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Clinical Trial Manager
role at Solutia.Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.We are currently looking for a Clinical Trial Manager for a clinical-stage biotech company located in Barcelona.Purpose of the job:
Plan, budget, coordinate, and execute allocated clinical trials and assist with training and development of clinical monitoring tasks. Primary contact with CRO PM.Major accountabilities:
Oversee all clinical trial activities by project.Develop and track project plans with timelines and objectives, under the supervision of the Director of Clinical Operations.Contribute to trial-specific document development, site and CRO selection, and site initiation visits.Ensure data documentation and insurance requirements are met, and control the full execution of site contracts.Manage project deliverables, improve patient recruitment, ensure regulatory compliance, and meet objectives within budget and timelines.Report to the Clinical Development Director on quality, milestones, timelines, and budgets.Ensure the integrity of clinical data through review and oversight, detect and prevent misconduct, and implement corrective actions.Assist in planning key project milestones and develop project budgets to optimize costs and turnaround times.Manage internal and external partners, contracts, negotiations, and payments.Lead the in-house study team, coordinate activities of team members including CTO and CTAs, and lead CRAs and CTCs within the project team.Validate skills of outsourced trial teams, conduct training, and serve as on-site coach for CRAs.Manage CRO PM as the primary contact, review monitoring reports, and assist in audit reviews and CAPA plans.Lead IMP needs and supervise shipment activities, liaise with logistics vendors, and develop SOPs and study-specific procedures.Coordinate logistics activities for IMP availability and vendor contact.Requirements:
University degree in a scientific, medical, or paramedical field.Minimum five to ten years of experience in clinical research (Pharma or CRO).Experience in clinical development from Phase I to III.Excellent knowledge of clinical drug development process and global regulations (GCP, GPV, EMEA, FDA, ICH, local laws).Effective communication skills in English and Spanish.Ability to collaborate with project leaders, study teams, cross-functional teams, and external partners.Proficiency in email, Word, Excel, and project management skills.We offer a fixed contract, flexible entry hours, and a full-time employment in the research and project management sector within biotechnology, pharmaceutical manufacturing, and healthcare industries.
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