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Hays is collaborating with privately owned pharmaceutical company headquartered in Barcelona, with vertical integration covering the entire value chain from R&D to distribution founded in 1959. The company operates in more than 110 countries through 19 international subsidiaries. Its activities span the pharmaceutical, healthcare, fine chemicals, and nutrition sectors—key areas for contributing to improvements in people’s health and quality of life. We are looking for a Project Manager CRA to join their team and provide medical oversight across company clinical studies, helping to ensure participant safety, data quality, and medically sound decision-making throughout the conduct of clinical trials. To provide medical expertise on all medically relevant matters, including medical consultation, medical data review, and review of essential study documents. Also, give support the early identification of safety concerns across the clinical studies managed and overseen by company’s Clinical Development Department, ensuring a consistent and standardized approach to medical monitoring activities. As a key medical partner to internal teams and external providers, especially CROs, help ensure that medical monitoring activities are conducted in line with protocol, regulatory requirements, and ethical standards. In addition, contribute to fostering strong medical and scientific relationships with the broader scientific community. What would your duties be? • Provide medical consultation on study-related matters, including participant eligibility, protocol-related questions, efficacy and safety procedures, concomitant medication, adverse events, and SAE reporting., • Review SAE narratives and support the early identification of safety concerns across clinical studies., • Review and classify protocol deviations and assess exclusionary or alert laboratory values, as well as other relevant testing data., • Support the medical review of participant data listings, patient profiles, and medically coded terms to ensure consistency and medical appropriateness., • Provide guidance on investigational product administration issues when needed., • Lead medical discussions and teleconferences with internal study teams and external clinical service providers, including CROs., • Deliver therapeutic area and/or protocol training to relevant study team members., • Contribute to IRB/Ethics Committee and regulatory authority submissions when required., • Review and, when needed, co-author key study documents such as protocols, Medical Monitoring Plans, Safety Management Plans, Informed Consent Forms, and Clinical Study Reports., • Support patient enrolment activities when appropriate. Which are the requirements for this position? • Medical Degree with Registration Certificate., • At least 3 years of experience in Clinical Research., • GCP training., • Advanced level of English., • Experience reviewing clinical and safety data within clinical trials. This is consistent with the operational and medical-review focus described in the intake., • Strong medical judgment and the ability to interpret clinical data in a development context., • Good interpersonal skills and the ability to build effective relationships with both internal and external stakeholders., • Strong communication and presentation skills, with the ability to communicate clearly and concisely in writing., • Strategic thinking, attention to detail, and the ability to work effectively in crossfunctional team. What we offer? • Stable Project., • Flexible schedule., • Participate in international projects., • Flexible work., • Location: Barcelona but can be remote., • If we finally continue with your candidature in the recruitment process, at the end of it, we will request 2 previous references (it is part of the HAYS policy that any person who joins into our clients can provide contacts for making references process).

Hays is collaborating with privately owned pharmaceutical company headquartered in Barcelona, with vertical integration covering the entire value chain from R&D to distribution founded in 1959. The company operates in more than 110 countries through 19 international subsidiaries. Its activities span the pharmaceutical, healthcare, fine chemicals, and nutrition sectors—key areas for contributing to improvements in people’s health and quality of life. We are looking for a Project Manager CRA to join their team and provide medical oversight across company clinical studies, helping to ensure participant safety, data quality, and medically sound decision-making throughout the conduct of clinical trials. To provide medical expertise on all medically relevant matters, including medical consultation, medical data review, and review of essential study documents. Also, give support the early identification of safety concerns across the clinical studies managed and overseen by company’s Clinical Development Department, ensuring a consistent and standardized approach to medical monitoring activities. As a key medical partner to internal teams and external providers, especially CROs, help ensure that medical monitoring activities are conducted in line with protocol, regulatory requirements, and ethical standards. In addition, contribute to fostering strong medical and scientific relationships with the broader scientific community. What would your duties be? • Provide medical consultation on study-related matters, including participant eligibility, protocol-related