At a Glance
- Tasks: Lead the setup and development of electronic data capture solutions for clinical studies.
- Company: Join a pioneering company in clinical research with a focus on innovation.
- Benefits: Attractive salary, health benefits, flexible working options, and growth opportunities.
- Other info: Collaborative environment with a focus on continuous improvement and learning.
- Why this job: Make a difference in healthcare by managing data for impactful clinical trials.
- Qualifications: Experience in data management and strong communication skills required.
The predicted salary is between 45000 - 55000 £ per year.
Key Responsibilities
- Perform the study set-up activities and the technical development of Electronic Data capture (e DC) solutions and associated tools for one or more clinical study(ies).
- Assist with the technical & vendor oversight of multiple data types for one or more clinical study(ies).
- Support the delivery of one or more Clinical studies depending upon the phase, complexity, and similarity with support of junior data acquisitions staffs as required.
• For studies, key responsibilities include
- Provides input to study design, the clinical protocol, study planning and review of study documents as appropriate.
- Coordinates review, revision, and approval of study specification documents (including operational requirements & specifications) and/or key vendor deliverables (including translations).
- Understands, mediates and solves issues related to Data acquisition.
Develops the study e DC application and associated documents including forms, data validation checks & data extraction and ensures delivery with quality and on time.
- Provides reports, status updates, feedback, and raises risks and advice to Study Data Manager about study set-up and/or vendor related activities.
- Ensures quality control of deliverables.
- Provide inputs to process improvements, new processes, training, quality assessments, audits and inspections related to the Data Acquisition.
- Responsible for performing after-action reviews (success or failure) to share learnings and propose improvements for the future.
- Extensive working knowledge of Gx P, ICH requirements, internal processes and external regulations that govern drug development (where applicable).
Skills
- Agile Thinking
- Clinical Data Management
- Clinical Development
- Clinical Information Systems
- Clinical Trial Designs
- Communication
- Creativity
- Data Analysis
- Data Management
- Data Standards
- Data Validation
- Influencing Without Authority
- Risk Management
- Stakeholder Management
- Teamwork
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Senior Analyst, Data Acquisition employer: Gsk
GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.
