A dynamic biopharmaceutical company is seeking a Clinical Trial Associate (CTA) to support the Clinical Operations team across all aspects of study management. This role focuses on TMF oversight, clinical documentation, and day-to-day project coordination within a fast-paced, outsourced environment.The organization is dedicated to developing innovative therapies for patients with rare diseases. Their mission is to deliver impactful treatments by running high-quality, patient-focused clinical trials with efficiency and precision.Key ResponsibilitiesTMF & Documentation: Manage eTMF setup, quality control, audit readiness, and archiving; support Sponsor oversight and documentation compliance.Clinical Support: Track study milestones, organize training records, assist with vendor coordination, meeting scheduling, and material distribution.Project Coordination: Provide administrative support to the Clinical team, take meeting minutes, and help ensure alignment with ICH-GCP and SOPs.Key RequirementsExperience: Previous experience in pharma/biotech; hands-on expertise with eTMF systems is essential.Skills: Strong organizational, multitasking, and communication skills; high attention to detail and proficiency in Microsoft Office and SharePoint.Attributes: Self-starter, adaptable, reliable, and able to work effectively in a small, collaborative team environment.

SciPro are partnered with a growing biopharmaceutical company is seeking a Clinical Trial Manager to support the planning and execution of global clinical trials in collaboration with the Director of Clinical Operations. This role is critical in ensuring clinical programs are delivered on time, within budget, and in line with regulatory and quality standards for a best-in-class therapy.The organization is focused on advancing transformative therapies for patients with rare macrophage-mediated diseases. Their mission is to improve patient outcomes by delivering scientifically driven, high-quality clinical programs with speed and precision.Key ResponsibilitiesTrial Management: Lead the development of trial plans, budgets, and timelines; oversee execution and ensure alignment with clinical and regulatory goals.Stakeholder Engagement: Act as the main point of contact for cross-functional teams, investigators, and vendors; drive collaboration and resolve project issues.Compliance & Quality: Maintain GCP and regulatory adherence across all trial activities; manage audits, documentation, and implement risk mitigation strategies.Key RequirementsExperience: Proven background in clinical project management, ideally within biotech or a start-up setting; successful delivery of complex trials from start to finish.Skills: Strong leadership, communication, and project management skills; proficient in tools like Microsoft Project, Excel, and EDC systems.Certifications: PMP or CCRA certification is desirable; ability to mentor and operate within a dynamic, high-performance team environment.