Last updated: 2025-05-22

21 Biopharmaceutical Leadership jobs in Remote - Kingdom of Spain.

Hiring now: Site Care Partnersr Cra F @ Parexel, Clinical Research Associa @ Iqvia, Srprincipal Clinical Data @ Precision , Srprincipal Clinical Data @ Precision , Sr Dir Global Program Tea @ Astrazenec, Team Mgr Veeva Rim Profes @ Veeva Syst, Sr Feasibility Associatef @ Precisionm, Sr Clinical Data Mgrprinc @ Pfm.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical research (6) programming (5) CDISC standards (5) Clinical Trials (4) EDC vendor (4) Data Management (4) scripting (4) data management (4) drug development (4) regulatory submissions (3)

šŸ“ Locations

Kingdom of Spain (21)

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner

Iqvia

Skills & Focus: Clinical Research, site selection, monitoring, Good Clinical Practice, International Conference on Harmonization, regulatory submissions, data query resolutions, effective working relationships, problem-solving skills, therapeutic knowledge
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Resources that promote your career growth, flexible work schedules, excellent working environment

Precision Medicine Group

Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, scripting, Object Oriented Programming, clinical research, programming, CDISC standards, database management
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Precision For Medicine

Skills & Focus: clinical database management, clinical research, data management, EDC vendor, programming, scripting, CDISC standards, object-oriented programming, clinical research tasks, biomarkers
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline; Medidata Rave EDC Certified Study Builder; Rave API integration experience.

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Research, Project Management, Medical Coding, EDC, SOPs
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Precision For Medicine

Skills & Focus: Clinical Database Manager, clinical data management, EDC vendor, Medidata Rave, Rave API, programming, scripting, CDISC standards, drug development, clinical research
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
Skills & Focus: clinical database management, clinical data management, EDC, data management, clinical research, programming, scripting, CDISC standards, drug development, object-oriented programming
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Precision Medicine Group

Skills & Focus: clinical databases, Data Management, EDC vendor, operational training, programming, clinical research, Object Oriented Programming, scripting language, CDISC standards, database management systems
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…

Precision For Medicine

Skills & Focus: clinical studies, protocol expertise, investigator meetings, regulatory submissions, site visits, oncology, quality outcomes, risk mitigation, conflict resolution, study monitoring
About the Company: Precision for Medicine is a CRO passionate about cultivating culture with high CRA retention rates, allowing employees to have an influence and support from ma…
Experience: 2 years or more as a CRA in a CRO or pharmaceutical/biotech industry.

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Protocol, Training, Documentation, Medical Coding, SOP Development
Experience: Bachelors and/or a combination of related experience; Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Astrazeneca

Skills & Focus: program ownership, global development strategy, oncology, drug development, clinical plans, project management, regulatory influence, collaborative, leadership, biopharmaceutical
About the Company: AstraZeneca is a global pharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. They are committed to im…
Experience: Ten (10)+ years in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology
Type: Full-time

Veeva Systems

Skills & Focus: Team Manager, Veeva RIM, Professional Services, implementation, consultants, coaching, life sciences, regulatory processes, project management, data management
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: 8+ years of hands-on software implementation experience at a software vendor or consulting firm within the life sciences R&D or healthcare space, 2+ years experience of managing professional services consultants
Benefits: Employees are shareholders; Veeva Giving program supports charitable causes; strong stance against non-compete agreemen…

Parexel

Senior Medical Writer Kingdom of Spain
Skills & Focus: medical writing, clinical research, biopharmaceutical, drug development, medical content, medical documents, clinical trials, regulatory submissions, technical writing, medical communications
About the Company: Parexel is a global clinical research organization that provides a range of services to help biopharmaceutical companies develop new drugs and medical treatmen…
Skills & Focus: Clinical Trials, Investigator Contracts, Spain, FSP, Remote Work, Biopharmaceutical, Regulatory Affairs, Patient Experience, Consulting, Medical Writing
About the Company: Parexel is a global biopharmaceutical services organization that provides solutions in consulting, clinical research, and commercialization. The company specia…
Type: Full-time
Skills & Focus: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.

Precisionmedicinegroup

Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, client information, feasibility site outreach, post-award feasibility, patient advocacy groups, enrollment modeling, clinical trial
Experience: 5 years

Pfm

Skills & Focus: clinical, data, management, database, protocol, CRF, UAT, bioinformatics, regulatory, healthcare
Skills & Focus: clinical, data, management, database, protocol, CRF, UAT, bioinformatics, regulatory, healthcare

Iqvia

Study Start Up Lead Kingdom of Spain
Skills & Focus: site activation, clinical trials, regulatory compliance, project management, biotechnology, clinical practice guidelines, study initiation, budget planning, contract negotiation, regulatory intelligence
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 7 years relevant experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Pfm

Skills & Focus: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
Experience: 5 years

Iqvia

Skills & Focus: clinical trial management, global coordination, vendor management, stakeholder engagement, compliance, GCP, trial execution, budget monitoring, data management, issue resolution
About the Company: IQVIA is a leading global provider of information, innovative technology solutions, and contract research services focused on the healthcare industry.
Experience: 6-8 years clinical trial management experience in the pharmaceutical industry or CRO.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.