Senior Clinical Research Associate in Rotkreuz

veröffentlicht
Kontakt
Lucie Nasshan, Basel Professionals Health Care & Life Sciences
Jobtyp
Temporary
jetzt bewerben

job details

veröffentlicht
Ort
Rotkreuz, Zug
Sektor
Life Sciences
Jobtyp
Temporary
Referenznummer
12468
Kontakt
Lucie Nasshan, Basel Professionals Health Care & Life Sciences
Telefon
058 201 55 50
jetzt bewerben

Stellenbeschreibung

Randstad Professionals is currently looking for a Senior Clinical Research Associate who will be assigned an interesting challenge for a major client based in the Central Schweiz.

This contract is an unique opportunity to join a major client, lead player in the IVD industry.

The initial assignment will start in April and will last until December 2019.

Your key responsibilities will include:

  • Responsible for the overall conduct of clinical studies

  • Works independently to complete CRA functions associated with study planning,implementation, monitoring and closing study conduct in accordance with the principles of

  • Good Clinical Practice (GCP)

  • Travels to field sites to independently monitor studies and provide technical assistance, as necessary

  • Ensures collection and maintenance of study documentation (e.g. monitoring plan and reports), legal and regulatory documentation, as applicable

  • Ensures that adverse events, adverse device effects, and incidents occurring during the study are correctly recorded and forwarded within Roche

  • Ensures site compliance with regulations, applicable SOPs, GCP, local regulations and study protocol

  • Acts as first point of contact and provides technical assistance to the sites, as necessary

  • Verifies that source data/documents and other trial documents (e.g. Case report forms,

  • Informed Consents) are accurate, complete and maintained in accordance with data protection regulations

The following skills are required:

  • 3+ years of experience in clinical study coordination, clinical site monitoring

  • Prior experience in diagnostics environment including; IVD-D and Good Clinical Practices (cGCP)

  • A background in biomedical/healthcare services with laboratory experience preferred

  • Bachelor degree in scientific discipline or related field required, or equivalent combination of education

  • Excellent writing and verbal communication skills

  • Excellent English speaking and writing skills, German is a plus

  • Well organized and detail oriented

  • Impeccable record keeping and filing skills

  • Excellent time management skills

  • Ability to work effectively in a cross-functional team at multiple locations in Europe and US

  • Work independently on assigned tasks

  • English: Advanced