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Clinical Research Coordinator 3 – Orthopedic Surgery

Rush University Medical Center

This is a Contract position in Chicago, IL posted July 28, 2019.

Job Title: Clinical Research Coordinator 3
– Orthopedic Surgery Department: Shift: 1st Specialty: Orthopedic Surgery Job Number: 2019-1804 Date Posted: 06/10/2019 Position Type: Research Job Qualifications: At Rush University Medical Center, we are committed to advancing scientific medical knowledge through research.

We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability.

Are you looking to be a part of the exciting, always evolving and expanding new developments in research here at Rush University Medical Center?

Are you well experienced in working with a variety of group, single and industry oriented studies?

If this describes you, you may be the right candidate for the Clinical Research Coordinator 3 position with the Department of Orthopedic Surgery Research.

Position Summary: The Clinical Research Coordinator III, under the Clinical Research Manager, leads more complex clinical research studies conducted by PI(s) which may include grant-funded, industry sponsored, and investigator-initiated clinical research studies.

S/he will partner with the PI to manage multiple complex clinical research studies and supervises a team of 5 or more Clinical Research Staff.

The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.

Position Responsibilities: Supervises coordination of all aspects of the study including recruitment, consent, screening, scheduling, and tracking and provides study updates to study participants throughout the conduct of the study.

Ensures data is entered into the study¡¦s electronic data capture system and queries are responded to and resolved in a timely manner.

Oversees the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.

May supervise the collection, processing and shipment of potentially biohazardous specimens May supervise administration of structured tests and questionnaires according to research study protocols including the utilization of study-related technology and equipment as part of assessment procedures.

Reviews and finalizes summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance and ensures accurate study updates are provided throughout the conduct of the study Lead the development of any required action plans in conjunction with researcher Ensure unanticipated problems (protocol deviations, adverse events, and serious adverse events) are submitted in a timely manner Provide recommendations to proactively address complex issues and/or variances with study related activities Train and mentor clinical research staff members within the department.

Conduct performance reviews and annual evaluations of staff May summarize and share relevant research during internal and external presentations.

Maintains current knowledge of industry trends Required Job Qualifications: Bachelor’s degree required; with science or health related field preferred 5-7 years of clinical research experience required; with a minimum of 5 years coordinating Human Subjects research Demonstrated advanced knowledge of Good Clinical Practices and Good Documentation Practices Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research Relevant certification required as a Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP) Strong project management skills Demonstrated problem-solving, critical decision makings and professional judgement Strong analytical and organizational skills with a high attention to details Demonstrated ability to build rapport , navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants and vendors Strong verbal and written communication with ability to communicate complex concepts to multiple audiences Demonstrated ability to collaborate within multi-disciplinary team settings Travel may be required Preferred Job Qualifications: Master’s degree with science or health related field preferred Prior supervisory experience Spine experience preferred Company Highlights: Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career.

Everything we do centers on one goal: improving patient care.

The Association for the Accreditation of Human Research Protection Programs (AAHRPP) has awarded Rush full accreditation for three years.

Rush is one of the first academic medical centers in Illinois to receive this accreditation.

As an academic medical center, Rush University Medical Center in Chicago, Illinois, is committed to advancing medical knowledge through research.

Investigators at Rush are involved in more than 1,600 projects, including hundreds of clinical studies to test the effectiveness and safety of new therapies and medical devices, as well as to expand scientific and medical knowledge.

RUMC offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements.

Rush University is home to one of the first medical colleges in the Midwest and one of the nation’s top-ranked nursing colleges, as well as graduate programs in allied health, health systems management and biomedical research.

Rush University Medical Center is an Equal Opportunity Employer that welcomes and encourages all applicants to apply regardless of age, race, sex, religion, color, national origin, disability, veteran status, sexual orientation, gender identity and/or expression, marital or parental status, ancestry, citizenship status, pregnancy or other reason prohibited by law.

At Rush University Medical Center, we are committed to advancing scientific medical knowledge through research.

We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability.

Are you looking to be a part of the exciting, always evolving and expanding new developments in research here at Rush University Medical Center?

Are you well experienced in working with a variety of group, single and industry oriented studies?

If this describes you, you may be the right candidate for the Clinical Research Coordinator 3 position with the Department of Orthopedic Surgery Research.

Position Summary: The Clinical Research Coordinator III, under the Clinical Research Manager, leads more complex clinical research studies conducted by PI(s) which may include grant-funded, industry sponsored, and investigator-initiated clinical research studies.

S/he will partner with the PI to manage multiple complex clinical research studies and supervises a team of 5 or more Clinical Research Staff.

The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.

Position Responsibilities: Supervises coordination of all aspects of the study including recruitment, consent, screening, scheduling, and tracking and provides study updates to study participants throughout the conduct of the study.

Ensures data is entered into the study¡¦s electronic data capture system and queries are responded to and resolved in a timely manner.

Oversees the submission of study related documents, study protocols and study protocol amendments to the IRB per policy and procedure Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.

May supervise the collection, processing and shipment of potentially biohazardous specimens May supervise administration of structured tests and questionnaires according to research study protocols including the utilization of study-related technology and equipment as part of assessment procedures.

Reviews and finalizes summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance and ensures accurate study updates are provided throughout the conduct of the study Lead the development of any required action plans in conjunction with researcher Ensure unanticipated problems (protocol deviations, adverse events, and serious adverse events) are submitted in a timely manner Provide recommendations to proactively address complex issues and/or variances with study related activities Train and mentor clinical research staff members within the department.

Conduct performance reviews and annual evaluations of staff May summarize and share relevant research during internal and external presentations.

Maintains current knowledge of industry trends Required Job Qualifications: Bachelor’s degree required; with science or health related field preferred 5-7 years of clinical research experience required; with a minimum of 5 years coordinating Human Subjects research Demonstrated advanced knowledge of Good Clinical Practices and Good Documentation Practices Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research Relevant certification required as a Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP) Strong project management skills Demonstrated problem-solving, critical decision makings and professional judgement Strong analytical and organizational skills with a high attention to details Demonstrated ability to build rapport , navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants and vendors Strong verbal and written communication with ability to communicate complex concepts to multiple audiences Demonstrated ability to collaborate within multi-disciplinary team settings Travel may be required Preferred Job Qualifications: Master’s degree with science or health related field preferred Prior supervisory experience Spine experience preferred Company Highlights: Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career.

Everything we do centers on one goal: improving patient care.

The Association for the Accreditation of Human Research Protection Programs (AAHRPP) has awarded Rush full accreditation for three years.

Rush is one of the first academic medical centers in Illinois to receive this accreditation.

As an academic medical center, Rush University Medical Center in Chicago, Illinois, is committed to advancing medical knowledge through research.

Investigators at Rush are involved in more than 1,600 projects, including hundreds of clinical studies to test the effectiveness and safety of new therapies and medical devices, as well as to expand scientific and medical knowledge.

RUMC offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements.

Rush University is home to one of the first medical colleges in the Midwest and one of the nation’s top-ranked nursing colleges, as well as graduate programs in allied health, health systems management and biomedical research.

Rush University Medical Center is an Equal Opportunity Employer that welcomes and encourages all applicants to apply regardless of age, race, sex, religion, color, national origin, disability, veteran status, sexual orientation, gender identity and/or expression, marital or parental status, ancestry, citizenship status, pregnancy or other reason prohibited by law.