Clinical Research Coordinator II - Pulmonary Medicine (Grossoehme)
DEPARTMENT: Pulmonary Medicine, Cincinnati Children's Research Foundation, CCHMC Affiliates
PRIMARY FOCI INCLUDE: Psychosocial factors related to improved health outcomesamong persons followed by cystic fibrosis, transgender or palliative care teams,as well as improving outcomes in hospital safety and physician behavior.
SCOPE OF WORK: This position includes direct patient/family contactfor recruiting, informed consent and may include conducting semi-structuredinterviews and or intervention delivery, as well as participation inqualitative research analysis of interviews and documents, and maintainingregulatory documentation. Data entry may be required periodically. Supervision of students may be included from time to time. This positionrequires travel to CCHMC satellite or other locations and may include out oftown travel periodically. Experience in a clinical research setting is preferred.
SUPERVISOR'S TITLE: Principal Investigator, Business Director, Clinical Director, Business Manager, Clinical Research Manager
TITLES SUPERVISED: N/A
TOTAL NUMBER OF FTEs DIRECTLY OR INDIRECTLY SUPERVISED: 0
PURPOSE OF POSITION: To assist in planning and conducting clinical research for an assigned division of a Medical Center dedicated to the care of infants, children and adolescents. To perform clinical research according to established procedures, to make accurate observations, record test results and to make recommendations for new methods based upon outcome.
Responsibilities
Study Conduct/ Clinical Research Practice
Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor. Assemble lab kits and/or gather supplies. Collect and label samples as instructed and deliver or process samples in accordance with the protocol, manual of operations, standard operating procedure (SOP) or other work instruction set. Ensure specimens are properly logged, handled and stored. Follow direction of clinical research coordinator or others involved in the clinical research project work. Assist other staff members and coordinators to implement studies. Maintain inventory of supplies and equipment. Operate standard laboratory and research study equipment, if applicable. Troubleshoot and correct erroneous results or problems with equipment.
Regulatory Compliance and Documentation
Demonstrate accuracy and organizational skills and the ability to follow through on requests and meet timelines. Identify regulatory activities to be completed and takes the initiative to complete. Coordinate and participate in the assembly of materials. Assist in maintaining up-to-date and accurate written and electronic records and files to support clinical research activities. Assist with audit readiness records review and preparation activities. Assist with maintaining protocol specific SOP's, IRB and regulatory correspondence. Demonstrate an awareness of federal regulations; state and local law; GCP/ICH and CCHMC policies to promote ethical practices in research involving human participants and to ensure compliance to those regulations. Recognize the importance of reporting concerns of ethical and/or regulatory issues to supervisor in a timely manner. Assist with the documentation of regulatory activities and maintenance of the regulatory binder in keeping with the institution and division SOPs. Complete required training. Seek out research educational opportunities.
Recruitment/Enrollment/Retention
Maintain awareness of status of all active studies. Identify potentially eligible participants. Coordinate, plan and execute study visits and provide instructions and reimbursement to participants. Approach potential participants and families in a professional manner. Conduct pre-consent screening procedures according to protocol specifications to determine eligibility. Review consent form with participant and provide time for participant to consider study participation. Execute the informed consent process according to Good Clinical Practices (GCP), CCHMC procedures and other applicable policies. Communicate with participants' clinical team regarding study participation as indicated by protocol and/or manual of operations. Document in applicable systems (tracking, electronic health, etc.) participants approached, screened and enrolled in the study. Communicate challenges with recruitment and retention to the study leadership. Provide recommendations to improve recruitment and retention to the study leadership.
Communication
Assist with organizing and filing all correspondence. Refer questions and issues that arise during study conduct to the appropriate research team member. Maintain awareness of study related issues involving investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions. Maintain relationship with participants. Develop a rapport with study participants. Provide input to division discussions related to clinical research studies. Participate in meetings, discussions and activities designed to improve organizational performance through recommending areas or approaches for improving study conduct.
