REQUIREMENTS Cláusulas de Ejemplo

REQUIREMENTS. The Supplier must purchase and maintain at its own costs and expense, a commercial general liability insurance from a financially sound and reputable insurance company in order to cover its liability toward the Company, our Customer or any third party resulting from defective Contractual Products and/or Contractual Services, product supplied as well as service provided. This insurance must include coverage for bodily injury, property damage, consequential loss as well as pure financial loss. Requisitos. El Proveedor deberá comprar y mantener bajo su propio costo y gasto un seguro comercial general de responsabilidad civil de una aseguradora solvente y de prestigio con la finalidad de cubrir su responsabilidad hacia la Compañía, nuestro Cliente o cualquier tercero que resulte de los Productos del Contrato y/o Servicios del Contrato defectuosos, productos suministrados, así como el servicio proporcionado. Este seguro deberá incluir una cobertura por lesiones corporales, daños a la propiedad, daños indirectos, así como daños puramente patrimoniales.

REQUIREMENTS a) TITLE • Graduated in Nursing.

REQUIREMENTS a) DEGREE b) OTHER REQUIREMENTS • High communication skills. • Ability to work independently and as part of a team. • Linguistic competence: ability to understand and communicate in English.

REQUIREMENTS a) EDUCATION. Essential Requirements • Degree in Health Sciences with a Master's degree.

REQUIREMENTS a) QUALIFICATIONS The candidate must hold the following qualifications: • Higher Vocational Training (FPII) in Clinical Diagnostic Laboratory • Higher Vocational Training (FPII) in Administration and Finance b) EXPERIENCE • At least 6 years of experience in a similar role‌ • Experience in clinical and basic research on Eosinophilic Esophagitis • Experience as a Clinical Trial Coordinator • Handling of biological samples • Experience and proficiency with HCIS‌ • Dangerous goods transport certificate c) OTHER • Experience in programming, managing, and exploiting databases • Proficiency with software tools and programs: RedCap, iMedidata, Oracle, and statistical analysis packages (SPSS, Stata, R) • Experience presenting documentation to the CEIC‌ • Relationship with AEDESEO professionals • Development of standardized CVs in FECYT • Participation in and organization of Eosinophilic Esophagitis conferences and congresses • Publications in the field of Eosinophilic Esophagitis‌ • Training in Good Clinical Practice • Excellent patient care with problem-solving skills • Professional with initiative, coordination, and management skills • Intermediate English language proficiency

REQUIREMENTS a) EDUCATION • Bachelor's degree in Biotechnology and a Master's in Microbiology. b) EXPERIENCE • At least 12 months of prior experience in a translational immunology research laboratory.‌ • Research experience with cell cultures of human mast cell lines and primary mouse bone marrow lines. • Scientific publications in indexed journals. • Experience with protocols for isolating sensory neurons from mice. • Experience in mast cell desensitization protocols. • Proficiency with flow cytometry and the FlowJo analysis software.‌ • Experience with enzymatic assays. c) OTHER • Prior experience in an immunology research laboratory. • Knowledge of handling patient biological samples. • Proficiency with statistical analysis and data processing software. • Certification in animal experimentation (functions A, B, and C). • C1 English language proficiency (Advanced Certificate or equivalent).

REQUIREMENTS a) EDUCATION • Bachelor's degree in a health sciences field. b) MINIMUM EXPERIENCE OF 6 MONTHS • Previous experience as a Data Entry in Dermatology. Participation in clinical trials for psoriasis, atopic dermatitis, hidradenitis suppurativa, and chronic urticaria. • Previous experience in Pharmacovigilance. • Previous experience in clinical research projects on dermatological diseases c) OTHER SKILLS • Proficiency in electronic data capture tools and IRT systems: RedCap, iMedidata, Oracle, Cenduit, Suvoda, Almac, Endpoint, etc. • Training in Good Clinical Practice Guidelines with an official valid certificate. • Training in handling biological samples with a valid official certificate (IATA). • English language proficiency at a C1 level.

REQUIREMENTS. The documentation must be available to the Biomedical Research Foundation. a) QUALIFICATION. Essential Requirements • Bachelor's degree in Law or a degree with a master's degree, specializing in Administrative Law, Commercial Law, or related areas. b) EXPERIENCE • Minimum of 2 years of experience in a similar position, preferably in the biomedical, pharmaceutical, or research sector. c) ADDITIONAL REQUIREMENTS • Additional training in public procurement, intellectual property, or compliance is a plus. • Experience in managing public and private contracts, and handling donations and agreements with the pharmaceutical industry. • Excellent contract negotiation and drafting skills. • Ability to interpret and apply complex legal regulations. • Ability to work autonomously and make informed decisions. • Excellent communication skills and ability to work in a team. • Proficiency in Spanish and English (advanced level). • Experience in Technology Law and Intellectual Property: Demonstrated experience in managing legal issues related to technology, including intellectual property, technology contracts, and software licenses. • Knowledge of Data Protection and Privacy: Familiarity with relevant data protection and privacy laws, such as GDPR in Europe and other local and international regulations.

REQUIREMENTS. Documentation must be available to the Fundación para la Investigación Biomédica. a) QUALIFICATIONS. Essential requirements • Higher education in a biosanitary area. • Master's degree in Monitoring or Coordination of Clinical Trials. b) EXPERIENCE • Experience in clinical trial monitoring. • Experience providing administrative and documentary support in managing contracts with centers as well as liaising with Ethics Committees and the Spanish Agency of Medicines and Medical Devices (AEMPS). • Knowledge of Good Clinical Practice guidelines. c) OTHER REQUIREMENTS • Experience in clinical research within the framework of biomedical projects. • Previous experience working with the Spanish Clinical Research Network (SCReN) will be valued. • Proficiency in Office, database management, and statistical analysis packages. • Medium level of spoken and written English.

REQUIREMENTS a) EDUCATION. Essential Requirements • Degree in Nursing with a Master's degree.