Lia Loime work email
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Lia Loime personal email
20+ years experience in clinical research in both the pharma and medical device industry as a CRA, Clinical Trials Lead and Site Coordinator. I have experience in managing trials with different indications for different Clients. I have worked as a Clinical Research Associate (Monitor) in Estonia and also have monitoring experience in Latvia, Lithuania, Ukraine, UK, Slovenia and Sweden. I have been as a Clinical Lead/Clinical Operations Leader in CRO. Since Sep 2016 I work as a freelancer CRA.Therapeutic areas of expertise include oncology (CLL, colorectal, prostatic, pancreatic, head & neck and breast cancer), infectious diseases (tuberculosis), neurology (MS, epilepsy, stroke), rheumatology (PSA), endocrinology (diabetes), psychiatry (depression, schizophrenia), cardiology (CHF, arrhythmia, acute MI), dermatology (acne, psoriasis), intensive care (sedation) and osteoporosis. I have experience in device studies (head & neck, breast and pancreatic cancer; acute MI – CE and non-CE marked).I am currently based in Estonia and I am available to work as a freelancer CRA, Clinical Lead or clinical research consultant.
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MdAs Valga Haigla Feb 1998 - PresentValga, EstoniaEndoscopy doctor
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Clinical Research Associate/ConsultantEgeen International Inc. Nov 2016 - PresentTartu, EstoniaTraining and mentoring CRAs, performing co-monitoring visits, reviewing monitoring reports, assisting in quality control.
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Senior Clinical Research AssociateZoll Circulation Sep 2016 - PresentEstoniaResponsibilities include monitoring clinical trial in accordance with the ICH-GCP, EU Directives and local regulations in Estonia and in other countries within European Union (Latvia, Slovenia; Sweden). Responsibilities include preparation and submission of documentation to Ethics Committee and Regulatory Authorities in Estonia, Latvia and Sweden, coordination of financial negotiations between contractors (hospital/investigator and sponsor), facilitating site training and initiation, monitoring, data collection, and close out. Tracking site payments and closing investigations with EC and RA. Performing the site close out visits in UK and in other countries within European Union as needed.
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Study Site CoordinatorTartu University Hospital Jun 2008 - Mar 2017Tartu, EstoniaResponsibilities included training and assisting the investigational site. -
Senior Clinical Research AssociateCrown Cro Nov 2007 - Jun 2016Tartu, EstoniaResponsibilities included monitoring clinical trials in accordance with the ICH-GCP, EU Directives and local regulations in Estonia and in other countries within European Union. Responsibilities included identification, selection and qualification of investigational sites for various international trials, preparation and submission of documentation to Ethics Committee and Regulatory Authorities in Estonia, coordination of financial negotiations between contractors (hospital/investigator and Crown CRO), facilitating site training and initiation, monitoring and data collection, and close out. Tracking site payments and closing investigations with EC and RA. Training and mentoring new CRAs and CRA Assistances, performed co-monitoring visits with other CRAs. -
Clinical Research Associate / Clinical Trials LeadEgeen International Inc. May 2004 - Sep 2007Tartu, EstoniaResponsibilities included investigational sites qualification, initiation, monitoring, termination and general management ensuring compliance with the ICH-GCP, FDA, EU Directives and local regulations, monitoring guidelines and SOPs. Acting as a Clinical Lead with reviewing site visit reports, hosting CRA team teleconferences and developing monitoring tools, company’s SOPs. Mentoring and performing assessment and training visits with CRAs, interviewing and training new CRAs.Responsibilities included training and assisting the investigational site.
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Senior Clinical Research AssociateParexel Aug 1998 - Apr 2004Estonia (Parexel Medstat, Parexel Baltic As)Responsibilities included monitoring clinical trials in accordance with the ICH-GCP and local regulations in Estonia and in other countries within European Union. As a local Country Specialist my responsibilities included identification, selection and qualification of investigational sites for various international trials, preparation and submission of documentation to Ethics Committee and Regulatory Authorities in Estonia, coordination of financial negotiations between contractors (hospital/investigator and PAREXEL), facilitating site training and initiation, monitoring and data collection, and close out. Tracking site payments and closing investigations with EC and RA. Participation in audits.Training and mentoring new CRAs and CRA Assistances, performed co-monitoring visits with less experienced CRAs or at problem sites. -
MdTartu University Hospital Jun 1989 - Jan 2000EstoniaSurgeon in Department of General Surgery, Tartu University Hospital (1989-1993); lecturer of surgical anatomy (1998-2000)
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Clinical Research AssociateMederes As Jan 1995 - Jan 1996Tartu, EstoniaInitial employment in the position Co- CRA and then working as a CRA within 1 year. Responsibilities included site monitoring, closeout of phase III clinical research studies, conducted according to the ICH/GCP Guidelines in the Estonia.
Lia Loime Education Details
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Doctor Of Medicine (M.D.)
Frequently Asked Questions about Lia Loime
What company does Lia Loime work for?
Lia Loime works for Egeen International Inc.
What is Lia Loime's role at the current company?
Lia Loime's current role is MD at AS Valga Haigla.
What is Lia Loime's email address?
Lia Loime's email address is li****@****cro.com
What schools did Lia Loime attend?
Lia Loime attended University Of Tartu.
Who are Lia Loime's colleagues?
Lia Loime's colleagues are Anca Cristache, Shanta Koendjbiharie.
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