/ L'annuaire des offres d'emploi en Suisse
FR DE
Back to job offers

Biospecimen Specialist

Proclinical Lucerne 20.09.2026 Déposer ma candidature
Company
Proclinical
Location
Lucerne
Date
20.09.2026
Reference
354375

Keep the heartbeat of innovation running

Join a dynamic team focused on biospecimen acquisition and management to ensure cutting-edge pharma never misses a beat. In this role, you will oversee the Employee Specimen Donation Program (ESDP), manage biorepository activities, and ensure compliance with regulatory standards. This position requires a detail-oriented, self-motivated individual who can work autonomously while collaborating effectively with internal and external stakeholders. To be considered for this role, you must have the right to work in this location or hold an EU passport.

Responsibilities

  • Lead and execute the Employee Specimen Donation Program, including designing promotional campaigns to drive engagement.
  • Manage biorepository activities such as biological material processing, registration, shipment, inventory searches, and sample kit creation.
  • Oversee end-to-end project management to fulfill customer specimen requests.
  • Collaborate with permitting agencies and compliance teams to meet import/export and safety requirements.
  • Conduct data management tasks, including data review, quality checks, discrepancy resolution, and database entry in validated systems.
  • Maintain accurate documentation of sample collection and study information in line with established procedures.
  • Ensure compliance with legal, regulatory, and ethical standards, including informed consent and data privacy regulations.
  • Interface with diverse stakeholders to establish timelines and achieve project goals.

Key Skills and Requirements

  • Bachelor's or Master's degree in Life Sciences or equivalent experience in sample acquisition, biobanking, or related fields.
  • Hands-on experience handling biological specimens, with a willingness to work with potentially infectious materials.
  • Knowledge of ethics and compliance, including informed consent, IRB protocols, and data privacy regulations (e.g., GDPR).
  • Proficiency in Microsoft Office, Google Suite, and validated systems like LIMS.
  • Strong attention to detail, organizational skills, and commitment to high-quality deliverables.
  • Excellent interpersonal, verbal, and written communication skills.
  • Ability to lift up to 10-15 kg.
  • English proficiency (minimum B2 level).
  • Experience in research, diagnostics, pharmaceutical, CRO, or medical device industries.
  • German language skills are an advantage.

Déposer ma candidature

Accepted formats: PDF, Word, RTF or ODT. Maximum size: 3 MB.