Lauren Skogen Email & Phone Number

United States

Evansville, Indiana, United States

Evansville, Indiana Area

Tampa, Fl

I work with candidates in the Medical Imaging field looking to achieve career growth.

Newburgh, In

I specialize in Clinical R&D, Capital Imaging Equipment Sales and Services in Medical Imaging. I am eager to make the perfect match between clients and candidates. I represent highly qualified professionals to top-tiered companies. I build strong relationships with my candidates and customers to identify key professionals who excel in the Medical Imaging, Clinical Research, and Biomedical Industry. I have over 15 years experience working in healthcare and clinical research among some of the best talent in the Industry. My vast knowledge of Medical Imaging and Biomedical Services was gained by working for CRO's, Sponsor companies, Biotech companies, Nutritional companies, and Medical Device companies.

Bowling Green, Ky

Family owned franchise clothing boutique.

Home Based

Coordinate the marketing, business development, contract and budget development/negotiations, and grant management activities for the GEMMS Cardiovascular Research Consortium

Coordinated and supervised cardiovascular clinical research trial project timelines throughout all lifecycle phasesProvided leadership in the development of cardiovascular trials and related documentsDeveloped a network of Investigators, research directors, clinical trial sponsors, study teams, and outside consultantsDefined and managed project resource needs and established contingency plans for key resourcesPlanned trial budgets, communicated deviations, and proposed solutions for delays and deviationsCreated integrated project timelines and tracked performance metrics for trial teamsTracked and managed study managers across trial teamsIdentified and presented project related issues and facilitated resolutionsProvided proactive and creative recommendations on how to meet goals and handle deviationsDeveloped project status reports and communicated with all applicable team members involvedBuilt and maintained strong pharmaceutical industry sponsor and organizational team relationships for the success of clinical trial managementSupported clinical operations to ensure clinical trial resources were developed, estimated, and reported accurately and timelyInitiated improvements to enhance the efficiency and quality of work performed on projectsCommunicated and escalated unresolved issues to the appropriate level of managementEnsured all staff adhered to professional standards and SOPs established for clinical research

Developed, monitored, and managed clinical studies with a team approachAssisted in protocol development, created source documents and case report formsEnsured clinical product and study supplies were available for global sitesMaintained study compliance with Good Clinical Practices and Mead Johnson proceduresManaged the Investigator Initiated Trial Program, including budgets, scope, and feasibilityRegistered and updated clinical trials on the government websiteManaged key outcomes, timelines, and project deliverables for assigned projectsWrote Informed Consent forms and study documents for IRB submissionsReviewed and approved central IRB documentsNegotiated, approved, and tracked study budgets with global clinical sitesServed as primary contact for protocol clarifications and project logistics for assigned projects

Served as the primary communicator and liaison interdepartmentally, between research facility and pharmaceutical sponsor for assigned clinical trialsDeveloped source documents and Informed Consent Forms for assigned projectsManaged and provided leadership for the entire study from initiation to close-out and assumed responsibility for overall conduct of the assigned clinical trial on a daily basisEnsured requirements were met in accordance with FDA guidelines, ICH guidelines, Good Clinical Practices, Sponsor Specifications, and Covance Procedures for multiple protocolsManaged multiple projects at different stages of the clinical research processPlanned and managed the feasibility, scope, and study timelines of projectsPresented staff meetings, staff training, and client meetingsDirected monitors on site visit and monitoring plansPerformed phlebotomy, vital sign measurements, holter monitoring, ECG recordings, medical writing, spirometry, and adverse event assessmentsReceived perfect score surveys for maintaining exceptional client satisfaction Increased company profits by generating repeat business with several large clients

Biology And Chemistry

Education record

Education record