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Laboratory Technician

hace 5 horas

Sant Feliu de Llobregat

ZeClinics is HIRING a Laboratory Technician! ZeClinics offers an exciting opportunity for a Laboratory Technician to be part of the team, whose mission is to provide an outsourcing solution for safety and efficacy screenings of novel chemical molecules using zebrafish. The ideal candidate would be responsible for performing experiments and support our Facility Manager in the daily organization of ZeClinics´s Laboratory. Duties of the Laboratory Technician will include: Perform the experimental tasks related to both scientific services offered by the company to third parties and research and development pipelines. Analyze the data deriving from experimental approaches. Ensure the correct use of defined laboratory equipment and maintain them up to date. Support the Project managers in redacting reports for clients (preparing the text and figures). Organize the data derived from the experiments and lab books to ensure full traceability of results. Support quality validation following GLP-like and GLP regulations and drafting SOPs. Support in regulatory studies if needed. Studies Holding a Bachelor’s or Master’s degree (and equivalent) in biotechnology, biology, biochemistry, biomedical laboratory science, or a related discipline will be necessary. Experience to value Proven experience with cellular biology, molecular biology, basic pharmacology, high throughput assays, and other biochemical, molecular, or cellular techniques will be mandatory. Experience with chemicals administration, microinjection, zebrafish biology, and husbandry will be positively evaluated. FELASA certification to perform scientific experiments with animals will be a plus. Additional skills Ability to work independently and interact with several collaborators Exceptional organizational skills with strict attention to detail Ability to manage multiple projects simultaneously under tight deadlines Languages Good command of Spanish is mandatory, knowledge of English both verbal and written, will be greatly appreciated. The Offer Duration: Indefinite contract Trial period: 3 months Estimated annual gross salary: Base remuneration: between 18,000 and 20,000 € gross per annum, commensurate with the candidate’s background. Performance-based incentives: approximately 6,000 to 7,000 €, contingent upon departmental results and 2025 business metrics. Flexibility is required to work on weekends during peak service periods, with the preference for having two days per week where weekly and weekend schedules can be interchanged. Starting date: As soon as possible Application Procedure All applications must include: - A presentation letter addressed to Anna Navarro (Project Manager), Christian Cortés Campos (Data Scientist) - A full CV including contact details - Two contacts for further references All applications must be sent to the HR DEPARTMENT by e-mail to hr@zeclinics.com

Laboratory Technician - ZeClinics

hace 8 horas

Sant Feliu de Llobregat

ZeClinics is HIRING a Laboratory Technician! ZeClinics offers an exciting opportunity for a Laboratory Technician to be part of the team, whose mission is to provide an outsourcing solution for safety and efficacy screenings of novel chemical molecules using zebrafish. The ideal candidate would be responsible for performing experiments and support our Facility Manager in the daily organization of ZeClinics´s Laboratory. Duties of the Laboratory Technician will include: • Perform the experimental tasks related to both scientific services offered by the company to third parties and research and development pipelines., • Analyze the data deriving from experimental approaches., • Ensure the correct use of defined laboratory equipment and maintain them up to date., • Support the Project managers in redacting reports for clients (preparing the text and figures)., • Organize the data derived from the experiments and lab books to ensure full traceability of results., • Support quality validation following GLP-like and GLP regulations and drafting SOPs., • Support in regulatory studies if needed. Studies Holding a Bachelor’s or Master’s degree (and equivalent) in biotechnology, biology, biochemistry, biomedical laboratory science, or a related discipline will be necessary. Experience to value • Proven experience with cellular biology, molecular biology, basic pharmacology, high throughput assays, and other biochemical, molecular, or cellular techniques will be mandatory., • Experience with chemicals administration, microinjection, zebrafish biology, and husbandry will be positively evaluated., • FELASA certification to perform scientific experiments with animals will be a plus. Additional skills • Ability to work independently and interact with several collaborators, • Exceptional organizational skills with strict attention to detail, • Ability to manage multiple projects simultaneously under tight deadlines Languages Good command of Spanish is mandatory, knowledge of English both verbal and written, will be greatly appreciated. The Offer • Duration: Indefinite contract, • Trial period: 3 months, • Estimated annual gross salary:, • Base remuneration: between 18,000 and 20,000 € gross per annum, commensurate with the candidate’s background., • Performance-based incentives: approximately 6,000 to 7,000 €, contingent upon departmental results and 2025 business metrics., • Flexibility is required to work on weekends during peak service periods, with the preference for having two days per week where weekly and weekend schedules can be interchanged., • Starting date: As soon as possible Application Procedure All applications must include: • A presentation letter addressed to Anna Navarro (Project Manager), Christian Cortés Campos (Data Scientist), • A full CV including contact details, • Two contacts for further references All applications must be sent to the HR DEPARTMENT by e-mail to

GLOBAL CLINICAL DEVELOPMENT PHYSICIAN - sant feliu de llobregat

hace 5 días

Sant Feliu de Llobregat

You may deputize on defined tasks, lead medical data review, and support protocol development, amendments, and scientific content. Support GCPL and Clinical Development Scientist in designing development plans and studies. Review scientific content of protocols, amendments, CSRs, ICF, CRF and relate

GLOBAL CLINICAL DEVELOPMENT PHYSICIAN

hace 5 días

Sant Feliu de Llobregat

Overview In this role you provide medical input and oversight for clinical development programs within Global Clinical Development, collaborating with cross-functional teams and GCPL/line managers. You may deputize on defined tasks, lead medical data review, and support protocol development, amendments, and scientific content. You will engage with Ethics Committees, investigators, and external KOLs to advance program delivery and publications, contributing to a patient-centric dermatology portfolio. Compensaciones / Beneficios • Top Employer Spain, • Top Employer Germany (first time), • people-centric culture, • opportunities for professional development Responsabilidades, • Support GCPL and Clinical Development Scientist in designing development plans and studies, • Back up GCPL responsibilities for defined tasks under supervision, • Contribute to study synopsis, protocol and amendments with GCPLs and CDS, • Review scientific content of protocols, amendments, CSRs, ICF, CRF and related documents (IB, briefing packages, ISE, ISS, publication), • Deputize GCPL as a member of the Global Project Team, • Provide medical support to Study Team for Ethics Committees and investigators, • Lead medical data review including eligibility and safety data, • Support protocol deviation review medically, • Partner with CDS and Clinical Operations to support study delivery (enrollment, eligibility, protocol violations, amendments), • Assist GCPL and CDS in data analysis, data review and publication content after study results, • Remain a core member of the Clinical Study Team, • Build relationships with external KOLs Requisitos principales, • Medical degree, • Dermatology specialty is a plus, • Prior experience in clinical studies (sub-investigator or industry/CRO), • Fluency in English (written and spoken), • Proficiency with MS Office, • Strong communication and presentation abilities, • Leadership and influence to drive consensus, • Analytical and problem-solving mindset, • MS Office, • Medical data review, • Clinical study documentation review