McKesson
McKesson

McKesson ir veselības aprūpes uzņēmums, kas darbojas farmaceitisko produktu izplatīšanas, medicīnas preču un veselības aprūpes pakalpojumu jomā. Tā darbība palīdz aptiekām, klīnikām, veselības aprūpes sistēmām un pacientiem saņemt nepieciešamo terapiju, vienlaikus atbalstot efektīvāku veselības aprūpes darbību un noturīgu reaģēšanu uz zāļu trūkumu.

Uzņēmums izstrādā arī aptieku pārvaldības programmatūru un piedāvā konsultāciju un tehnoloģiju risinājumus specializētām praksēm. McKesson sadarbojas ar biofarmācijas organizācijām un atbalsta onkoloģijas un biofarmācijas prakses, nodrošinot pakalpojumus, kas vērsti uz medikamentu pieejamību, ārstēšanās ievērošanu, komercializāciju, uz datiem balstītām atziņām un reālās pasaules pierādījumiem.

Regulatory Affairs Coordinator – Tennessee Remote

Coordinate FDA and Good Clinical Practice documentation for SCRI’s community oncology trials. Support clinical sites and sponsors with regulatory records, signatures, audits, and compliance.

Apraksts

  • Coordinate regulatory compliance for industry sponsors and network sites.
  • Partner with regulatory leaders, department directors, and principal investigators to support compliance.
  • Prepare for audits and meet strict deadlines.
  • Process regulatory document signature requests using an electronic signature platform.
  • Track regulatory documents awaiting site signatures.
  • Support Clinical Operations sites and internal managers with site-level regulatory needs.
  • Set up and maintain regulatory document systems for paper and electronic records.
  • Maintain FDA- and GCP-required records for sites, studies, sponsors, and networks.
  • Check regulatory documents against local SOP requirements for format and content.
  • Keep physician credentials and other key records current.
  • Assess site requests for regulatory support and direct each issue to the appropriate resolution process.

Prasības

  • Associate degree required; bachelor’s degree preferred.
  • Regulatory experience preferred.
  • Customer service experience preferred.
  • Knowledge of FDA and Good Clinical Practice (GCP) regulatory documentation.
  • Ability to ensure regulatory documents meet local standard operating procedure (SOP) requirements.
  • Ability to meet strict deadlines and prepare for audits.
  • Ability to keep physician credentials and other critical compliance records current.

Priekšrocības

  • Benefits package supporting physical, mental, and financial well-being.
  • Competitive compensation package.
  • Annual bonus or long-term incentives may be offered.
  • Equity may be included in compensation.
  • Total Rewards package.

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