Key Responsibilities Database programming and data acquisition: Design, write and maintain database programs and scripts in CQL, R and Python. Use them to acquire, transform, reconcile and quality-check clinical and external vendor data (central labs, sequencing, biomarkers, imaging, eCOA/ePRO), and integrate it into GSK systems. AI/ML and automation: Identify, evaluate and pilot AI/ML and automation, working with Data Management, Clinical teams. Examples are ML-based anomaly detection beyond rule-based edit checks, AI-assisted Data mapping, NLP/OCR for unstructured data, and predictive risk insight. Hold AI/ML programming awareness (Python/R ML libraries, model validation, bias and limitations) and be a credible partner to technical teams. Delivery and vendor oversight: Deliver multiple clinical studies across all data acquisition activities, including timelines, oversight and governance of external vendors, and driving team members to meet milestones. Study team advisory: Advise Study Core Team members on DM operational and technical requirements. Provide input to study design, the protocol and study planning, and coordinate review and approval of specifications and vendor deliverables (including translations). Issue resolution and reporting: Mediate and solve data acquisition issues, escalating as needed. Report status and risks to the Study Data Manager, ensure quality control of deliverables, and run after-action reviews to share learnings. Data standards and transformation: Apply CDISC/SDTM standards and develop programmatic transformations of clinical laboratory and vendor data. Maintain data flow and database architecture integrity (Oracle, Unix). Compliant and responsible AI/ML use: Ensure programmed and AI/ML-enabled solutions are validated, auditable and explainable, and comply with GxP, ICH-GCP, data privacy and GSK AI governance. Keep human review in place for AI-generated outputs. SME and capability building: Act as Subject Matter Expert for process improvement, new processes, training, quality assessments, audits and inspections. Mentor junior team members in programming and emerging technologies, and line-manage a small team as required. Outsourced studies and compliance: For e2e DM FSP or FSO studies, support the Study Data Manager and Oversight Data Manager on ePRO, eCOA and other vendor data matters. Adhere to SOPs, corporate policies, regulatory requirements and industry best practice. Education Bachelor's degree or equivalent in Engineering, Life Sciences, Computer Science, Mathematics, Physics or equivalent. Needed to understand complex processes, study designs and systems in the pharmaceutical industry. Experience 8+ years of experience in data acquisition or related roles in clinical research or information systems, and/or relevant scientific experience. Demonstrated ability to deliver clinical data management tasks to time, quality and DM process compliance, with sufficient autonomy in highly complex study set-up with multiple stakeholders. Ability to act as SME, mentor and technical advisor on complex concerns. Preferred Hands-on experience applying analytics, automation or AI/ML in clinical data management or a related data-intensive environment. Hard Skills Experienced in Data Management in the pharmaceutical industry; good understanding of regulations including ICH-GCP. Experience with CDISC standards, including SDTM. Database programming (Must): proficiency in SQL with working knowledge of R and Python for data extraction, transformation, reconciliation, validation and reporting. Familiarity with other languages (e.g. SAS, C#) is an advantage. Experience working in database systems and environments; understanding of data flow and database architecture concepts. AI/ML awareness (Must): working understanding of core AI/ML concepts (supervised/unsupervised learning, model training and validation, NLP, generative AI/LLMs), their limitations (bias, hallucination, data quality) and appropriate use cases in clinical data acquisition. Familiarity with Python/R ML libraries is an advantage. Expertise in eDC solutions (InForm, Rave, Veeva CDMS/Vault) and ePRO/eCOA solutions. Experience developing programmatic transformations of clinical laboratory data; knowledge of medical terminology related to biospecimen collection and assessment. Knowledge of data types such as central labs, RNA/DNA sequencing, flow cytometry, complex biomarkers, eCOA, microscopy, immunohistochemistry, ocular assessments and imaging. Ability to explain complex technical principles to non-technical staff; experience managing business remotely in a matrix network. Soft Skills Excellent communication skills in a matrix environment; presentation and training skills; fluent English (written and spoken). Good analytical, problem-solving and project delivery skills; results oriented and customer focused. Strong ability to mentor teams; team spirit and ability to facilitate interfaces across an extended network. Good time management; ability to anticipate change and implement it flexibly; proactive and stress resistant. Able to manage complex planning conflicts in multi-disciplinary meetings and propose pragmatic solutions. Innovative, process-minded and open to new technologies; quick learner with curiosity about emerging tools such as AI/ML. Skills Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Inclusion at GSK: As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss your needs. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine. We are a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Find out more on our career site.

Manager, Data Acquisition.

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