Data Management
Complete Case Report Forms (CRFs) and source documentation in compliance with all applicable guidelines for human research. Review CRFs to ensure completeness, accuracy and compliance with Good Clinical Practice. Enter data into various auditable databases or electronic data-capture systems. Maintain internal record keeping system(s) in conjunction with study team members. Ensure accuracy of documentation from sources. Perform quality checks to ensure accuracy of data. Review reports, tables, and listings. Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors.
Education
Coordinate training activities and assembles training materials in preparation and conduct of clinical trials. Assist in developing and delivering guidelines and educational materials for investigators, research support staff and the clinical team (as applicable). Complete required training. Participate in educational opportunities.
Skills & Competencies
Clerical Abilities
Ability to perform clerical functions with accuracy and attention to detail
Diversity Appreciation
Understanding and showing respect and appreciation for the uniqueness of all individuals; leveraging differences in others' perspectives and ideas; appreciating cultural differences and adjusting one's approach to successfully integrate with others who are different from oneself
Follow Instructions - Adv
Ability to follow complex written and verbal instructions
Scientific Terminology
Knowledge of scientific terminology
Computer Proficiency - Basic
Working knowledge of basic computer applications
Independence
Pursuing work with little supervision or assistance; directing one's own efforts. Demonstrated ability to work independently and as part of a team.
Organization
Strong organizational and project management skills to handle projects independently.
Communication - Advanced
Excellent verbal, written and interpersonal communication skills.
Equipment
Ability to operate laboratory equipment (if applicable to position)
Required:
Bachelor's degree OR
Associates Degree in a related field AND 2 years related experience OR
High School Graduate OR Equivalent AND 4 years related experience
Preferred:
Bachelor's Degree in a related field
Undergraduate research experience
1. -Excellentorganizational skills
2. -Ability to managemultiple tasks
3. -Ability tointeract with diverse populations, including minority populations, in ways thatset people at ease
4. -Attention todetail
5. -Excellentcommunication skills, both written and spoken
6. -Ability tofunction independently
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
PRIMARY FOCI INCLUDE: Psychosocial factors related to improved health outcomesamong persons followed by cystic fibrosis, transgender or palliative care teams,as well as improving outcomes in hospital safety and physician behavior.
SCOPE OF WORK: This position includes direct patient/family contactfor recruiting, informed consent and may include conducting semi-structuredinterviews and or intervention delivery, as well as participation inqualitative research analysis of interviews and documents, and maintainingregulatory documentation. Data entry may be required periodically. Supervision of students may be included from time to time. This positionrequires travel to CCHMC satellite or other locations and may include out oftown travel periodically. Experience in a clinical research setting is preferred.
SUPERVISOR'S TITLE: Principal Investigator, Business Director, Clinical Director, Business Manager, Clinical Research Manager
TITLES SUPERVISED: N/A
TOTAL NUMBER OF FTEs DIRECTLY OR INDIRECTLY SUPERVISED: 0
PURPOSE OF POSITION: To assist in planning and conducting clinical research for an assigned division of a Medical Center dedicated to the care of infants, children and adolescents. To perform clinical research according to established procedures, to make accurate observations, record test results and to make recommendations for new methods based upon outcome.
Responsibilities
Study Conduct/ Clinical Research Practice
Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor. Assemble lab kits and/or gather supplies. Collect and label samples as instructed and deliver or process samples in accordance with the protocol, manual of operations, standard operating procedure (SOP) or other work instruction set. Ensure specimens are properly logged, handled and stored. Follow direction of clinical research coordinator or others involved in the clinical research project work. Assist other staff members and coordinators to implement studies. Maintain inventory of supplies and equipment. Operate standard laboratory and research study equipment, if applicable. Troubleshoot and correct erroneous results or problems with equipment.
