Clinical Research Specialist

Spectrum Health is a not-for-profit health system, based in West Michigan, offering a full continuum of care through the Spectrum Health Hospital Group, which is comprised of 12 hospitals, including Helen DeVos Children's Hospital; 180 ambulatory and service sites; 3,400 physicians and advanced practice providers, including 1,500 members of the Spectrum Health Medical Group; and Priority Health, a health plan with 788,000 members. Spectrum Health is West Michigan's largest employer, with 25,700 employees. The organization provided $372 million in community benefit during its 2017 fiscal year. Spectrum Health was named one of the nation's 15 Top Health Systems-and in the top five among the largest health systems-in 2017 by Truven Health Analytics®, part of IBM Watson HealthTM. This is the sixth time the organization has received this recognition. Our mission is to improve the health of the communities we serve. Our vision is for Spectrum Health will be the national leader for health by 2020. Our employees live our values of Excellence, Integrity, Compassion, Teamwork and Respect. For all of our latest job openings, news, and updates, please join our Talent Community:

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).

Supports research studies by coordinating, evaluating, and implementing clinical research activities under principal investigator oversight.

United States

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).Requirements:<ul><li> Bachelor's Degree in health or science related field or equivalent</li><li> CRT-Basic Life Support (BLS) - ARC American Red Cross 90 Days or CRT-Basic Life Support (BLS) - AHA American Heart Association 90 Days</li><li> 1 year of relevant experience in clinical research and project management</li></ul>Benefits:<ul><li> Comprehensive benefits package to meet your financial, health, and work/life balance goals</li><li> On-demand pay program powered by Payactiv</li><li> Discounts directory with deals on restaurants, phone plans, spas, and more</li><li> Optional identity theft protection, home and auto insurance, pet insurance</li><li> Traditional and Roth retirement options with service contribution and match savings</li></ul>

Corewell Health

Clinical Research Specialist Supports research studies by coordinating, evaluating, and implementing clinical research activities under principal investigator oversight. 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). Clinical Research Specialist Research Scientist Corewell Health hospitals-and-health-care healthcare-services medical-practices emergency-and-relief-services research-services anesthesiology association cardiovascular diagnostic-services doctors emergency-medicine emergency-rooms ent family-practice general gyn gynecology health health-care healthcare hematology hospital hospital-and-health-care hospitals internal-medicine laboratory-testing medical neurology non-profit non-profit-services non-profits ob obstetrics oncology ophthalmologists ophthalmology orthopaedic-surgery orthopedics pathology pediatrics physical-therapy psychiatry radiology urgent-care urology vascular-surgery Grand Rapids

The role involves managing research studies, recruiting subjects, collecting data, and ensuring compliance with regulations. It requires collaboration with various stakeholders to advance clinical practice through research.

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