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Clinical Trial Liaison

Kiniksa Pharmaceuticals -
Zug, ZG

Direkt bewerben

Details zur Stelle

Leistungen

Unterkunft

Qualifikationen

Englisch
Microsoft Office
Klinische Erfahrung
Projektmanagement
Bachelor
Kommunikationsfähigkeit
Kranken- & Gesundheitspflege

Vollständige Stellenbeschreibung

The Clinical Trial Liaison (CTL) will be accountable for site engagement, communications and timely patient screening / enrollment of assigned sites for Kiniksa’s applicable studies. The CTL will collaborate closely with the Kiniksa Clinical Operations Team, Clinical Development Lead and Medical Affairs as well as the partner CRO for optimal trial execution.

The ideal candidate will be self-motivated, with prior hands-on experience in executing clinical trials and a natural ability to build and foster productive relationships with clinical site personnel. This role will require significant travel (75%).

The CTL will report to the Associate Director of Clinical Operations overseeing the global site engagement and recruitment strategy for the Clinical Operations department with a dotted line to Regional Clinical Operations Lead of assigned region(s).

Only candidates based in Zug will be considered.

Responsibilities (including, but not limited to):

Be the face of Kiniksa to Investigational Sites taking part in Kiniksa’s applicable studies
Delivering on established KPIs related to patient identification, screening and enrollment targets per site and overall
Developing and fostering relationships directly with clinical site staff and investigators to understand and address challenges in patient enrollment
Developing and maintaining routine communication tools, such as enrollment reports and dashboards, for communicating overall study progress along key metrics, including key risks and challenges, to Senior Management and program team
Supporting development and implementation of site-specific engagement plans for maximizing participation at individual clinical sites
Supporting qualification, site initiation and/or interim monitoring visits with in-person/remote attendance to help amplify and support patient identification efforts
Providing input into and/or developing study related materials to support study participant identification and screening, including support of local clinical site advertising materials
Supporting CRO on feasibility and site selection efforts

Qualifications:

Bachelor’s degree in health or life science; nursing or advanced degree is preferred
A minimum of 5 years’ hands-on clinical trial execution experience, with study coordinator experience highly preferred
Excellent interpersonal and presentation skills, with a natural ability to establish rapport with a wide range of people
Site monitoring and clinical quality compliance experience are strongly preferred
Excellent communication skills, including use of MS Office based software tools for the development and maintenance of effective templates to track, monitor and summarize data and key messages for various audiences
Strong oral and written communication skills in English
Effective project management and risk mitigation skills
Demonstrated ability to successfully enroll clinical studies in a timely manner
Strong organization skills and demonstrated ability to work independently, navigate within a cross-functional matrix environment, and execute tasks with minimal oversight
Ability to travel up to 75% with potential for overnight stays.
Salary is commensurate with experience

Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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