Laura Lassouw-Polman Email & Phone Number

Sairopa develops novel treatments for cancer by modulating the patient’s immune system. In 2021, Sairopa acquired a portfolio of therapeutic antibodies and initiated clinical testing of two of its lead compounds in Phase 1 clinical trials in 2022.

Oss, Nl

Director for a proof of concept Early Research & Development study in CLL Director on Early Oncology NSCLC pre clinical - FTIH study

Oss, Nl

Associate Director/International Sr Study Leader/ , for FTIH BC studyAssociate Director/International Sr Study Leader/ , for a proof of concept Early Research & Development study in CLL#acalabrutinib #FDA International Sr Clinical Trial Manager for a Ph 1b/2 study in subjects with Waldenstrom Macroglobulinemia , supported FDA filingBudget holder, vendor oversight, Study Management Team lead, owner of timelines, project planning, deliver quality, teamwork, NDA filing, CSRs, Phase I & Phase II, international teams, international approach, follow the science, oncology, drive, passion, make it happen!

Dublin, Ie

Responsibilities in my work include identification, selection, initiation, and close-out of appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP. Involvement, when required, in other areas of study management and staff training. Coaching and mentoring of monitoring competence to inexperienced/less experienced colleagues. Contribute to the culture of process improvement with a focus on streamlining business processes adding value to business and meeting client needs. Independently and proactively coordinate the necessary activities required to set up and monitor a study.

Paris-Saclay, Île-De-France, Fr

Clinical Study Management, Baby Nutrition

Internal review and set up of Company Procedures, SOPs, Work instructions & CRA assessment.

Senior Clinical Trial Associate, acting project manager, Global Clinical Trial Management at MSD. As a Sr CTA part of the global study management team for managing globally initiated clinical studies. Responsible in cooperation with Project Manager for managing the clinical trial in a timely, effective and efficient manner.Currently working on the start up of an international trial with 17 participating countries.

Wilmington, Nc, Us

Senior Clinical Research Associate, NL representative for international studies with participating sites in the Netherlands. Responsible for site management, local project management, recruitment, review of the trial at site, maintaining site contact in discussion with participating investigator and study team, monitoring the project on national basis and team work within the international study team.

Wilmington, Nc, Us

Senior Clinical Contract Specialist, position within Study Start Up Team, negotiation on contract and budgets for participating sites in the Netherlands, including but not limited to hospital-, pharmacy, -laboratoy-, radiology contracts.