Clinical Recruiting Coordinator
at BIOPHARMA SERVICES INC
Toronto, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 Nov, 2024 | Not Specified | 29 Aug, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
- Maintain up-to-date knowledge of study information and study planning strategies
- Assist Manager/Director to maintain up-to-date knowledge of competition and industry trends
- Collaborate with Manager/ Director in the development of recruitment strategies for various segments of the population and ensure that an adequate number of suitable volunteers are recruited for all studies
- Conduct regular communication of goals, priorities and studies with Clinical Contact Centre Representatives to keep staff informed of daily objectives and study enrolment status
- Changes from scheduled timelines or recruitment challenges are communicated in a timely manner to mitigate risks associated with study enrolment
- Manage the tasks of the Clinical Contact Centre Representatives including acknowledgment of Study Briefings, updating the clinical database, responding to inbound calls and booking appointments
- Organize, oversee and conduct clinical staff training
- Assist Manager/Director to do performance reviews and coaching
- Write, Revise, and approve SOPs and internal procedures
- Participates in protocol review and development
- Enter and/or update potential volunteer information in the Recruitment Database
- Preparation of Study Master List
- Generate recruitment highlights (protocol summary)
- Informing potential subjects of their medical screening results
- Ensures that the volunteer’s study participation history; washout and lockout dates as per Clinical RSVP (cRSVP) are verified and cleared prior to study admission.
- Assigning tentative subject numbers
- Offer study participation and provide tentative study information to potential study volunteers
- Administer telephone questionnaires to potential study volunteers
- Look, reschedule and/or cancel medical screening appointment(s) for potential study volunteer(s).
- Populates the study-specific details into CDMS (including all pertinent details including but not limited to the study drug/ study demographics/ stipends/ referral fees/ screening allocations/ study-specific inclusion & exclusions etc…)
- Build and maintain solid relationship with study volunteers by providing excellent customer service
- Resolve any volunteer related issues in a professional and timely manner
- Provide metrics on advertisement, performance and recruitment activities
- Provide statistical reports to management e.g. month end report, study recruiting stats
- Participate in departmental meetings and assist management in implementing outlined departmental initiatives and developing strategies to maintain and increase subject retention
- Perform any other duties as required permissible by training and experience
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
Toronto, ON, Canada