questions, efficacy and safety procedures, concomitant medication, adverse events, and SAE reporting., • Review SAE narratives and support the early identification of safety concerns across clinical studies., • Review and classify protocol deviations and assess exclusionary or alert laboratory values, as well as other relevant testing data., • Support the medical review of participant data listings, patient profiles, and medically coded terms to ensure consistency and medical appropriateness., • Provide guidance on investigational product administration issues when needed., • Lead medical discussions and teleconferences with internal study teams and external clinical service providers, including CROs., • Deliver therapeutic area and/or protocol training to relevant study team members., • Contribute to IRB/Ethics Committee and regulatory authority submissions when required., • Review and, when needed, co-author key study documents such as protocols, Medical Monitoring Plans, Safety Management Plans, Informed Consent Forms, and Clinical Study Reports., • Support patient enrolment activities when appropriate. Which are the requirements for this position? • Medical Degree with Registration Certificate., • At least 3 years of experience in Clinical Research., • GCP training., • Advanced level of English., • Experience reviewing clinical and safety data within clinical trials. This is consistent with the operational and medical-review focus described in the intake., • Strong medical judgment and the ability to interpret clinical data in a development context., • Good interpersonal skills and the ability to build effective relationships with both internal and external stakeholders., • Strong communication and presentation skills, with the ability to communicate clearly and concisely in writing., • Strategic thinking, attention to detail, and the ability to work effectively in crossfunctional team. What we offer? • Stable Project., • Flexible schedule., • Participate in international projects., • Flexible work., • Location: Barcelona but can be remote., • If we finally continue with your candidature in the recruitment process, at the end of it, we will request 2 previous references (it is part of the HAYS policy that any person who joins into our clients can provide contacts for making references process).

About ANZEN Engineering: ANZEN Engineering is a leading engineering company specialized in supporting the development and certification of Safety- Critical & Mission-Critical systems. We collaborate in the most relevant aerospace & defence programs across more than ten countries, delivering value on a global scale with an onsite presence in the USA, Europe, and the Middle East. We are seeking an Electrical Engineer to join our engineering team in Madrid, Spain. Main responsibilities: • Design and develop EWIS including wire harnesses, cable assemblies, and connector systems compliant with DO-160, SAE AS50881, MIL-DTL-38999, and FAA AC 21-99(0)., • Perform wire gauge calculations, voltage drop analysis, and current capacity assessments. Select materials, connectors, terminals, and protective components based on environmental and performance requirements., • Develop grounding/bonding schemes for electrical safety and EMC compliance., • Create harness assembly drawings, wire lists, installation procedures, tooling requirements, and manufacturing documentation., • Coordinate wire routing through bulkheads, fairings, and structural members, ensuring proper support, strain relief, bend radius, clearances, and protection from chafing, vibration, and environmental hazards., • Support prototype builds and production installations with hands-on guidance; verify proper EWIS component installation., • Develop and execute test plans for continuity, insulation resistance, and functional testing; perform acceptance testing, quality inspections, and fault isolation., • Create and maintain technical documentation including wiring diagrams, ICDs, installation manuals, work instructions, QC procedures, and parts lists., • Coordinate with manufacturing, quality teams, and suppliers to optimize harness producibility, reduce assembly time, and support procurement. Qualifications: • Bachelor's in Electrical or Aerospace Engineering (Master's a plus), • 3–5 years in EWIS design, wire harness development, or aerospace electrical systems, • Hands-on experience with assembly, installation, and testing preferred., • Strong understanding of electrical wiring principles, wire sizing, circuit protection, and EMC/EMI requirements., • Proficiency with electrical CAD tools (e.g. Capital Harness, CATIA Electrical Workbench), familiarity with connector systems, termination techniques, and testing equipment (multimeters, continuity/hipot testers)., • Knowledge of wire protection methods, composite aircraft EWIS challenges, and aerospace standards (SAE AS50881, FAA AC 21-99(0), DO-160, AS9100/ISO 9001), including lightning and HIRF protection., • Analytical, detail-oriented, and effective in cross-functional teams; able to work independently across office and production floor environments., • English proficiency required, German a plus. What we offer • Participation in leading international programs., • Excellent salary conditions, commensurate with experience., • 40-hour work week., • Permanent contract., • Highly motivating work environment., • Being part of the company’s growth and expansion., • Significant opportunities for professional growth due to the company’s rapid expansion.

