Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $23.00 - $30.00
Work Schedule
Standard Hours
Benefits
Medical insurance
Dental Insurance
Vision Insurance
Employer HSA contribution
Employer-paid life insurance
supplemental benefit offerings
401(k) plan with employer match
generous PTO
Paid holidays
Job Description
AllerVie Health is a pioneering healthcare organization committed to improving the lives of patients suffering from allergies, asthma, and related immunological conditions. Located in Homewood, AL, AllerVie Health is dedicated to providing comprehensive and compassionate care that addresses the complex needs of individuals affected by chronic allergic and respiratory diseases. With a team that includes physicians, clinical professionals, administrative staff, and operational support, the company delivers innovative health solutions aimed at restoring patients' quality of life and vitality. AllerVie Health fosters a dynamic work environment where team members are passionate about their mission, motivated to tackle new challenges, and dedicated... Show More
Job Requirements
- Bachelor's degree in health sciences, nursing, or related field
- at least 1-2 years of clinical research experience preferred
- strong knowledge of GCP, ICH guidelines, and FDA regulations
- ability to stand or sit for extended periods
- ability to move or lift up to 20 lbs
- willingness to perform occasional patient interaction and light clinical tasks
Job Qualifications
- Bachelor's degree in health sciences, nursing, or a related field
- strong understanding of GCP, ICH guidelines, and FDA regulations
- at least 1-2 years of clinical research experience preferred
- phlebotomy experience a plus
- CRC certification (ACRP or SOCRA) preferred or willing to obtain
Job Duties
- Screen, recruit, and obtain informed consent in collaboration with the PI
- meet chart-review, screening, and enrollment targets within defined timelines
- coordinate enrollment, baseline assessments, treatment, and follow-up per protocol
- monitor patient compliance and proactively address conflicts
- schedule and conduct study visits including vital signs, specimen collection, questionnaires/ePRO and document all procedures per GCP
- ensure timely, accurate eSource and EDC entry following ALCOA-C principles
- resolve data queries within protocol-defined timelines
- maintain complete study records including source documents, CRFs, regulatory binders, and the Investigator Site File (ISF) with protocol/version control
- update required technology/sponsor systems on time and ensure continuous data availability for sponsor review
- warehouse/archive data and study documents at study closeout
- conduct all activities in accordance with study protocols, GCP, and regulatory requirements
- monitor patient safety and promptly report adverse events to appropriate parties
- ensure adequacy and readiness of study supplies such as lab kits, investigational products, medical/clinic supplies, and ePRO devices
- manage accountability per study requirements
- prepare for and support interim monitoring visits, audits, and inspections
- complete findings and follow-ups in a timely and thorough manner
- serve as primary contact with sponsors, CROs, monitors, and internal stakeholders regarding site status, visits, queries, and audits
- attend investigator and study start-up meetings
- communicate risks/issues to management well in advance and track to resolution
- collaborate effectively with investigators and cross-functional teams
- assist with training research assistants and support staff
- proactively assist the clinical team with administrative tasks and other job-related duties as assigned
Job Qualifications
Experience
Mid Level (3-7 years)
Job Location
We didn't receive the exact location for this job posting,
please contact the employer.
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