Clinical data jobs in Edinburgh - Page 2Crear alertas

The successful candidate will be responsible for assisting patients with completing questionnaires and managing the submission of surgical data to ensure compliance with reporting deadlines.

A leading biostatistics firm is seeking an experienced professional to provide technical leadership in SAS programs for analyzing clinical trial data.

Strong knowledge of clinical data management processes and regulatory requirements (GCP). Provide subject matter expertise in data management processes and systems. This role serves as the primary point of contact for data management on assigned projects, ensuring high-quality deliverables are compl

A clinical research company in the UK is looking for a Data Analyst I to provide backend support for the Financial Team. This role involves processing data and reconciling payments for clinical research studies.

The successful candidate will ensure the accuracy of clinical trial data, collaborate with internal teams, and maintain high-quality databases. A pharmaceutical development company is seeking a Data Manager III in Edinburgh, Scotland.

The post holder will be responsible for the validation and submission of patient outcomes data onto the Trusts clinical effectiveness platform 'Amplitude' and mandatory data to the National Joint Registry (NJR) and Patient Reported Outcomes Measures (PROMS) on every eligible patient who undergoes su

A leading clinical data management company in the United Kingdom is seeking a Senior Clinical Data Management Project Lead to oversee data management services for clinical projects. This full-time contract position focuses on quality assurance, project management, client relations, and team leadersh

A leading global healthcare consulting firm in the United Kingdom is seeking an experienced Senior Data Management Programmer. The role involves leading programming tasks for clinical trials while owning specifications and validation processes. Candidates should have 5+ years of SAS programming expe

A leading global university in the UK seeks a Senior Data Manager for the Birmingham Clinical Trials Unit. The role involves managing clinical research data, ensuring accuracy, and providing support to multi-disciplinary research groups. Candidates should have a degree in a biomedical field and expe

A leading medical laboratory hub in the UK is seeking a candidate for a role focused on medical coding and administration of clinical data. The responsibilities include ensuring data security, summarizing medical information, managing risk in practices, and mentoring junior staff.

A leading AI technology firm is seeking a Principal Clinical Scientist to drive expertise in clinical trial design and ensure regulatory standards in data interpretation. The ideal candidate will possess senior-level experience in clinical trials, a strong background in research methodology, and the

A healthcare consulting firm is seeking a Lead CDM responsible for the end-to-end delivery of data management services for disease registry studies. This remote position requires significant experience, specifically over 7 years in data management and at least 4 years in budget management and client

Have knowledge of database structure and data management techniques,. Collaborate with the project team on the overall data management strategy for the program or project to ensure overall quality and efficiency. Lead the development of CRF specifications, validate them, and conduct editorial review

This role focuses on providing technical support for clinical documentation projects, developing training programs, and optimizing processes. Ideal candidates will have strong technical expertise and a background in clinical documentation.

The ideal candidate will hold a relevant degree and have experience in clinical research and a strong understanding of eCOA.

A leading global healthcare consulting firm is seeking a Senior Data Manager to oversee data management for clinical trials.

Support the delivery of clinical research in accordance with Good Clinical Practice (GCP), the Declaration of Helsinki, applicable legislation (including, but not limited to, the Medicines for Human Use Clinical Trials Regulations, Data Protection Act 2018, Human Tissue Act), the Research Governance

Data Management plan (DMP), Data Validation Plan (DVP), Data Entry Guideline, Database Specification Document (DBSD), Database Report (DBR)) in the DM TMF. Provide validated data exports from the EDC system or the clinical database to authorized recipients (e. Perform clinical database development,