Alejandro Lahire

I am currently working as a Clinical Study Coordinator at Vall d'Hebron Hospital (VHIO), but the time has come for a change - I am actively looking for an opportunity to start my career as a Clinical Research Associate (CRA).

My areas of expertise are: Onco-Hematology (lymphoma, transplants and CarT-Cells) and solid tumors (thoracic and head/neck), both phase I and phase II/III. At the present time I have +5 years of experience in the field of clinical trials.

WHAT MAKES ME A SOLID CANDIDATE TO JOIN YOUR TEAM?

• great teamwok spirit
• deep empathy, which drives me to have a conciliatory and conflict-resolving personality
• fearless of changes, especially if they involve new learning
• always willing to take on new challenges
• strong communication skills
• insightful, with a sense of intuition that helps me identify potential problems even before they arise
• practical and straightforward, high ability to find effective solutions 
• acute attention to detail
• efficient time and resource management skills
• absolute willingness to mentoring; I take great pride in sharing my knowledge and seeing how my fellows grow and progress

Clinical Study Coordinator at VHIO from March 2021 to present

• Study set-up, from the initiation visit to the closing visit.
• Management of the cross-sectional teams participating in the study
• Weekly meetings with investigators
• ISF maintenance and administrative tasks
• Review of monitoring letters and discussion of deviations
• Preparation of audits and inspections
• Scheduling patient visits and protocol assessments, resolution of study-related doubts

• Data entry in the eCRF
• Query resolution
• Preparation of on-site and remote monitoring visits
• Preparation of audits and inspections
• Data Manager’s team leader from 2019-2021: organize the work and the time dedicated to the different tasks, help the team to meet both personal and team objectives, regular meetings with our manager and investigators to define strategies and circuitsç

• On-site monitoring, remote monitoring, and site management activities
• Preparation of close-out visits
• Source data verification and Informed Consent process verification
• Investigational product accountability, inventory, and reconciliation
• Updating and maintenance of the eTMF
• Confirmation and follow-up letter writing, monitoring report writing
• Protocol deviation notice, reporting and retraining of the staff if necessary

• Degree in Biomedical Sciences, University of Barcelona (September 2011 - September 2015)
• Master’s Degree in Genetics/Genomics, University of Barcelona (September 2015 - September 2016)
• Master’s Degree in Clinical Trials, ESAME Pharmaceutical Business School (October 2017 - June 2018)