Clinical Trial Associate

12 Dec 2018
06 Mar 2019
Contract Type

Main Responsibilities

  • Involvement in various tasks to support the Study Team/Management with any trial related activities in all phases of the conduct of the clinical trial;
  • Assist in the preparation of study specific tools (including communication tools such as study specific websites, newsletters, flyers etc.);
  • Support CTM in the set-up and maintenance of study specific trackers to ensure continuous oversight of the study progress;
  • Manage all study-related supplies;
  • Prepare study reports and keep required tools and tracking databases up to date as required;
  • Ensure that clinical trials are conducted in accordance with the protocol, Good Clinical Practice regulations, and internal Standard Operating Procedures;
  • Perform ongoing quality checks/review of documents for the Trial Master File and follow up;
  • Support CTM in preparation and follow-up after site, vendor or sponsor audits and inspections.

Qualifications and Experience:

  • Bachelor's degree in Nursing, Medicine or other Life Sciences or RN degree from an accredited school;
  • Minimum of 2 year experience of clinical trial management (experience as CRA is an advantage);
  • Knowledge of ICH/GCP guidelines (accredited GCP course desirable);
  • Experience in identifying potential deficiencies in the trial progress and assisting in/suggesting corrective and preventive actions (CAPA);
  • Fluency in English (verbal and written) and excellent communication skills;
  • Ability to efficiently organize and prioritize work within a multifaceted framework and set deadlines;
  • Excellent organizational and record-keeping skills with high standards and attention to detail;
  • Flexible, proactive, open-minded and hands-on attitude;
  • Relevant working/residency permit or Swiss/EU-Citizenship required.

Similar jobs

Similar jobs