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Job Description
Job Summary
With principal investigator oversight, prepares, evaluates and implements research studies to enhance the advancement of clinical practice.
Note: Team Members have 90-days from June 17, 2021 to obtain or recertify if BLS is not current.
Essential Functions
- May serve as primary coordinator / project manager on a variety of research studies with low or moderate regulatory, clinical, and operational complexity; supports the PI and research team members.
- Evaluates and prepares research studies for implementation including: assessment of operational feasibility; budget development; preparation of IRB documents; institutes protocol operations (generation of data collection tools, case report forms); attends study meetings.
- Identifies, recruits, screens, and enrolls eligible subjects per protocol; with appropriate training and delegation, performs protocol-required research activities and/or protocol-required research procedures with low clinical complexity (e.g. six-minute walk test, SF-36, etc.).
- With appropriate training and delegation, monitors patient status; collects, reviews, and documents data into a variety of systems per protocol.
- Maintains research studies in compliance with federal, state, and local law, GCP, contracts, and institutional policies.
- Coordinates and/or performs study activities which may include: identification of adverse events; assist with management of investigational product/test article (drug or device); collection, processing, and shipment of research specimens; and other research activities to the extent permitted by law and policy.
- Communicates, collaborates, networks, and acts as a consultant to the study sponsor and/or CRO, research study centers, academic institutions, investigators, physicians/physician offices, ancillary departments, and the multidisciplinary team (including students and residents).
Qualifications
- Required Bachelor's Degree in health or science related field or equivalent
- 1 year of relevant experience in clinical research and project management Preferred
- CRT-Basic Life Support (BLS) - ARC American Red Cross 90 Days required Or
- CRT-Basic Life Support (BLS) - AHA American Heart Association 90 Days required
Primary Location
SITE - Secchia Center - 15 Michigan St - Grand Rapids
Department Name
Pediatric Research Operations
Employment Type
Full time
Shift
Day (United States of America)
Weekly Scheduled Hours
40
Hours of Work
8 a.m. to 5 p.m.
Days Worked
Monday to Friday
Weekend Frequency
Variable weekends
Spectrum Health requires all team members to receive the COVID-19 vaccinations subject to certain exclusions based on the team member’s job category. Spectrum Health is committed to granting reasonable accommodations in accordance with applicable laws.
Accommodation Notice: If you are a qualified individual with a disability, you may request a reasonable accommodation in Spectrum Health's application process. Contact us at 616-486-SHHR (7447).
Spectrum Health grants equal employment opportunity to all qualified persons without regard to race, color, national origin, sex, disability, age, religion, genetic information, marital status, height, weight, sexual orientation, veteran status, or any other legally protected
category. See more here.