Coordinator | Clinical Research
at Interior Health Authority
Penticton, BC, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 03 Mar, 2026 | Not Specified | 04 Nov, 2023 | 2 year(s) or above | Clinical Research Associates,Research,Clinical Practices,Protection,Remote Data Capture,Powerpoint,Rdc,Ccra,Completion,Excel,Training,Email,Interpersonal Skills,Databases,Health Research,Clinical Trials | 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:
Interior Health has a Term-specific Full-time Coordinator, Clinical Research opportunity available at Penticton Regional Hospital. The end date of this position is approximately March 2026.
EDUCATION, TRAINING AND EXPERIENCE
- A level of education, training, and experience equivalent to a Master’s degree in a health research, healthcare, or clinical research discipline or equivalent experience.
- A minimum of five years of practical clinical research work experience at a research site. Other clinical research environments will be considered. A minimum of five years of practical clinical research work experience at a research site may be considered in lieu of education.
- Certification through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) as a Certified Clinical Research Coordinator (CCRC), a Certified Clinical Research Associate (CCRA), or a Certified Clinical Research Professional (CCRP) is strongly preferred. Certification is required within two years of hire date.
- Completion of Tri-Council Policy Statement 2: Ethical Conduct for Research Involving Humans and GCP requirements for protection of the rights of study participants training.
SKILLS AND ABILITIES
- In-depth knowledge of Health Canada Food and Drug Act, Division 5, Part C; International Committee on Harmonization Part E6 – Good Clinical Practices; and US Food and Drug Act regulations 21 CFR and 45 CFR part 46 pertaining to clinical trials.
- Functional understanding of the Freedom of Information and Privacy Act (FIPPA), in particular section 35.
- Excellent interpersonal skills, advanced written and verbal communication, pro-active problem-solving abilities, and a well-demonstrated ability to work with others as part of an interdisciplinary team.
- Exceptional attention to detail and an advanced ability to organize information and multi-task/ prioritize in a busy environment.
- Highly proficient with databases, MS Office (particularly Word, Excel, and PowerPoint), email, and the internet.
- Experience with Remote Data Capture (RDC) and Electronic Data Capture (EDC) systems.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Penticton, BC, Canada