Drug Adverse Events Stellenangebote


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3 Jobs für Drug Adverse Events


Stellenangebote Drug Adverse Events Jobs


Job vor 14 Tagen bei Mindmatch.ai gefunden Neurocrine Biosciences

Medical Director Endocrinology Europe, MD

• AT- 2 Schweiz Führungs-/ Leitungspositionen [. .. ] clinical data interpretation, site and PI interaction, regulatory response documents, ongoing safety review, and medically relevant vendor and operational deliverables. Works cross-functionally with Clinical Operations, Regulatory, Biostatistics, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Data Management, Drug Safety, Clinical Pharmacology, Translational Medicine, Medical Writing, vendors, and investigators to ensure clinical accuracy, participant safety, protocol alignment, and timely execution of study deliverables across Phase 1-4 programs. # # Your Contributions (include, but are not limited to) : Provide medical and scientific input into clinical study designs, [. .. ] data, protocol deviations, concomitant medications, data review meeting materials, and other emerging clinical data to identify potential safety signals, data-quality issues, or clinically relevant trends Provide medical interpretation of adverse events, laboratory abnormalities, safety trends, and clinically relevant subject-level data; escalate participant-safety, study-integrity, or decision-critical issues when appropriate Review study-related vendor manuals, process documents, data-transfer specifications, assessment plans, imaging or device instructions, patient-facing materials, and site guidance for medical appropriateness, protocol alignment, feasibility, and [. .. ]

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Job am 21.07.2026 bei Mindmatch.ai gefunden Bristol- Myers Squibb

Director, Global Clinical Physician Boudry-CH R1602576 Posted 21 hours ago

• AT- 2 Schweiz Führungs-/ Leitungspositionen [. .. ] careers. bms. com/working-with-us. Functional Area Description The Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. Position Summary/ Objective Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities [. .. ] responsibility for site interactions in partnership with the Global Clinical Scientist (GCS) for medical questions and education (including safety management guidelines) Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives Collaborates with GCS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/ exclusion and other safety-related clinical considerations) Fulfills GCP and compliance obligations for clinical conduct and maintains all required training Clinical Development Expertise [. .. ]

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Job vor 2 Tagen bei Neuvoo.com gefunden IQVIA

Associate Medical Director, Cardiology, with Metabolic Diseases and Nephrology Experience

Führungs-/ Leitungspositionen [. .. ] investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/ exclusion determinations, and issues of patient safety and/or eligibility. Performs medical review of the protocol, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Investigative Drug Brochure (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance department. May perform [. .. ]

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