Position Responsibilities/Duties: Duties will include, but not limited to: Prepare/submit/maintain regulatory documentation for studies; collect study data; coordinate study participant from randomization to treatment; identify study adverse events/side effects; develop/maintain/update study databases, &/or project management tracking systems; administer & provide training on tests/assessments; create/maintain complex research databases; assure safety standards; screen/evaluate candidates for clinical research studies; gather pre-existing health care information; recruit participants & conduct informed consents; Manage implementation/reporting on clinical tests/assessments
Experience & Educational Requirements: The position requires intermediate to advanced professional knowledge of the established principles, practices, procedures, and techniques of clinical, & health sciences research; knowledge of medical terminology/abbreviations; knowledge of clinical trial methods, IRB protocols/requirements, processes for approval, regulatory guideline; knowledge of medical sciences/research concepts/terminology; knowledge/skills in managing clinical research projects/programs; knowledge of research investigatory processes; knowledge of project management principals; knowledge of regulatory policies/guidelines that govern projects, excellent communication skills (written & oral); preferred Bachelor’s degree or 3 years experience.
Job Type: Full-time
Pay: $45,000.00 - $65,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Experience level:
Schedule:
- 8 hour shift
- Monday to Friday
Ability to Commute:
- Albuquerque, NM 87108 (Required)
Ability to Relocate:
- Albuquerque, NM 87108: Relocate before starting work (Required)
Work Location: In person