23 Biopharmaceutical Leadership jobs in Bucharest.

Bucharest

• Skills: Data Management, Clinical Programming, Remote, FSP, Biomedical Research, Clinical Trials, Data Acquisition, Statistical Programming, Global Inclusion, Biometrics

Bucharest

• Skills: Clinical Research, Trial Master File, Clinical Trials, Documentation, Project Timelines, Regulatory, Start-Up, Data Management, Communication, Organizational Skills
• Experience: Clinical research administrative support experience preferred
• Type: Full time

Bucharest

• Skills: medical review, adverse events, safety signaling, stakeholder insight, negotiation skills, strategic planning, complaints monitoring, clinical investigation, data entry, medical device regulations
• Experience: At least 5 years of medical professional experience, including 2 years related clinical, safety, pharmacovigilance or regulatory experience in the medical device industry.

Bucharest

• Skills: clinical site monitoring, training, CRA skills, protocol compliance, SOP compliance, regulatory compliance, site management, investigative site, patient recruitment, data monitoring
• Type: Full-time

Bucharest

• Skills: Pharmacovigilance, ICSR, SAE, Risk Management, Safety Reports, Clinical Trials, Benefit-Risk Assessment, Signal Detection, Regulatory Compliance, Drug Safety
• Experience: 3+ years in pharmacovigilance
• Type: Full-time
• Salary: Competitive

Bucharest

• Skills: Pharmacovigilance, ICSRs, signal detection, risk management, QPPV, adverse events, medical review, Safety Reports, regulatory authority, mentoring

Bucharest

• Skills: Regulatory Affairs, Consulting, Global Asset Lead, Clinical Research, Pharmaceutical, Biotechnology, Project Leader, Data Management, Statistical Programming, Biostatistics
• Type: Consulting

Bucharest

• Skills: PMS activities, post market strategy, product safety issues, regulatory authorities, regulatory intelligence, compliance activities, SOPs development, continuous improvement, training materials, medical device regulations
• Experience: Minimum 2 years’ experience
• Type: Full Time

Bucharest

• Skills: medical monitoring, clinical studies, patient safety, clinical development, data safety monitoring, clinical data analysis, SAE reports, medical review, clinical training, risk assessment

Bucharest

• Skills: Clinical Project Manager, Clinical research, Project Management, Compliance, Regulatory submissions, Interdisciplinary project tasks, Stakeholder training, Data management, Patient safety, Team performance
• Experience: 1-3 years of experience in clinical study management
• Type: Full-time, Permanent

Bucharest

• Skills: adverse reactions, medical representatives, benefits and risks, medicinal product, evaluation, safety studies, safety profiles, emerging safety concerns, marketing authorisations, overview

Bucharest

• Skills: pharmacovigilance, case processing, medical information, regulatory affairs, quality assurance, individual case safety reports, clinical trials, mentoring, safety data, biotechnology
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