Labcorp Drug Development: Junior Clinical Research Bardi

Labcorp Drug Development: Junior Clinical Research
Bardi
Emilia Romagna, Bardi

Job Overview:

Covance FSP are looking to hire a CRA based preferably in MILAN OR ROME but we can consider also other well connected locationsIn this position you will be fully dedicated to our sponsor and will be home based. This is an unblinded CRA position to perform Pharmacy site visits.

At Covance, you can redefine what is possible and discover your extraordinary potential within ourFunctional Service Providerteam (FSP). As a Covance employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor.

Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Covance has an FSP opportunity to match your area of expertise. Each FSP offers a unique opportunity to be a part of the drug development cycle and see a product through to launch.

We have multiple partnerships giving you the variety and the flexibility to stay with sponsors, try a new external secondment or work in house on Covance studies. With the support of exceptional peopleand an energized purpose, you'll be empowered to own your career journey with dedicated mentoring, training and personalized development planning. Responsibilitiesinclude:

All details of site management as prescribed in the project plansRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasksNegotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreementsSerious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs. Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systemsEducation/Qualifications:

University degree in life sciences (preferrably in pharmacy), or certification in a related allied health profession from an appropriately accredited institution (e. G. , nursing licensure)CRA certification and some clinical trials experienceExperience:

Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH GuidelinesExcellent understanding of Serious Adverse Event (SAE) reportingAbility to resolve project-related problems and prioritize workload for self and teamREMOTE HOME BASED