Jack Kerrigan Email & Phone Number

London, Gb

London, England, United Kingdom

In September 2023, I re-located to London to work solely within the IQVIA/Roche UK Model.

County Dublin, Ireland

In addition to my CRA 1 roles and responsibilities mentioned below, as a CRA 2 I am involved in more trials of a complex nature with a higher number of sites under my care. I also provide internal training and guidance to new CRA's in IQVIA and the Roche Pharmaceuticals Clinical Research Model. One way of doing this is through Observational Site Visits, where new CRAs can accompany me on a site visit for real world learning and practical experience. As part of this role I will also be assigned a Buddy within IQVIA to be a friendly face and mentor to a new CRA during their first year or so in the company (and thereafter).

County Dublin, Ireland

My role and responsibilities involved:Participation in the investigator recruitment process, performing site evaluation visits of potential investigator's sites to evaluate the capability of the site to successfully manage and conduct the clinical study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provide training on completion of the eCRF and EDC system, monitoring activities and study close-out activities.Assist in resolving any issues to ensure compliance with site file audits and/or inspections.Assure adherence to Good Clinical Practice, Good Pharmacovigilance Practices, Investigator integrity, and compliance with all study procedures through on-site monitoring visits. Perform validation of source documentation as required by sponsor. Prepare monitoring reports and letters per the timelines defined in IQVIA and Roche Pharmaceuticals SOPs.Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Perform investigational product inventory.Review the quality and integrity of the clinical data through (1) remote review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.Serve as primary contact between IQVIA, Sponsor and Investigator; coordinate all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.Ensure all study deliverables are completed per IQVIA and study timelines. Perform site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation. Establishing regular lines of communication and administering protocol and related study training to assigned sites. Escalating quality issues as appropriate. Managing progress by tracking recruitment, case report form (CRF) completion, and data query resolution

Dundrum, County Dublin, Ireland

My role required effective communication skills while handling a high volume of medical information, with a strong emphasis on attention to detail, daily deadlines, activity tracking, teaching/quality control of work, client services/relationships, and adherence to industry regulations and protocols. I worked closely with an internationally based team to fulfill my role which involved:- Processing large quantities of insurance claims and drafting letters on behalf of our clients (medical professionals), while meeting daily and weekly targets, and addressing a wide variety of client, patient and hospital queries related to medical billing via phone and email. - I was required to communicate clearly in my writing to insurance companies to justify inpatient stays in hospital, requiring an astute knowledge of many medical conditions, procedures as well as pharmacological treatments/medications.- The strictest standards of client confidentiality in accordance with GDPR regulations were essential in this role.- I engaged with management regularly to troubleshoot issues and resolve any recurring factors effecting team efficiency. I was also responsible for upskilling fellow team members and quality control of their work.- I presented at team meetings every fortnight to provide updates and new information regarding any changes to industry regulations or protocols in my field of work. - I liaised and collaborated with multiple teams in the company to bring multifaceted projects/accounts to completion.

Monkstown, Co. Dublin

My responsibilities included the making and service of coffee and drinks, stock taking and ordering new stock, while performing regular health and safety checks of my work area. I was responsible for recording and maintaining fridge temperatures and a clean work surface throughout the day.I also provided customer service by taking bookings or enquiries over the phone. I also served and waited tables at large events and on very busy weekends, with many staff and customers present.

Dublin, Ireland

Twelve-week placement (June-August 2018) with the ESB working on a major transformation project in the Irish energy industry with a billion-euro capital spend. Working closely with Ernst & Young, I led the development and delivery of a ‘Case for Change’ video to communicate the Business Case for the project to an internal audience of c. 3,000 people. I supported the development of an online Change Management Portal to up-skill business leadership on effective change management practices. I researched and developed key templates and adapted training materials for use on the portal. I was responsible for updating the weekly Project Dashboard which outlined the progress and important upcoming events of the project for the attention of the staff. I also contributed to the organisation of several high level design workshops.

Online Course, Clinical Research Associate Training

Ba In Science, Physiology (2015-2019), I - First Class Honours (70%)

Activities and Societies: Volunteer with the Simon Community Hope Project in Dublin to help raise awareness and money for the Homeless.

Junior And Leaving Certificate, Higher Level

- Elected Prefect by peers & staff 2013/14 - Habitat for Humanity, Charity Volunteer Work (March 2013) in Andola Zambia, successfully.