RN Clinical Research
RN Clinical Research
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Scope of Work
With principal investigator oversight prepares evaluates and implements research studies to enhance the advancement of clinical practice; effectively manages all aspects of research studies.
Essential Functions
Serves as primary coordinator / project manager on a variety of research studies of greater regulatory clinical and operational complexity (e.g. investigatorinitiated Phase IIII clinical trials locallyheld IND/IDE coordinating center of multisite studies federallyfunded research etc..
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); assists in data/statistical analysis manuscript preparation and results dissemination; assists with grant development and reporting; attends study meetings.
Identifies recruits screens assesses eligibility and enrolls subjects per protocol; with appropriate training and delegation performs protocolrequired research activities.
With appropriate training and delegation assesses patient status; collects reviews and documents data into a variety of systems per protocol; generates and manages databases.
Acts as mentor to new research staff on research process and regulations; 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).
Participates and/or leads regular research quality management activities to ensure research studies are in compliance with federal state and local law GCP contracts and institutional policies.
Coordinates and/or performs study activities which may include: nursing 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; may act as project manager for animal studies (including protocol development and IACUC applications).
Actively promotes research activities within the organization and community; may give external presentations write journal articles and/or be a cited author on publications; 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.
Qualifications
Required Bachelors Degree in a health or science related field
Preferred Masters Degree
3 years of relevant experience CRN I or equivalent clinical research experience Required
Relevant research quality management experience Required
LICRegistered Nurse (RN) STATEMI State of Michigan Upon Hire required
CRTBasic Life Support (BLS) AHA American Heart Association 90 Days required Or
CRTBasic Life Support (BLS) ARC American Red Cross 90 Days required
CRTClinical Research Coordinator Certified (CCRC) ACRP Association of Clinical Research Professionals Upon Hire required
CRTShipping and Handling of Specimen TrainingCertification UNKNOWN Unknown 90 Days required
CRTAdv Cardiovascular Life Support (ACLS) AHA American Heart Association As neededrequired when indicated by the clinical trial protocol
CRTPediatric Adv Life Support (PALS) AHA American Heart Association As neededrequired when indicated by the clinical trial protocol
How Corewell Health cares for you
Comprehensive benefits package to meet your financial health and work/life balance goals. Learn more here.
Ondemand pay program powered by Payactiv
Discounts directory with deals on the things that matter to you like restaurants phone plans spas and more!
Optional identity theft protection home and auto insurance pet insurance
Traditional and Roth retirement options with service contribution and match savings
Eligibility for benefits is determined by employment type and status
Primary Location
SITE LemmenHolton Cancer Pavilion 145 Michigan St Grand RapidsDepartment Name
Pulmonary and Acute Health Research Operations GREmployment Type
Full timeShift
Day (United States of America)Weekly Scheduled Hours
40Hours of Work
8:00 a.m. to 4:30 p.m.Days Worked
Monday to FridayWeekend Frequency
Variable weekendsCURRENT COREWELL HEALTH TEAM MEMBERS Please apply through Find Jobs from your Workday team member account. This career site is for NonCorewell Health team members only.
Corewell Health is committed to providing a safe environment for our team members patients visitors and community. We require a drugfree workplace and require team members to comply with the MMR Varicella Tdap and Influenza vaccine requirement if in an onsite or hybrid workplace category. We are committed to supporting prospective team members who require reasonable accommodations to participate in the job application process to perform the essential functions of a job or to enjoy equal benefits and privileges of employment due to a disability pregnancy or sincerely held religious belief.
Corewell 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 gender pregnancy sexual orientation gender identity or expression veteran status or any other legally protected category.
An interconnected collaborative culture where all are encouraged to bring their whole selves to work is vital to the health of our organization. As a health system we advocate for equity as we care for our patients our communities and each other. From workshops that develop cultural intelligence to our inclusion resource groups for people to find community and empowerment at work we are dedicated to ongoing resources that advance our values of diversity equity and inclusion in all that we do. We invite those that share in our commitment to join our team.
You may request assistance in completing the application process by calling 616.486.7447.
Employment Type
Full-Time
