Clinical Trial Assistant
IQVIA
Moscow, Russia
4 дня назад

Are you passionate about working on innovative programmes in oncology, rare disease, cardiovascular, and other therapeutic areas within world-renowned top 5 pharma & biotech?

Great, because we're hiring!

We're looking for innovative clinical research professionals just like you to join our global clinical operations teams across Europe, specifically in RUSSIA, MOSCOW

We are hiring Clinical Trial Associates (CTA) :

CTA I : Up to 2 years’ experience in global clinical trials.

CTA II : Minimum 2 years’ experience in global clinical trials. Roles that map to the CTA II category would include : Business Analyst, Finance Coordinator, Regulatory Associate

CTA III : Minimum 4 years’ experience in global clinical trials. Roles that map to the CTA III category would include : Contract Specialist, Study Start Up Specialist

As CTA I you will be involved in the following activities but not limited to, setting up and maintaining applicable TMF (both electronic and hard copy versions).

  • Alert management where current status of data quality or performance is at risk to noncompliance. Maintaining, updating, and inputting information and / or documents into applicable databases for clinical trial and / or data tracking;
  • ensuring reporting system records and quality standards are appropriately maintained.

    You will track incoming and outgoing clinical and regulatory documents / updates for investigator sites, studies, or project team while supporting assigned group(s) or team(s) in preparing applicable study documents.

    You will manage the central inbox and process site requests to appropriate team members and serve as the primary point of contact for field monitoring staff and global DRA.

    As CTA II you will perform all or some of the tasks outlined under the CTA I role, and in addition, may also perform all or some of the following responsibilities :

    Prepare site specific ICF and any other relevant forms according to local SOP. Prepare and compile dossier for initial HA and IRB submission or amendment and oversee associated activities, responses and communications with obtaining approvals for the assigned country(ies).

    Provide support for trial budget and investigator site payments; support the project manager and team with financial tasks.

    Maintain oversight of the entire purchase order process, from set-up to reconciliation, as well as the processing of study invoices.

    CTA III you will perform all or some of the tasks outlined under the CTA I & CTA II role, and in addition, may also perform all or some of the following responsibilities :

    Ensure the successful negotiation and ongoing management of clinical trial agreements with investigative sites and vendor agreements and associated budget management.

    Maintain accurate records, metrics and reports; identify gaps and report to management; make recommendations for process improvement and efficiencies

    IQVIA is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry dedicated to delivering unique and actionable insights.

    Formed through the merger of IMS Health and Quintiles, IQVIA has more than 65,000+ employees worldwide

    At IQVIA, we are committed to advancing human health and delivering real value and outcomes for customers and patients. We view each day as another opportunity to find new solutions and enable the next breakthrough.

    We can offer you :

  • Competitive Salary Packages
  • Excellent Benefits Packages
  • Progression opportunities
  • Employee Referral Scheme
  • Performance Related Bonuses
  • Expert training and guidance
  • Streamlined managerial support
  • Individualised approach to development
  • LI-LT1

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