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MI_SMHC Trinity Health - Michigan
Grand Rapids, MI | Full Time
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Clinical Research Coordinator
$63k-81k (estimate)
Full Time Just Posted
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MI_SMHC Trinity Health - Michigan is Hiring a Clinical Research Coordinator Near Grand Rapids, MI

Employment Type: Full time Shift: Day Shift Description: Position Summary: Coordinates and participates in clinical research studies conducted by principal investigator(s) at Trinity Health Grands Rapids & Trinity Health Muskegon, including a variety of complex activities involved in the collection, compilation and analysis of clinical research data, and oversees the screening for recruitment of research participants. Maintains 24-hour responsibility for the implementation and maintenance of clinical research studies including communication regarding protocol changes, completion of records, and IRB applications. What the Clinical Research Coordinator will need: Graduation from an accredited degree program in a clinical field such as Registered Nurse (RN) BSN or equivalent background and experience, plus two years of clinical trial research experience. Current valid Michigan licensure or certification in specialty field (Registered Nurse) as applicable. CPR certification or acquisition within 90 days of employment. Successful completion of department based research orientation program upon hire. Two (2) years prior clinical trial experience. Prior experience in clinical monitoring or as a study coordinator required. What the Clinical Research Coordinator will do: Coordinates and participates in clinical research studies conducted by principal investigators at Trinity Health Grands Rapids & Trinity Health Muskegon, including study start up, participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Assists in the determination of guidelines for the collection of clinical data and/or administration of clinical studies. Ensures compliance with study protocols, regulatory agency guidelines, and identification of inconsistencies and monitoring of patient progress including completion of documentation and reporting of adverse events. Prepares IRB applications, amendments to protocols, annual reports and serves as point person to IRB in absence of PI. Coordinates and implements procedures to support the collection of data from processes and procedures to collect data from source documents including (but not limited to) patient records, interviews, questionnaires and surveys, tests and other sources. Skilled in document coding, evaluation and interpretation of data. Preparation of study related regulatory documents as well as acquisition and preparation of study samples, cultures, tissues and other lab specimens for transport to study sponsors. Evaluates and interprets clinical data and preparation of presentations, papers, reports and analyses in conjunction with principal investigator(s). Collaborates on preparation of manuscripts for publication and opportunities for the development of investigator-initiated studies. Our Commitment to Diversity and Inclusion Trinity Health is one of the largest not-for-profit, Catholic healthcare systems in the nation. Built on the foundation of our Mission and Core Values, we integrate diversity, equity, and inclusion in all that we do. Our colleagues have different lived experiences, customs, abilities, and talents. Together, we become our best selves. A diverse and inclusive workforce provides the most accessible and equitable care for those we serve. Trinity Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by law. Trinity Health is one of the largest not-for-profit, faith-based health care systems in the nation. Together, we’re 121,000 colleagues and nearly 36,500 physicians and clinicians caring for diverse communities across 27 states. Nationally recognized for care and experience, our system includes 101 hospitals, 126 continuing care locations, the second largest PACE program in the country, 136 urgent care locations, and many other health and well-being services. Based in Livonia, Michigan, in fiscal year 2023, we invested $1.5 billion in our communities through charity care and other community benefit programs. For more information, visit http://www.trinity-health.org. You can also follow Trinity Health on LinkedIn.

Job Summary

JOB TYPE

Full Time

SALARY

$63k-81k (estimate)

POST DATE

06/02/2024

EXPIRATION DATE

08/01/2024

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The job skills required for Clinical Research Coordinator include Clinical Research, Clinical Trial, Presentation, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator. Select any job title you are interested in and start to search job requirements.

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The following is the career advancement route for Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator. You can explore the career advancement for a Clinical Research Coordinator below and select your interested title to get hiring information.

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