Clinical Research

WE HAVE EXPERTISE IN THE INDUSTRY

Creating novel pharmaceuticals and cutting-edge medical devices necessitates extensive clinical investigations and an unwavering dedication to upholding scientific rigor, meticulous data administration, and product security.

At Jobby Clinical, our recruitment and comprehensive support services deliver specialized expertise to pharmaceutical and medical device enterprises, contract research firms, academic establishments, and research initiatives funded by federal entities.

clinical research

DISCOVER INDIVIDUALS WHO POSSESS THE APPROPRIATE SKILLS

  • Enlisting Patients, Gaining Consent, and Enrolling
  • Gathering and Reporting Patient Data
  • Initiating and Wrapping Up Study Tasks
  • Dispensing Investigational Drug Therapy to Patients
  • Overseeing Site Activities
  • Managing Trial Projects
  • Managing Trial Database Systems (CTMS, EDC, QMS, TMF)
  • Producing Study Reports and Analyzing Analytics
  • Performing Audits to Ensure Site and Vendor Protocol Adherence, as well as Data Locks
  • Conducting Investigations and Reporting on Corrective and Preventive Actions (CAPA)
  • Creating Case Report Forms (CRF)
  • Crafting Data Management Plans (DMPs) Tailored to Projects
  • Designing, Establishing, and Programming SAS Databases
  • Conducting Data Cleansing Following CDISC Standards (SDTM and ADaM)
  • Development of Protocols, Brochures, and Study Forms
  • Submission of Study Applications and Regulatory Filings
  • Interactions with Regulatory Agencies
  • Management of Trial Master File (TMF)
  • Inquiry into Serious Adverse Events (SAEs)
  • Documentation and Communication of Adverse Incidents
  • Analysis of Human Safety and Protection
  • Application of MedDRA and WHODrug Codes
Clinical Research
Scroll to top