• Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team.
  • Set up study site for coordination, operation and management.
  • Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning.
  • Clinical Operations
  • Look into business development opportunities
  • Conducted patient assessments and data collection according to study protocols
  • Site management tasks
  • Study coordination tasks
  • Patient recruitment tasks
  • Project management
  • Research Administration
  • Staffing, Staff Management and Training
  • Data Integrity
  • Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files
  • Set up SFRI SMO satellite program development in the region, including business development for the satellite sites.
  • Patient Recruitment/Patient Scheduling and Consenting - Subject recruitment (Hands On), screening, enrollment and scheduling of research participants
  • Set up and implement subject recruitment system- Connect SFRI database, PI data base, field recruitment team, sponsors recruitment resources

Job Details

Functional Area:
Total Positions:
1 Post
Job Shift:
Work from Home
Job Type:
Job Location:
Gender:
No Preference
Age:
26 - 60 Years
Minimum Education:
Masters
Degree Title:
Master in Clinical Research
Career Level:
Experienced Professional
Minimum Experience:
5 Years
Apply Before:
Jun 06, 2025
Posting Date:
May 06, 2025

SF Research Institute Inc.

Healthcare / Hospital / Medical · 1-10 employees -

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