Sarah Rawlings Email and Phone Number
Sarah Rawlings work email
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Sarah Rawlings personal email
First class degree in biology.Demonstrated interpersonal and leadership skills, effective communication, proactive and self disciplined.over 20 years experience in Clinical Research. Therapeutic areas: Auto-immune, migraine, cluster headache, diabetes, urology, osteoporosis, hip fracture, retinopathy, psoriasis, oncology ( phase 1-3).Skills: Experience in global clinical trial management, site selection, Investigator relationship management, site activation, Clinical Trial Application (CTA) form, Voluntary Harmonisation Process (VHP), Eu CTR, Investigator meeting and training, enrollment, clinical trial monitoring, risk based monitoring, risk assessment, database lock, study close out, MHRA Inspections, CRO oversight, line management, portfolio management.2 years experience in Pharmacovigilance.
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Study LeadIqvia Nov 2023 - Present -
Associate Global Trial DirectorIqvia Nov 2020 - Oct 2023United Kingdom
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Expert Global Trial ManagerIqvia Jul 2020 - Oct 2020United Kingdom
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Senior Global Clinical Trial ManagerIqvia Jan 2019 - Jul 2020As a senior GTM I am working in phase 1 oncology managing the monitoring vendor.
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Regional Lead Site Activation ManagementEli Lilly And Company Feb 2017 - Nov 2018BasingstokeAs regional Lead Site Activation Manager I am accountable for the planning and implementation of the regional (EMEA) site start up, maintenance, and close out plan. I partner with the global and regional cross functional team to ensure accurate planning and timely execution of country and site level site activation management milestones in alignment with quality standards, leveraging my project management, and site activation expertise to achieve these deliverables, and providing clinical operational expertise to internal and external customers/business partners. -
Workstream Lead For Site Risk AssessmentEli Lilly And Company Sep 2016 - Jul 2018BasingstokeRisk based monitoring is an adaptive approach to clinical trial monitoring that directs monitoring focus and activities to the evolving areas of greatest need which have the most potential to impact subject safety and data quality. I have been responsible for the implementation of site risk assessment, which is a new initiative taking risk based monitoring to the next level. I co-ordinate the implementation both internally within Lilly and with our third party central monitoring and site monitoring vendors. Through site risk assessment we determine the specific monitoring frequency and mitigation strategies (site specific monitoring requirements) at the start of the trial for all selected sites.
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Country Studies ManagementEli Lilly And Company Ltd Jun 2011 - Feb 2017BasingstokeI provided clinical operational expertise through regional clinical trial management. I was responsible forglobal/regional site activation, co-ordinating and facilitating enrollment readiness to plan, including project management of supplies, system set up, regional investigator meeting planning/logistics/agenda and hosting the live meeting. I was also responsible for global/regional enrolment delivery to plan partnering with leadership and affiliate staff, as well as co-ordinating investigator site communications and enrolment acceleration programs.
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Clinical Development ConsultantEli Lilly And Company Oct 2014 - Feb 2015BasingstokeShort Term Assignment to cover gap in resource. Provided operational expertise to customers through ownership of site performance from site selection through site close out in the UK for all biomedicines trials. Responsible for managing issue escalation and oversight of trial sites monitored by third party vendor. Selected trial sites for migraine and cluster headache research.
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Clinical Operations Portfolio ManagerEli Lilly And Company Jul 2013 - Feb 2014BasingstokeMaternity leave cover. Responsible for the delivery of the biomedicines clinical trial portfolio in Europe. Responsibilities included, managing the clinical trial allocation strategy, regional input into study design, co-ordinated feasibility and site selection process for new trials.
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Regional Clinical Trial ManagerEli Lilly And Company Nov 2009 - Jan 2011BasingstokeRegional Clinical Trial Manager. Responsible for trial delivery in Europe.
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Principal Clinical Research AssociateEli Lilly And Company Jan 2006 - Nov 2009BasingstokeClinical Research Associate with project lead responsibilities.
Sarah Rawlings Skills
Sarah Rawlings Education Details
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Biology, General
Frequently Asked Questions about Sarah Rawlings
What company does Sarah Rawlings work for?
Sarah Rawlings works for Iqvia
What is Sarah Rawlings's role at the current company?
Sarah Rawlings's current role is Study Lead at IQVIA.
What is Sarah Rawlings's email address?
Sarah Rawlings's email address is ra****@****lly.com
What schools did Sarah Rawlings attend?
Sarah Rawlings attended University Of Plymouth.
What skills is Sarah Rawlings known for?
Sarah Rawlings has skills like Clinical Development, Clinical Trial Management System, Clinical Trials, Clinical Research, Pharmaceutical Industry, Good Clinical Practice, Clinical Monitoring, Cro Management, Therapeutic Areas, Diabetes, Electronic Data Capture, Pharmacovigilance.
Who are Sarah Rawlings's colleagues?
Sarah Rawlings's colleagues are Ramya B E, Ning Wang, Mariana Kabasanova, Lina Pang, Gayatry Shivam, Florence Puno, Romina Mermelstein.
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Sarah Rawlings
Head Of Service Operations Leading Customer Service Excellence At SimplyhealthUnited Kingdom1simplyhealth.co.uk -
1kcl.ac.uk
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