RN Clinical Research Coordinator — Impactful Studies

Corewell Health; Reed City (MI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

On-demand pay Payactiv

Discounts directory

Identity protection (optional)

Retirement plan with match

Job summary

Corewell Health seeks a Clinical Research Coordinator to work under PI oversight in Reed City, MI, supporting a range of oncology-related studies. You will coordinate study activities, prepare IRB documents, recruit and enroll subjects, and ensure data quality across multiple systems.

The role requires a health/science degree, RN licensure, and BLS/ACLS/PALS training as applicable, with 1+ year of clinical research experience. On-site schedule is 40 hours weekly with day shifts.

Qualifications

• Required Bachelor's Degree or equivalent in a health or science related field.
• 1 year of relevant experience In clinical research and project management Preferred.
• Registered Nurse (RN) - State of Michigan Upon Hire required.
• Basic Life Support (BLS) - AHA American Heart Association 90 Days required Or
• Basic Life Support (BLS) - ARC American Red Cross 90 Days required.
• Shipping and Handling of Specimen Training-Certification - UNKNOWN Unknown 90 Days required.
• Adv Cardiovascular Life Support (ACLS) - AHA American Heart Association As Needed-required when indicated by the clinical trial protocol
• Pediatric Adv Life Support (PALS) - AHA American Heart Association As Needed-required when indicated by the clinical trial protocol

Responsibilities

• Serves 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, assesses eligibility, and enrolls subjects per protocol; with appropriate training and delegation, performs protocol-required research activities.
• Assesses patient status; collects, reviews, and documents data into a variety of systems per protocol.
• Assesses, plans, implements and evaluates educational programs, procedure and protocol updates to meet the identified needs of physician investigators, nursing staff, program staff, patients, family and/or the community.
• 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: respiratory therapy assessments; identification of adverse events; investigational product/test article (drug or device) accountability and administration; 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).

Skills

Project coordination

Clinical research coordination

Project management

RN (registered nurse)

Education

Bachelor's degree in health/science

Registered Nurse (RN) license

Job description

Corewell Health seeks a Clinical Research Coordinator to work under PI oversight in Reed City, MI, supporting a range of oncology-related studies. You will coordinate study activities, prepare IRB documents, recruit and enroll subjects, and ensure data quality across multiple systems.

The role requires a health/science degree, RN licensure, and BLS/ACLS/PALS training as applicable, with 1+ year of clinical research experience. On-site schedule is 40 hours weekly with day shifts.