About ANZEN Engineering: ANZEN Engineering is a leading engineering company specialized in supporting the development and certification of Safety- Critical & Mission-Critical systems. We collaborate in the most relevant aerospace & defence programs across more than ten countries, delivering value on a global scale with an onsite presence in the USA, Europe, and the Middle East. We are seeking an Electrical Engineer to join our engineering team in Madrid, Spain. Main responsibilities: • Design and develop EWIS including wire harnesses, cable assemblies, and connector systems compliant with DO-160, SAE AS50881, MIL-DTL-38999, and FAA AC 21-99(0)., • Perform wire gauge calculations, voltage drop analysis, and current capacity assessments. Select materials, connectors, terminals, and protective components based on environmental and performance requirements., • Develop grounding/bonding schemes for electrical safety and EMC compliance., • Create harness assembly drawings, wire lists, installation procedures, tooling requirements, and manufacturing documentation., • Coordinate wire routing through bulkheads, fairings, and structural members, ensuring proper support, strain relief, bend radius, clearances, and protection from chafing, vibration, and environmental hazards., • Support prototype builds and production installations with hands-on guidance; verify proper EWIS component installation., • Develop and execute test plans for continuity, insulation resistance, and functional testing; perform acceptance testing, quality inspections, and fault isolation., • Create and maintain technical documentation including wiring diagrams, ICDs, installation manuals, work instructions, QC procedures, and parts lists., • Coordinate with manufacturing, quality teams, and suppliers to optimize harness producibility, reduce assembly time, and support procurement. Qualifications: • Bachelor's in Electrical or Aerospace Engineering (Master's a plus), • 3–5 years in EWIS design, wire harness development, or aerospace electrical systems, • Hands-on experience with assembly, installation, and testing preferred., • Strong understanding of electrical wiring principles, wire sizing, circuit protection, and EMC/EMI requirements., • Proficiency with electrical CAD tools (e.g. Capital Harness, CATIA Electrical Workbench), familiarity with connector systems, termination techniques, and testing equipment (multimeters, continuity/hipot testers)., • Knowledge of wire protection methods, composite aircraft EWIS challenges, and aerospace standards (SAE AS50881, FAA AC 21-99(0), DO-160, AS9100/ISO 9001), including lightning and HIRF protection., • Analytical, detail-oriented, and effective in cross-functional teams; able to work independently across office and production floor environments., • English proficiency required, German a plus. What we offer • Participation in leading international programs., • Excellent salary conditions, commensurate with experience., • 40-hour work week., • Permanent contract., • Highly motivating work environment., • Being part of the company’s growth and expansion., • Significant opportunities for professional growth due to the company’s rapid expansion.

About ANZEN Engineering: ANZEN Engineering is a leading engineering company specialized in supporting the development and certification of Safety- Critical & Mission-Critical systems. We collaborate in the most relevant aerospace & defence programs across more than ten countries, delivering value on a global scale with an onsite presence in the USA, Europe, and the Middle East. We are seeking an Electrical Engineer to join our engineering team in Madrid, Spain. Main responsibilities: • Design and develop EWIS including wire harnesses, cable assemblies, and connector systems compliant with DO-160, SAE AS50881, MIL-DTL-38999, and FAA AC 21-99(0)., • Perform wire gauge calculations, voltage drop analysis, and current capacity assessments. Select materials, connectors, terminals, and protective components based on environmental and performance requirements., • Develop grounding/bonding schemes for electrical safety and EMC compliance., • Create harness assembly drawings, wire lists, installation procedures, tooling requirements, and manufacturing documentation., • Coordinate wire routing through bulkheads, fairings, and structural members, ensuring proper support, strain relief, bend radius, clearances, and protection from chafing, vibration, and environmental hazards., • Support prototype builds and production installations with hands-on guidance; verify proper EWIS component installation., • Develop and execute test plans for continuity, insulation resistance, and functional testing; perform acceptance testing, quality inspections, and fault isolation., • Create and maintain technical documentation including wiring diagrams, ICDs, installation manuals, work instructions, QC procedures, and parts lists., • Coordinate with manufacturing, quality teams, and suppliers to optimize harness producibility, reduce assembly time, and support procurement. Qualifications: • Bachelor's in Electrical or Aerospace Engineering (Master's a plus), • 3–5 years in EWIS