Clinical Research Specialist 1

Corewell Health

Grand Rapids, MIOn-siteFull time
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Location
Grand Rapids, MI
Work style
On-site
Job type
Full time
Posted
Oct 26
1 day ago
Career path

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About the company

Corewell Health

Hospital & health care · 10,001+ employees

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.

Corewell Health on LinkedIn

What you'll do

  • Serve as primary coordinator / project manager on research studies
  • Evaluate and prepare research studies for implementation
  • Identify, recruit, screen, and enroll eligible subjects
  • Perform protocol-required research activities and procedures
  • Monitor patient status and collect, review, and document data
  • Maintain research studies in compliance with laws, GCP, contracts, and policies
  • Coordinate or perform study activities, including adverse event identification
  • Communicate and collaborate with sponsors, research centers, and the multidisciplinary team

What you need

  • Bachelor's Degree in health or science related field or equivalent
  • CRT-Basic Life Support (BLS) - ARC American Red Cross within 90 days or
  • CRT-Basic Life Support (BLS) - AHA American Heart Association within 90 days
  • 1 year of relevant experience in clinical research and project management (preferred)

Key skills

clinical researchproject managementIRB documentsGCPBasic Life Support (BLS)

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Perks

  • Comprehensive benefits package
  • On-demand pay program
  • Discounts directory
  • identity theft protection
  • home and auto insurance
  • Traditional and Roth retirement options
  • service contribution and match savings

See full description on company page, apply now

Read the full posting here
Hybrid schedule requires 2-3 days onsite in Grand Rapids Job Summary With principal investigator oversight, prepares, evaluates and implements research studies to enhance the advancement of clinical practice. 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 How Corewell Health cares for you Comprehensive benefits package to meet your financial, health, and work/life balance goals. Learn more here . On-demand 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 Traditional and Roth retirement options with service contribution and match savings Eligibility for benefits is determined by employment type and status Primary Location SITE - Secchia Center - 15 Michigan St NE - Grand Rapids Department Name Sponsored Programs Heart and Vascular Institute Research Operations - Grand Rapids Hosp Employment Type Full time Shift Day (United States of America) Weekly Scheduled Hours 40 Hours of Work 8:00a - 4:30p Days Worked Monday - Friday Weekend Frequency Variable weekends CURRENT COREWELL HEALTH TEAM MEMBERS – Please apply through Find Jobs from your Workday team member account. This career site is for Non-Corewell Health team members only. Corewell Health is committed to providing a safe environment for our team members, patients, visitors, and community. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site 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.

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