Syneos Health

Sr Clinical Operations Specialist/Feasibility Associate (Denmark or anywhere in EU) - Sponsor-dedicated (BB-CF176)

Found in: Neuvoo DK

Description:

Description

Sr Clinical Operations Specialist/Feasibility Associate 

Sponsor-dedicated

Anywhere in Europe

Syneos Health is looking for split CTA with Feasibility Associate role to one of our big Pharma Client located in Denmark. We could consider candidate based anywhere in Europe.

Main responsibilities:

  • Drive progress, tracking and communication to trial team in the feasibility process in handling and collection of key documents necessary for feasibility assessments
  • Support Global Feasibility Lead in analysis of investigator feedback to ensure an adequate pool of potential investigators that complies with trial timelines and trial key criteria
  • Liaise with Global Feasibility Lead, CRAs and MSLs in creating lists of potential investigators for trials
  • Create and send out Confidentiality Agreements (CDAs) and Site Feasibility Questionnaires to sites including follow up to ensure responses and keep CRAs and MSLs in the loop of the progress
  • Ensure flawless and high-quality communication to external partners (sites)
  • Track and maintain metrics of daily investigator/site contact activities
  • Register new sites and upload documents to ClinicalVault (Veeva)
  • Consolidate investigator information (trial performance, business intelligence, survey results) for Global Feasibility Lead review
  • Ensure compliance in creation of documents and documentation of feasibility process as well as ensuring inspection and audit readiness in the feasibility process
  • Additional assignments as agreed by management for example being driver for using the Trial Management tool
  • Qualifications

  • Associates degree preferred or equivalent
  • Very strong communication and relationship building skills
  • Strong quality mindset and eye for details
  • Conflict management skills
  • Ability to maneuver in a cross functional job including keeping the overview
  • Knowledge of clinical trial conduct
  • Fluent in English (written and spoken)
  • calendar_today1 day ago

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