design, wire harness development, or aerospace electrical systems, • Hands-on experience with assembly, installation, and testing preferred., • Strong understanding of electrical wiring principles, wire sizing, circuit protection, and EMC/EMI requirements., • Proficiency with electrical CAD tools (e.g. Capital Harness, CATIA Electrical Workbench), familiarity with connector systems, termination techniques, and testing equipment (multimeters, continuity/hipot testers)., • Knowledge of wire protection methods, composite aircraft EWIS challenges, and aerospace standards (SAE AS50881, FAA AC 21-99(0), DO-160, AS9100/ISO 9001), including lightning and HIRF protection., • Analytical, detail-oriented, and effective in cross-functional teams; able to work independently across office and production floor environments., • English proficiency required, German a plus. What we offer • Participation in leading international programs., • Excellent salary conditions, commensurate with experience., • 40-hour work week., • Permanent contract., • Highly motivating work environment., • Being part of the company’s growth and expansion., • Significant opportunities for professional growth due to the company’s rapid expansion.

Hays is collaborating with privately owned pharmaceutical company headquartered in Barcelona, with vertical integration covering the entire value chain from R&D to distribution founded in 1959. The company operates in more than 110 countries through 19 international subsidiaries. Its activities span the pharmaceutical, healthcare, fine chemicals, and nutrition sectors—key areas for contributing to improvements in people’s health and quality of life. We are looking for a Project Manager CRA to join their team and provide medical oversight across company clinical studies, helping to ensure participant safety, data quality, and medically sound decision-making throughout the conduct of clinical trials. To provide medical expertise on all medically relevant matters, including medical consultation, medical data review, and review of essential study documents. Also, give support the early identification of safety concerns across the clinical studies managed and overseen by company’s Clinical Development Department, ensuring a consistent and standardized approach to medical monitoring activities. As a key medical partner to internal teams and external providers, especially CROs, help ensure that medical monitoring activities are conducted in line with protocol, regulatory requirements, and ethical standards. In addition, contribute to fostering strong medical and scientific relationships with the broader scientific community. What would your duties be? • Provide medical consultation on study-related matters, including participant eligibility, protocol-related questions, efficacy and safety procedures, concomitant medication, adverse events, and SAE reporting., • Review SAE narratives and support the early identification of safety concerns across clinical studies., • Review and classify protocol deviations and assess exclusionary or alert laboratory values, as well as other relevant testing data., • Support the medical review of participant data listings, patient profiles, and medically coded terms to ensure consistency and medical appropriateness., • Provide guidance on investigational product administration issues when needed., • Lead medical discussions and teleconferences with internal study teams and external clinical service providers, including CROs., • Deliver therapeutic area and/or protocol training to relevant study team members., • Contribute to IRB/Ethics Committee and regulatory authority submissions when required., • Review and, when needed, co-author key study documents such as protocols, Medical Monitoring Plans, Safety Management Plans, Informed Consent Forms, and Clinical Study Reports., • Support patient enrolment activities when appropriate. Which are the requirements for this position? • Medical Degree with Registration Certificate., • At least 3 years of experience in Clinical Research., • GCP training., • Advanced level of English., • Experience reviewing clinical and safety data within clinical trials. This is consistent with the operational and medical-review focus described in the intake., • Strong medical judgment and the ability to interpret clinical data in a development context., • Good interpersonal skills and the ability to build effective relationships with both internal and external stakeholders., • Strong communication and presentation skills, with the ability to communicate clearly and concisely in writing., • Strategic thinking, attention to detail, and the ability to work effectively in crossfunctional team. What we offer? • Stable Project., • Flexible schedule., • Participate in international projects., • Flexible work., • Location: Barcelona but can be remote., • If we finally continue with your candidature in the recruitment process, at the end of it, we will request 2 previous references (it is part of the HAYS policy that any person who joins into our clients can provide contacts for making references process).

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