Eunice Lafko Email & Phone Number

Wilmington, Nc, Us

Wilmington, Nc, Us

Waltham, Ma, Us

Waltham, Ma, Us

Raleigh, North Carolina, Us

1. Project Administration- Utilizes clinical trial management systems to track and process trial information to provide analysis of information to PM and customers. Processes and tracks invoices and investigator grants payments. Assists with managing the executed contract and financial aspects of assigned projects. Reviews study budgets and expenses to ensure all study related contractual and budgeting issues are upheld and performed. Oversees regulatory documentation and submission process. Ensures project documentation, including Trial Master File, are complete and audit ready. Assist PM with study plan updates and review.2. Reporting- Records Key Performance Indicators (KPIs) in assigned systems, with oversight from the PM. Prepares and provides status reports to customers with oversight from assigned PM. Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing, and tracking reports, and functional area plans to appropriate team members and senior management.3. Communication- Schedules and attends internal and external team meetings. May lead internal team meetings and portions of external team meetings as directed by assigned PM. Prepares and distributes agendas and minutes for both internal and external meetings. Follows-up with team members on action items from meetings. Prepares for and attends Investigator Meetings, Kick-Off Meetings, Quick Start Camps, and Quality Finish Camps. 4. Training- Facilitates team training in accordance with protocol and/or project requirements, including therapeutic, protocol specific, and process training.5. Project Leadership - May serve as primary customer contact when PM is out of the office. Acts as a liaison and facilitator between other departments within the company to ensure project related tasks and/or issues are addressed.6. Acts as Administrator of shared workspace for assigned projects.

Basel, Baselstadt, Ch

1. Support Study Leads in ensuring all trial deliverables are met according to timelines, budget, operational procedures and quality standards.2. Support CTLs by setting up and maintaining appropriate study tracking forms.3. Support the CTLs in drafting the ICF global template; format and arrange printing of protocols and IBs; and track protocol amendments and IB updates.4. Support CTL with all US drug supply shipping (initial and re-supply) to local CPO and all US sites. Function as the liaison with vendor to ensure drug delivery and relabeling occur in a timely fashion and track all drug at the central hubs. Support CTLs in all drug tracking to ensure adequate supply, monitor expiration dates and assist in relabeling as appropriate. Support CTL in tracking all batch numbers used throughout trials and assist with preparation of appropriate CSR appendix. 5. Manage and track US invoices for third party vendors. Process all US third party vendor payments. Function as a liaison between third party vendor and finance to resolve issues and discrepancies.6. Supports the Study Lead for US operational activities including working closely with US Clinical Operations for US study start-up activities. Is primary contact for the US sites for operational issues.7. Set up and maintain electronic Trial Master File (eTMF) tracker in CREDI for all studies. Provide support to CTL to ensure timely completion of eTMF tracker for CSR.8. Support CTL in delegated aspects of trial data analysis and reporting including attendance at all relevant study meetings (i.e., CTT and dose escalation meetings). 9. Assist CTL with preparation and distribution of study tools needed at study start up and throughout trial as appropriate.10. Support the Study Lead with all sample and data tracking in collaboration with the Clinical Information Technology (IT) Specialist and act as a liaison with sites for sample shipment, sample reconciliation and associated logistics.

Brookline, Massachusetts, Us

• Perform initial eye exam workups for patients.• Perform various eye exam testing, including eye refraction, pressure test, Lasik Evaluations, Glaucoma and Cataracts testing, etc.• Assist Doctors in Lasik and other eye surgeries and procedures, including injections and blepharoplasty.• Work with Sponsor Clinical Monitor to initiate Clinical Trial Study.• Perform duties as Study Coordinator to obtain IRB approval.• Coordinate with Clinical Monitor and study Investigators to obtain necessary documentation to prepare for clinical trial.• Certifications: VISX WaveScan WaveFront System, VISX Eximer Laser System, IntraLase Femtosecond Technology, CITI Good Clinical Practice (GCP) Basic Course, CITI IRB Member Basic Course, CITI IRB Members Basic/Refresher Course.• Equipment: Pentacam, Specular, IOL Master, OCT, Atlas, WaveScan, Eximer Laser, IntraLase, Auto-refractor, Auto-phoropter, Tonopen, Colvard.

• Research market viability for client’s proposed product.• Write up formal report on research findings.

Boston, Ma, Us

Boston, Ma, Us

• Study the effect of enzyme digestion (namely collagenase) and mechanical stretch on the mechanical properties of mice lung tissue at multiple length scales.• Use light, confocal, and electron microscopy to visualize effects of digestion and stretch on extracellular matrix fibers (i.e. collagen).• Use Fluorescent Recovery After Photobleaching (FRAP) to analyze diffusion and binding kinetics of collagenase.• Use Western Blot and gel electrophoresis to analyze effects of enzyme digestion on collagen content.• Use Network Simulation Program to model and simulate experimental findings.• Attend various conferences and present current research findings

• Used the computer programs Amira and IA-FEMesh to construct models of mechanically manipulated bone fractures based on μCT scans• Used models to simulate mechanical manipulation of fractures and compare to experimental results

• Completed a preliminary study in characterizing a trend in residual strain in porcine pulmonary trunks.• Assisted in troubleshooting a bending device to make it ready for use.• Attended classes covering a wide variety of topics, from math concepts to protein modeling programs.

Woodridge, Il, Us

• Performed quality assurance tests on products to make sure product was within specifications (quality control).• Tested and modified formulas for new products (research and development).• Reviewed, modified, and created Material Safety Data Sheets for products (regulatory).• Assisted in modification and implementation of new protocol for creating new products and shipping old and new products (regulatory).

Champaign, Il, Us

• Served as a resource to the residents.• Created informative bulletins and planned programs for residents to participate in.

• Provided first aid to staff members and campers

Champaign, Il, Us

• Experimented with isolation and biochemical characterization of M. Smegmatis PyrR (a protein) from the cloned gene pyrR. • Isolated protein using streak plating, ligation, gene cloning, and PCR amplification.• Performed gel electrophoresis to analyze protein.

Champaign, Il, Us

• Investigated effects of small molecules (mainly Riboflavin) on apoptosis, focusing on the apoptosis cascade of a certain cell line.• Maintained cell culture.• Applied varying concentrations of Riboflavin to cells and observed cell viability using cell count as a measurement.

Master Of Science (M.S.), Biomedical Engineering

B.S., Integrative Biology