Location: Hillingdon, Uxbridge & surrounding areas

Travel: Driver with own car required

Rate plus mileage: £29k per annum plus mileage

Right to work in the UK required as unable to offer sponsorship

Blue light discount card

Take the next step in your career.

Are you an experienced Care Worker ready to progress into supervision, or an existing Care Supervisor looking for a fresh opportunity?

Comfort Care Services is seeking a proactive and compassionate Field Care Supervisor to support the delivery of high-quality domiciliary care across Hillingdon and Uxbridge. This field-based role offers the opportunity to guide care teams, support service users and help maintain excellent standards of care and compliance.

What you ll be doing

• Supporting and supervising Care Workers in the community.
• Conducting spot checks, observations, supervisions and quality audits.
• Completing care assessments, reviews and reassessments.
• Monitoring care delivery and ensuring services are provided in line with individual support plans.
• Supporting medication audits, documentation and accurate record keeping.
• Helping to maintain staff rotas and effective handovers.
• Investigating incidents, escalating safeguarding concerns and resolving issues promptly.
• Building positive relationships with service users, families, care staff and professionals.
• Supporting hands-on care and service users needs when required.

What we re looking for

• Previous experience in domiciliary, community or other relevant care services.
• An experienced Care Worker ready to progress, or an existing Care Supervisor.
• QCF/NVQ Level 3 in Health & Social Care, or Level 2 with a commitment to enrol on and complete Level 3.
• Experience of supporting, supervising or managing staff.
• A full & valid driving licence and access to your own vehicle for business use.
• The right to work in the UK.
• Good knowledge of care standards, safeguarding, health and safety, and person-centred practice.
• Strong communication, organisation, administration and time-management skills.
• The flexibility to work across community locations and meet service needs.

Working pattern

• Full-time, 40 hours per week.
• 5 days over 7, including weekend working on a rota basis.
• A combination of 7am to 3pm and 2pm to 10pm shifts.
• Flexibility is required to meet the needs of the service.

What we offer

• £29,000 per annum, plus mileage for authorised business travel.
• 28 days annual leave, inclusive of bank holidays.
• Company pension scheme.
• Company mobile phone and laptop for business use.
• Mileage paid for business travel.
• Business car insurance costs paid. (up to £150.00)
• Ongoing training, professional development and career progression opportunities.
• Blue light discount card

Equality, inclusion and safeguarding

Comfort Care Services is committed to equality, diversity and inclusion, and welcomes applications from all backgrounds. We are also committed to safeguarding and promoting the welfare of vulnerable adults. Appointment will be subject to satisfactory references and an enhanced DBS check.

Important application requirements

Applicants must have the right to work in the UK. Sponsorship is not available for this vacancy. A full valid driving licence and access to a vehicle are required due to the field-based nature of the role.

Care Supervisor Supervisor Supervisor &SocialCare