SciPro are partnering with a growing independent pharmaceutical company who are seeking a Clinical Programmer to support the transition from paper-based data collection to electronic systems across their clinical studies.This role will take ownership of building and maintaining EDC databases, ensuring high-quality, compliant clinical data, and supporting the implementation and day-to-day management of key clinical systems. Key Responsibilities Build and maintain EDC study databases and eCRFs, including edit checks, UAT, and database go-liveSupport data cleaning, validation, QC, and reportingManage data transfers with external vendorsSupport implementation and maintenance of EDC, eTMF, and CTMSEnsure compliance with GCP, GDPR, and data standards (e.g. CDISC/SDTM)Act as a key database contact for clinical and project teams Experience Required Experience building EDC databases and programming edit checksBackground working with clinical study dataExperience with data/programming tools (e.g. SAS, SPSS, or similar)Strong attention to detail and collaborative mindset If you’d like to play a hands-on role in shaping clinical data systems within a growing organisation, we’d love to hear from you. 

 Pharmacovigilance Physician - Oncology REMOTE Competitive Compensation Package Based on Experience SciPro Global is exclusively partnered with an Oncology biotech with promising science that is growing their Safety group as their pipeline progresses. This is the second hire for this group, reporting directly into the Vice President of Safety, and individual who is a calm leader with strong abilitiy to train their team.  Responsibilities include (but not limited to): Safety analysis of both clinical trials & post marketed products.Leading clinical safety aggregate reports such PADERs.Leading risk mitigation and risk minimization measures for global studies, specifically working with RMPs.Responding to health authority queries regarding safety & risk sections of regulatory documents.Perform signal management & lead signal strategy measures.Safety surveillance of all assigned products.Cross functionally act as Safety SME for assigned products & liaise with other Clinical counterparts across the organization.Communicate safety updates with external & internal stakeholders.Provide safety input for clinical study design activities.Identify ways of improvement for team & safety group.  Requirements include (but not limited to): Medical Director or Foreign Equivalent.Minimum 3 years of Pharmacovigilance & Safety experience at a Biotech or Pharma.Oncology Experience required.Management experience.Solution Oriented mindset & motivated!  Are you looking to join a brand name company to grow your career? Apply now to begin the process!