Position: Associate

Job type: Full-time

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Job Overview

Senior Clinical Research Associate II ( sCRA II ) - Switzerland

Location: Zurich, Switzerland / Home Office, Switzerland

A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 70,000 employees advance life-changing medicines across a wide range of therapeutic areas.

In this role, you will work with our renowned key sponsors and advance the development of innovative, life-changing medications for a variety of therapies. If you are looking to broaden your therapeutic expertise whilst gaining exposure within a world-class pharmaceutical working environment, this is an excellent opportunity!

What We Have To Offer
  • work as part of a diverse and stable team
  • in-depth onboarding, including personal support from your mentor
  • flexible working hours and compensatory time off in lieu
  • a 100% home-based, permanent employment contract
  • travel time = work time
  • highly competitive compensation packages
  • regular, merit-based salary adjustments
  • significant employer contributions to an attractive pension scheme
  • excellent training and career development opportunities
  • strong support from Line Management and more than 20’000 colleagues worldwide
  • the world’s most renowned pharmaceutical companies as our satisfied, repeat customers for many years
Your Responsibilities
  • Own all aspects of site management as described in the project plans
  • Ensure the study staff conducting the protocol receive all materials and instructions to safely enter patients into the study
  • Protect study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible entries
  • Perform the required monitoring tasks in an efficient manner, according to SOPs and established guidelines; prepare accurate and timely trip reports
  • Review progress of projects and initiate appropriate actions to achieve target objectives
  • Interact with internal work groups to evaluate needs, resources and timelines
  • Act as contact for clinical trial suppliers and other vendors as assigned
  • Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Independently perform CRF reviews
  • Generate queries and resolve issues according to data review guidelines on Labcorp or sponsor data management systems
Education/Qualifications
  • Degree in a relevant field such as life sciences, pharmacology, biology, chemistry, health care, health management, (veterinary) medicine, nursing, etc.
  • In lieu of the above, a completed vocational education or professional experience (e.g. as study nurse, study coordinator) in a relevant field
  • Valid driver’s license
Experience
  • Profound professional experience in a related function as senior / lead CRA, with a focus on independent site monitoring in Switzerland
  • In-depth familiarity with applicable Swiss and international regulatory requirements such as ICH / GCP
  • Computer literacy in Microsoft Office (Word, Excel, PowerPoint) and preferably in relevant software solutions for clinical trials, e.g. eTMF (e.g. Veeva Vault)
  • Effective time management and organizational skills and a keen attention to detail
  • Ability to establish and maintain effective, trustful working relationships with internal and external stakeholders
  • Excellent communication skills in business fluent German and English – both spoken and written – are a must; French language skills a plus
Remote

2021-73539

Covance is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
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Deadline: 04-05-2024

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