Stephanie Lankhorst Email & Phone Number

Haarlem, Nh, Nl

Amsterdam, Noord-Holland, Nederland

Faculteit Geneeskunde VU

Monitoring if the execution and documentation of investigator initiated clinical studies are in line with the WMO, GCP, ISO4155, AmsterdamUMC Research Code, protocol, SOPs, and other relevant guidelines and legislation.Responsibilities: monitoring & study support, quality control & support, project management, mentoring & training of newly appointed/less experienced CRA’s

Amsterdam Area, Netherlands

Haarlem, Noord-Holland, Nederland

Amsterdam Area, Netherlands

Responsibilities:Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.• Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Build awareness of features and opportunities of study to site.• Collaborate and liaise with study team members for project execution support as appropriate.

Amsterdam Area, Netherlands

Responsibilities:- Complete appropriate therapeutic, protocol and clinical research training to perform job duties.- Gain experience in study procedures by working with experienced clinical staff.- Under close supervision, perform site selection (if applicable), initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices.- If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas to CRA for improving site recruitment plan in line with project needs to enhance predictability. Assist CRA in tracking subject site recruitment progress.- Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.- Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. Under close supervision may support start-up phase.- Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.- Convey features and opportunities of study to site.- Collaborate and liaise with study team members for project execution support as appropriate.

Rotterdam Area, Netherlands

Thesis: Hypertension and renal toxicity during angiogenesis inhibition: salt dependency and treatment optionsDepartment of Internal Medicine, division Pharmacology & Vascular MedicineResponsibilities: - design, perform and analysis of (pre)clinical studies- writing and publishing of scientific papers in high impact journals- taking care of education and supervising medical and internship students- Communication between executive parties; laboratory, pharmacy and clinicians (dept. of Internal Medicine, Nephrology and Oncology )- both national and international oral presentations for a varied audience

Rotterdam Area, Netherlands

Imaging of Thoracic Aortic Aneurysms Department of Internal Medicine, division Pharmacology and Vascular Medicine

Amsterdam Area, Netherlands

Right Ventricle adaptation in Pulmonary Hypertension, Department of Pulmonology and PhysiologyInclusion en data analysis of phase 4 clinical trial ‘Intravenous Iron Treatment In Iron Deficient Patients With Idiopathic Pulmonary Arterial Hypertension’ (NCT01288651)

Phd (Dr)

COEUR conducts innovative research and provides high quality training in the cardiovascular field. The research programs include a wide.

Msc, Top Master'S Programme In Cardiovascular Research

Clinical and Biophysical Aspects of Heart and Circulation, Pathophysiology of Heart and Circulation, Remodelling of the Circulatory.

Bsc, Bachelor'S Degree In Biomedical Sciences

Areas of specialisation include: International Public Health, Oncology

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