Regulatory Compliance and Documentation
Demonstrate accuracy and organizational skills and the ability to follow through on requests and meet timelines. Identify regulatory activities to be completed and takes the initiative to complete. Coordinate and participate in the assembly of materials. Assist in maintaining up-to-date and accurate written and electronic records and files to support clinical research activities. Assist with audit readiness records review and preparation activities. Assist with maintaining protocol specific SOP's, IRB and regulatory correspondence. Demonstrate an awareness of federal regulations; state and local law; GCP/ICH and CCHMC policies to promote ethical practices in research involving human participants and to ensure compliance to those regulations. Recognize the importance of reporting concerns of ethical and/or regulatory issues to supervisor in a timely manner. Assist with the documentation of regulatory activities and maintenance of the regulatory binder in keeping with the institution and division SOPs. Complete required training. Seek out research educational opportunities.
Recruitment/Enrollment/Retention
Maintain awareness of status of all active studies. Identify potentially eligible participants. Coordinate, plan and execute study visits and provide instructions and reimbursement to participants. Approach potential participants and families in a professional manner. Conduct pre-consent screening procedures according to protocol specifications to determine eligibility. Review consent form with participant and provide time for participant to consider study participation. Execute the informed consent process according to Good Clinical Practices (GCP), CCHMC procedures and other applicable policies. Communicate with participants' clinical team regarding study participation as indicated by protocol and/or manual of operations. Document in applicable systems (tracking, electronic health, etc.) participants approached, screened and enrolled in the study. Communicate challenges with recruitment and retention to the study leadership. Provide recommendations to improve recruitment and retention to the study leadership.
Communication
Assist with organizing and filing all correspondence. Refer questions and issues that arise during study conduct to the appropriate research team member. Maintain awareness of study related issues involving investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions. Maintain relationship with participants. Develop a rapport with study participants. Provide input to division discussions related to clinical research studies. Participate in meetings, discussions and activities designed to improve organizational performance through recommending areas or approaches for improving study conduct.
Data Management
Complete Case Report Forms (CRFs) and source documentation in compliance with all applicable guidelines for human research. Review CRFs to ensure completeness, accuracy and compliance with Good Clinical Practice. Enter data into various auditable databases or electronic data-capture systems. Maintain internal record keeping system(s) in conjunction with study team members. Ensure accuracy of documentation from sources. Perform quality checks to ensure accuracy of data. Review reports, tables, and listings. Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors.
Education
Coordinate training activities and assembles training materials in preparation and conduct of clinical trials. Assist in developing and delivering guidelines and educational materials for investigators, research support staff and the clinical team (as applicable). Complete required training. Participate in educational opportunities.
Skills & Competencies
Clerical Abilities
Ability to perform clerical functions with accuracy and attention to detail
Diversity Appreciation
Understanding and showing respect and appreciation for the uniqueness of all individuals; leveraging differences in others' perspectives and ideas; appreciating cultural differences and adjusting one's approach to successfully integrate with others who are different from oneself
Follow Instructions - Adv
Ability to follow complex written and verbal instructions
Scientific Terminology
Knowledge of scientific terminology
Computer Proficiency - Basic
Working knowledge of basic computer applications
Independence
Pursuing work with little supervision or assistance; directing one's own efforts. Demonstrated ability to work independently and as part of a team.
Organization
Strong organizational and project management skills to handle projects independently.
Communication - Advanced
Excellent verbal, written and interpersonal communication skills.
Equipment
Ability to operate laboratory equipment (if applicable to position)
Required:
Bachelor's degree OR
Associates Degree in a related field AND 2 years related experience OR
High School Graduate OR Equivalent AND 4 years related experience
Preferred:
Bachelor's Degree in a related field
Undergraduate research experience
1. -Excellentorganizational skills
2. -Ability to managemultiple tasks
3. -Ability tointeract with diverse populations, including minority populations, in ways thatset people at ease
4. -Attention todetail
5. -Excellentcommunication skills, both written and spoken
6. -Ability tofunction independently
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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