Katie Proctor Email & Phone Number

Warsaw, Mazowieckie, Pl

Zug, Ch

Zug, Ch

Vendor Management Specialist with a broad range of responsibilities including third party vendor identification, assessment, performance and relationship management. The role required establishing a strong and collaborative working environment with key vendors to effectively manage their performance and to continually optimise and streamline processes across the clinical trials conducted within the company. Organised, prepared and led vendor governance meetings, assessing service delivery via analysis of Key Performance Indicators (KPIs), taking ownership of issues escalated by project teams and clients, and managing appropriate action plans to ensure a successful resolution and a win-win scenario for all parties.Acted as a trusted advisor providing support to internal project teams, departmental heads and company divisions on vendor management-related activities, promoting good practices and identifying opportunities for efficiencies and improvement.

Zug, Ch

Project Manager responsible for the management and oversight of all aspects of large, Phase II and III international clinical trials to ensure project deliverables were met on time and on budget, whilst maintaining high quality. The role involved building and maintaining effective client relationships, set up and management of vendors, finance management and authoring of study documents and plans.Provided leadership, training and coaching to the cross-functional study teams; defined training requirements, communicated important study messages during team meetings, developed tools to support compliance and led productive face-to-face CRA training sessions.

Oxford, England, Gb

A Clinical Programme Manager responsible for the clinical development of novel immunotherapies for three separate allergy programmes, comprising phase IIa, IIb and IIIb trials. The role involved the project management of all clinical aspects of Circassia’s outsourced trials to ensure successful completion of trials on time and within budget, via the management of third party suppliers. Accountable for many aspects of project development, e.g. took lead responsibility for the generation of protocols, consent forms, requests for proposals, clinical study reports, SOPs and other study and regulatory documents, the selection of vendors and negotiation of budgets, and the review and analysis of clinical data.

Burnaby, Bc, Ca

A broad and creative role overseeing Phase I and II clinical trials in Canada and the US, including Xenon’s most advanced analgesic programme. Gained a deep understanding and hands on experience of designing, planning and conducting trials in the rare disease environment, addressing the challenges associated with orphan drug development, such as identifying and recruiting for patients and designing small clinical trials. Gained experience of the US and European regulatory aspects of orphan drug development.Participated in the development of Xenon’s clinical strategy, which included researching and proposing future indications and designing clinical trials. Provided leadership and oversight for the day-to-day execution of activities related to trial conduct and managed all vendors/service providers involved in the trials.

Burnaby, Bc, Ca

Bagsværd, Dk

Regionally based CRA on a global, observational Phase IV clinical study in diabetes in the primary health care.Gained hands on experience of site monitoring and management. Had extensive contact with external clients (Health Care Professionals) and was accountable for identifying, recruiting, training and managing new study sites, in addition to performing SDV and making follow-up motivational visits.

New York, New York, Us

Independently sought an internal secondment within Clinical Research Operations, following trials across multiple therapeutic areas. Gained an awareness and understanding of the set up, conduct and close out of trials, and gained hands on experience of site monitoring and management. Undertook a variety of training courses, including ICH GCP.

New York, New York, Us

A Synthetic Research Chemist in Drug Discovery, working on infectious disease programmes and receiving 2 Individual Performance Awards for outstanding project contributions.

New York, New York, Us

Undertook an internal secondment to develop new skills in the analytical chemistry field. Upon completion of the secondment, initiated and became the primary point of contact for 200 chemists, providing advice and guidance through sharing knowledge and experience.

1St Class Mchem (Masters) Biological Chemistry, With 1 Year In Usa, Chemistry

3Rd Year Of Mchem Degree