Aktiviere Job-Benachrichtigungen per E-Mail!

Clinical Development Lead Oncology

Talentify

Rotkreuz

Vor Ort

CHF 110’000 - 150’000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Erstelle in nur wenigen Minuten einen maßgeschneiderten Lebenslauf

Überzeuge Recruiter und verdiene mehr Geld. Mehr erfahren

Starte ganz am Anfang oder importiere einen vorhandenen Lebenslauf

Zusammenfassung

An innovative diagnostics company is seeking a Clinical Development Lead in Oncology to drive clinical programs focusing on Chronic Liver Diseases. The ideal candidate should have a PhD or equivalent in Life Sciences, with at least 3 years of relevant experience and a robust understanding of clinical standards. Responsibilities include leading study designs, collaborating cross-functionally, and providing regulatory expertise. Opportunity for significant contribution to personalized healthcare in liver fibrosis, with a competitive salary package.

Qualifikationen

  • Advanced degree in Life Sciences (PhD, PharmD, or equivalent) or a Medical degree.
  • Minimum of 3 years’ experience in academia or industry.
  • Proven ability to lead clinical development programs.

Aufgaben

  • Lead clinical development activities for diagnostic solutions.
  • Guide clinical study design and evidence generation strategies.
  • Collaborate with cross-functional teams to implement clinical strategies.

Kenntnisse

Leadership
Communication
Analytical Thinking

Ausbildung

PhD or PharmD in Life Sciences

Jobbeschreibung

We are looking for aClinical Development Lead – Oncologyto spearhead clinical development activities for innovative diagnostic solutions inChronic Liver Diseases, with a particular focus onpersonalized healthcare in Liver Fibrosis. This role involves leading clinical programs in collaboration with an external pharmaceutical partner, contributing to the development of high-impact medical diagnostics.

Responsibilities

  • Serve as asubject matter expertin Liver Fibrosis and Oncology, guiding clinical study design and evidence generation strategies.
  • Lead thedesign, execution, and interpretationof clinical studies, including protocol development and report writing to support product development.
  • Collaborate with cross-functional teams includingMedical Affairs, Clinical Operations, Regulatory Affairs, Biometrics, Development, and Qualityto ensure effective implementation of clinical strategies.
  • Build and maintain strong relationships with internal stakeholders and external partners to align on business goals and ensure operational excellence.
  • Represent Clinical Development in cross-functional initiatives, supportingclinical utility, intended use, and claim extensionsfor diagnostic products.
  • Providescientific and regulatory expertisein IVD product development, including contributions to regulatory submissions and responses to health authorities.
  • Conduct and overseecomprehensive literature reviews, synthesize scientific data, and create original scientific content.
  • Demonstrateleadership and mentoringcapabilities, fostering a collaborative and growth-oriented team environment.

Must-Haves

  • Advanced degree in Life Sciences (PhD, PharmD, or equivalent) or a Medical degree with relevant experience in the healthcare industry or academia.
  • Minimum of3 years’ experiencein academia, diagnostics, or the pharmaceutical industry, ideally with exposure to IVD or medical device development.
  • Proven ability to lead clinical development programs, with solid knowledge ofclinical standards and regulations(e.g., ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA).
  • Strong understanding of the healthcare ecosystem and experience working inmatrixed, cross-functional teams.
  • Agile mindset and alignment withVACC leadership principles(Visionary, Architect, Coach, Catalyst).
  • Excellent communication, presentation, and negotiation skills influent English.
  • High adaptability and analytical thinking, with the ability to work independently in a fast-paced environment.
  • Willingness to travel up to10–15%, depending on project needs.

Duration: 12 months

Start date: ASAP

If you want to learn more about this opportunity please feel free to reach out directly to mbertrand@actalentservices.com.

*While we appreciate every application, please note that due to the high volume of responses, we may only be able to contact shortlisted candidates.

Job Title: Clinical Development Lead Oncology

Location: Rotkreuz, Switzerland

Job Type: Contract

Aerotek, an Allegis Group company. Allegis Group AG, Aeschengraben 20, CH-4051 Basel, Switzerland. Registration No. CHE-101.865.121. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice available at https://www.allegisgroup.com/en-gb/privacy-notices.

To access our Online Privacy Notice, which explains what information we may collect, use, share, and store about you, and describes your rights and choices about this, please go to https://www.allegisgroup.com/en-gb/privacy-notices.

We are part of a global network of companies and as a result, the personal data you provide will be shared within Allegis Group and transferred and processed outside the UK, Switzerland and European Economic Area subject to the protections described in the Allegis Group Online Privacy Notice. We store personal data in the UK, EEA, Switzerland and the USA. If you would like to exercise your privacy rights, please visit the "Contacting Us" section of our Online Privacy Notice at https://www.allegisgroup.com/en-gb/privacy-notices for details on how to contact us. To protect your privacy and security, we may take steps to verify your identity, such as a password and user ID if there is an account associated with your request, or identifying information such as your address or date of birth, before proceeding with your request. If you are resident in the UK, EEA or Switzerland, we will process any access request you make in accordance with our commitments under the UK Data Protection Act, EU-U.S. Privacy Shield or the Swiss-U.S. Privacy Shield

Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.
eine PDF-, DOC-, DOCX-, ODT- oder PAGES-Datei bis zu 5 MB per Drag & Drop ablegen.