20 beste Stellen als clinical project management in zürich, zh – aktuell auf Personalsuche

Clinical Trial Liaison
Kiniksa Pharmaceuticals —Zug, ZG
- Englisch
- Microsoft Office
- Projektmanagement
Direkt bewerben
Clinical Education Specialist_Community and Engagement
Nobel Biocare —Kloten, ZH
- CHF 84’600 - CHF 131’200 pro Jahr
- Management-Erfahrung
- Englisch
- Projektmanagement
- Bezahlte Feiertage
- Bezahlte Ferien
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Zürich, ZH
- 100%
- Homeoffice
- Management-Erfahrung
- Doktorat
- Schreibfähigkeiten
System Integration & Testing Project Lead
Roche —Zug, ZG
- 100%
- Englisch
- Bachelor
- Führungserfahrung
Strategy and Transformation Consultant - Life Science
Capgemini Sogeti —Zürich, ZH
- Microsoft Powerpoint
- Microsoft Excel
- Doktorat
- Empfehlungsprogramm
CRA Switzerland
サイネオス・ヘルス —Zürich, ZH
- Homeoffice
- Englisch
- Bachelor
- PC-Kenntnisse
Associate Program Director, Dravet
Biogen —Baar, ZG
- 100%
- Analysefähigkeit
- Projektmanagement
- Führungserfahrung
Regulatory and Start Up Specialist - Switzerland
IQVIA —Zug, ZG
- 100%
- Homeoffice
- Bachelor
- Homeoffice-Möglichkeit
1 Tag
Prinicipal - Industry Advisory
Genpact Onsite Services - Switzerland Branch —Zug, ZG
- 100%
- PMP
- Englisch
- Master
Direkt bewerben
Internship Clinical Study - Hospital of Lucerne (m/w/d) 100%
greenteg AG —Rümlang, ZH
- 100%
- Hybrides Arbeiten
- Englisch
- Forschungserfahrung
- Bachelor
Direkt bewerben
7 Tage
Global Medical Director, Evidence Generation Lead
Biogen —Baar, ZG
- 100%
- Microsoft Excel
- Doktorat
- Forschungserfahrung
Director, Statistical Programming
CSL Behring —Glattbrugg, ZH
- CHF 239’000 - CHF 308’000 pro Jahr
- 100%
- Management-Erfahrung
- Wartung
- Englisch
EU CTR Submission Lead
Biogen —Baar, ZG
- 100%
- Master
- Analysefähigkeit
- Bachelor
Sr Director, Country & Site Operations (CSO)
Biogen —Baar, ZG
- 100%
- Management-Erfahrung
- Projektmanagement
- Bachelor
Associate Director EU CTR Strategy & Operations Excellence Lead
Biogen —Baar, ZG
- 100%
- Projektmanagement
- Führungserfahrung
Site Start-Up Specialist based in Switzerland
Fortrea —Zürich, ZH
- 100%
- Homeoffice
- Microsoft Office
- Bachelor
- Kommunikationsfähigkeit
1 Tag
Buyer
HAI4M —Zürich, ZH
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Global Category Manager - CRO (Director)
Takeda Pharmaceutical —Zürich, ZH
- CHF 177’400 - CHF 243’980 pro Jahr
- 100%
- Management-Erfahrung
- Master
- Analysefähigkeit
7 Tage
Director of Intellectual Property
CSL Behring —Glattbrugg, ZH
- 100%
- Management-Erfahrung
- Doktorat
- Forschungserfahrung
2 Tage
Strategic Buyer Hocoma
HAI4M —Zürich, ZH
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel

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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.

Direkt bewerben

Erweiterte Suche

clinical project management Jobs in zürich, zh

Clinical Trial Liaison

Clinical Education Specialist_Community and Engagement

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

System Integration & Testing Project Lead

Strategy and Transformation Consultant - Life Science

CRA Switzerland

Associate Program Director, Dravet

Regulatory and Start Up Specialist - Switzerland

Prinicipal - Industry Advisory

Internship Clinical Study - Hospital of Lucerne (m/w/d) 100%

Global Medical Director, Evidence Generation Lead

Director, Statistical Programming

EU CTR Submission Lead

Sr Director, Country & Site Operations (CSO)

Associate Director EU CTR Strategy & Operations Excellence Lead

Site Start-Up Specialist based in Switzerland

Buyer

Global Category Manager - CRO (Director)

Director of Intellectual Property

Strategic Buyer Hocoma

Ich möchte aktuelle Job-E-Mails für Stellen als clinical project management in zürich, zh erhalten

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