22 Biopharmaceutical Leadership jobs in Remote - Kingdom of Spain.

Hiring now: Risk Surveillance Lead Fs @ Parexel, Regulatory And Start Up S @ Precision , Associate Dir Coa Managem @ Iqvia, Site Contracts Spec Ii Or @ Syneos Hea, Srprincipal Clinical Data @ Precision , Team Mgr Veeva Rim Profes @ Veeva Syst, Clinical Prod Spec @ Avanos Med.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (7) Clinical Research (5) Project Management (4) clinical research (4) CDISC standards (4) data management (3) EDC vendor (3) programming (3) project management (3) Data Management (3)

📍 Locations

Kingdom of Spain (22)

Parexel

Skills & Focus: Project Leadership, Risk Surveillance, FSP, Clinical Research, Project Plans, SOPs, ICH, GCP, Compliance, Budget

Precision For Medicine

Skills & Focus: Regulatory, Site Activation, Budget Negotiation, Feasibility, Clinical Operations, Project Management, Site Contracts, Communication Skills, Electronic Spreadsheets, Spanish Fluency
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help th…
Experience: 1 year or more as a Regulatory/ SU specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies.
Type: Full-time
Skills & Focus: Clinical Trials, Oncology Standards, Data Cleaning, Clinical Research, Electronic Data Capture (EDC), Data Review, Medical Monitor, Cross-functional Communication, User Acceptance Testing (UAT), Clinical Data Review Guidelines
About the Company: Precision Medicine Group, LLC is an Equal Opportunity Employer focused on the life sciences and healthcare sectors.
Experience: Minimum of 8 years of clinical research experience; Minimum of 1 year of leadership experience
Type: Remote
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.

Iqvia

Skills & Focus: COA Management, Patient Centered Solutions, Clinical Trials, Consulting, Health Technology Assessments, Product Lifecycle Management, Market Access, Research, Stakeholder Engagement, Financial Management
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: 8-10 years total work experience with 5+ years in the pharmaceutical/medical device industry.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
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

Syneos Health

Skills & Focus: contract management, clinical trials, negotiating contracts, budget preparation, quality control, project management, vendor management, clinical protocols, customer-focused, communication skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: High level of contracts management experience. Experience in a contract research organization or pharmaceutical industry essential.
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

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

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…
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

Iqvia

Skills & Focus: clinical trial management, study management team, project planning, risk mitigation, compliance, stakeholder management, data collection, vendor oversight, document management, training materials
About the Company: IQVIA is working to create a healthier world through diverse expertise, innovation, and powerful capabilities in the healthcare sector.
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.
Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, Good Clinical Practice
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: 2-5 years of experience in managing late phase clinical trials at global level
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

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…

Syneos Health

Skills & Focus: Clinical Regulatory Affairs, Oncology, Site Start-Up, Patient Enrollment, Project Management, Clinical Trial, Regulatory Activities, Clinical Research, Risk Management, Vendor Management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum 6 years CRO industry experience and/or a minimum 5 years’ experience working in a SSU, or clinical trial environment.
Skills & Focus: medical writing, regulatory writing, clinical study reports, lay summaries, plain language summaries, patient information, quality checks, document preparation, health literacy, clinical research
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Minimum 2 years of regulatory writing experience.

Precision Medicine Group

Skills & Focus: Clinical Data Management, Database Development, Data Quality Control, Clinical Trials, Regulatory Compliance, Project Management, Data Entry Guidelines, Medical Coding, SOP Development, Stakeholder Communication
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Type: Remote

Parexel

Skills & Focus: Clinical Research, Monitoring, Site Management, Patient Safety, Clinical Trials, Project Management, Quality Assurance, Regulatory Compliance, Stakeholder Engagement, Investigator Relations
Experience: 5 years of clinical research experience and/or quality management experience.

Syneos Health

Skills & Focus: quality control, clinical documents, copyedit, proofread, format, data content, clinical study protocols, submission standards, attention to detail, EDMS
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Must be performing at Senior level.
Benefits: We are passionate about developing our people, through career development and progression; supportive and engaged line …

Precision Medicine Group

Skills & Focus: Clinical Data Management, Oncology, Orphan Drug, Database Development, Quality Control, CRF specifications, SOPs, Data Entry Guidelines, CDISC standards, Medical Coding
About the Company: Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation,…
Experience: 8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner
Skills & Focus: Functional Service Provider, Clinical Trials, Site Care Partner, CRA, Clinical Research Associate, Project Leader, Biostatistics, Regulatory Affairs, Data Management, Statistical Programming
About the Company: Parexel helps accelerate the development of new medical treatments and therapies.
Type: Full-time

Avanos Medical

Skills & Focus: training, healthcare professionals, medical devices, product evaluations, customer support, technical issues, presentations, workshops, interpersonal skills, clinical practice
About the Company: Avanos Medical is a medical device company focused on delivering clinically superior breakthrough solutions that helps patients recover post-surgery. The organ…
Experience: Minimum 5 years of relevant experience in a similar role
Type: Full-time