Clinical Studies Technician (6 months) at AliveDx
1262 Eysins, VD, Switzerland -
Full Time


Start Date

Immediate

Expiry Date

20 Jul, 25

Salary

0.0

Posted On

21 Apr, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.

CLINICAL STUDIES TECHNICIAN (6 MONTHS)

We are seeking 2 Clinical Studies Technicians to join our Clinical Affairs Team for a 6-month temporary position in Eysins, Switzerland.

Responsibilities
  • Helping with the planning and management of assigned AliveDx clinical field trials.
  • Support clinical field trial development activities and strategies and assist on the execution of internal testing required for the completion of clinical field trials.
  • Support on material request forms needed for the execution of internal studies.
  • Stock management of investigational and non-investigational products.
  • Responsible of maintaining the sample biobank for clinical studies.
  • Preparation of study binders and clinical study forms required per clinical trial.
  • Assisting on the documentation archiving process and maintenance of electronic Trial Master File (eTMF).
  • Responsible for any function not specifically assigned that leads to the success and growth of AliveDx.
  • Perform any other duties as reasonably requested from the Head of Clinical Affairs to meet the company corporate goals.
  • Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements
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