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Planning - Medizinische, Gesundheit Stellenangebote suchen & aufgeben Planning
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Medical Advisor (m/f/d)
To strengthen our team in the area of Medicine in the Medicine & Research department, we are immediately looking for a Medical Advisor (m/f/d) Your essential tasks Supervising clinical studies with responsibility for the medical content and patient safety, including medical monitoring, pharmacovigilance and evaluation of reference documents Giving medical advice to external study physicians and internal project partners on all studies and projects conducted by GBG Planning and drafting study protocols and amendments, writing clinical study reports and development safety update reports Collaborating in scientific contributions for leading international congresses and publications with global reach on clinical studies and translational research projects Opportunity to conduct and publish your own scientific work Regular active participation in our subboard meetings with external key opinion leaders Regular active participation in internal and external training events, including speaking engagements Your profile You have successfully completed a degree in human medicine and have completed specialist training in gynecology & obstetrics or internal medicine - ideally with experience in gynecologic oncology and / or hemato-oncology Alternatively, you have successfully completed a degree in pharmacy and have relevant experience in the conduct of pharmaceutical trials in oncology You have experience with scientific work and clinical trials including work according to Good Clinical Practice (GCP) You enjoy working independently in highly motivated and dynamic team You have the following skills: strong communication skills, analytical working and thinking skills, as well as a very good organizational and time management You are tech savvy and confident in using MS Office applications, as well as MS Teams and reference management software (e.g.Partner-Anzeige20.06.202463263 Neu IsenburgMedizin, Gesundheit -
1
Medical Advisor (m/f/d)
To strengthen our team in the area of Medicine in the Medicine & Research department, we are immediately looking for a Medical Advisor (m/f/d) Your essential tasks Supervising clinical studies with responsibility for the medical content and patient safety, including medical monitoring, pharmacovigilance and evaluation of reference documents Giving medical advice to external study physicians and internal project partners on all studies and projects conducted by GBG Planning and drafting study protocols and amendments, writing clinical study reports and development safety update reports Collaborating in scientific contributions for leading international congresses and publications with global reach on clinical studies and translational research projects Opportunity to conduct and publish your own scientific work Regular active participation in our subboard meetings with external key opinion leaders Regular active participation in internal and external training events, including speaking engagements Your profile You have successfully completed a degree in human medicine and have completed specialist training in gynecology & obstetrics or internal medicine - ideally with experience in gynecologic oncology and / or hemato-oncology Alternatively, you have successfully completed a degree in pharmacy and have relevant experience in the conduct of pharmaceutical trials in oncology You have experience with scientific work and clinical trials including work according to Ausschreibendes Unternehmen: GBG Forschungs GmbH Ausschreibungsdatum: 2024-06-15 Vertragsart: Festanstellung Vollzeit Tätigkeitsbereich(e): Medizinische Forschung; Pharmazie; Medizin, Pflege; Arzt Branchen: Gesundheitsdienstleistungen; Wissenschaft & ForschungPartner-Anzeige20.06.202463263 Neu IsenburgMedizin, Gesundheit -
1Provide medical leadership for a gastroenterology development candidateLead, perform, and coordinate clinical drug development activitiesEngage closely with medical advisory board members and key medical experts in gastroenterologyPlan clinical trials in collaboration with key physicians, integrating their feedback to enhance project planning and executionSelect medical indications and conduct in-depth analysis of medical needs, clinical endpoints, and the competitive landscapeContinuously review study data, making strategic recommendations to meet project goalsDevelop and refine clinical protocols, overseeing medical monitoring and ongoing medical data review, including protocol exemptions, violations, and eligibility issuesManage pharmacovigilance for assigned projects and oversee ongoing safety reviews, including monitoring adverse events and lab abnormalitiesMaintain and enhance medical advisor activitiesCollaborate on regulatory submissions, providing essential input for regulatory documentsSupervise a Clinical Project Assistant for designated activitiesYour profileMedical degree (MD) or an advanced degree in science or medicine with significant experience in medical monitoring rolesExtensive experience in clinical trials within CROs, sponsors, or clinical sites, preferably in gastroenterologyProven experience in protocol development and engagement with key opinion leadersDemonstrated leadership in managing projectsAbility to work self-directed, drive processes, and excel in project management.Partner-Anzeige05.06.2024Medizin, Gesundheit
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