Qureos Mentor

Innovo Research

<div>JOB SUMMARY
The Senior CRC will work closely with Principal Investigators and clinical research teams to coordinate the daily operations of clinical research studies and oversee clinical research staff performing clinical functions at the designated Innovo Research partner site The Senior CRC will be responsible for making sure that all clinical research activities are efficiently executed, and conducted in a professional manner that is compliant with all human research subject regulations.
RESPONSIBILITIES<ul><li>
Assist with mentoring and training clinical research staff.</li><li>
Perform clinical functions i.e. phlebotomy, monitoring vital signs on study participants, etc., when warranted; educate family and contribute to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.</li><li>
Liaises with agencies, pharmaceutical companies, laboratories, vendors, equipment, and supply companies as needed; oversees availability of supplies and/or equipment for studies.</li><li>
Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow&mdash;up, collect patient/ research participant history, collect and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.</li><li>
Develop strong working relationships and maintain effective communication with study team members.</li><li>
Completes all protocol-related training and adheres to IRB approved protocol(s)</li><li>
Support the collection and review of required essential study documents and reports.
</li><li>Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.).</li><li>
Assist in the informed consent process of research subjects.</li><li>
Support and advocate for the safety of research subjects.</li><li>
Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close-out activities.</li><li>
Collect, process, and ship laboratory specimens.</li><li>
Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.</li><li>
Performs all additional duties as assigned.</li></ul><div>
Qualifications<ul><li>
At least 3-5 years of experience coordinating clinical trials, including the activities listed above.
</li><li>BS/BA in Life Science or related discipline.
</li><li>Certified Clinical Research Coordinator (CCRC) certification preferred.</li><li>
Previous GCP training and certification required and working knowledge of current ICH GCP guidelines and applicable regulations. Experience in a clinical setting.</li><li>
Demonstrated ability in positive relationship building.
</li><li>Previous experience with training and mentoring other clinical research professionals is a plus.</li><li>
Strong interpersonal skills with attention to detail a must. Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities.</li><li>
Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
</li><li>Strong organization/prioritization skills for the management of multiple concurrent projects.
</li><li>An understanding of Regulatory and Central/Local ethic submission processes
</li><li>Ability to manage multiple competing priorities within various clinical trials.
</li><li>Excellent verbal and written communication skills required.
</li><li>Ability to work independently, prioritize, and work with a matrix team environment is essential.
</li><li>Ability to travel for Clinic activities, and attend investigator meetings or vendor visits/audits, as required.
</li></ul>BENEFITS (full-time)
</div><div><ul><li>Competitive salary</li><li>
Health Insurance</li><li>
Dental Insurance</li><li>
Disability Insurance</li><li>
Life Insurance</li><li>
Paid Time Off</li><li>
Vision Insurance</li></ul>
</div>WORKING CONDITIONS
This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.</div>

Senior Clinical Research Coordinator

<div>
 
 Description
 
 
 
 
 JOB SUMMARY
 
 
 
 A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
 </li>
 <ul>
 <li>
 Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.
 </li>
 <li>
 Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
 </li>
 <li>
 Recruit and screen participants for clinical trials and maintain subject screening logs.
 </li>
 <li>
 Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.
 </li>
 <li>
 Maintain source documentation based on protocol requirements.
 </li>
 <li>
 Schedule and execute study visits and perform study procedures.
 </li>
 <li>
 Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
 </li>
 <li>
 Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.
 </li>
 <li>
 Correspond with research subjects and troubleshoot study-related questions or issues.
 </li>
 <li>
 Participate in ?huddles? to confirm daily study tasks are assigned to team members and are executed to the expected standards.
 </li>
 </ul>
 <li>
 Assist with study data quality checking and query resolution.
 </li>
 <li>
 Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
 </li>
 <li>
 Assist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.
 </li>
 <li>
 Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
 </li>
 <li>
 Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
 </li>
 <li>
 Assist the research site with coverage planning related to staffing and scheduling for research studies.
 </li>
 <li>
 Monitor subject safety and report adverse reactions to appropriate medical personnel.
 </li>
 <li>
 Maintain confidentiality of data and PHI as required.
 </li>
 <li>
 Collaborate with provider offices to carry out research in the most efficient workflow possible.
 </li>
 <li>
 Maintains stock of supplies needed to carry out each study per protocol.
 </li>
 <li>
 Performs other duties and projects as assigned.
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 QUALIFICATIONS
 
 
 
 <ul>
 <li>
 Bachelor's degree in a related field
 </li>
 <li>
 1-2 years of clinical research experience
 </li>
 <li>
 Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience
 </li>
 <li>
 Proficient in the use of Microsoft Office applications
 </li>
 <li>
 Understanding of medical terminology
 </li>
 <li>
 Working knowledge of clinical trials
 </li>
 <li>
 Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.
 </li>
 <li>
 In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
 </li>
 <li>
 Skilled in carrying out required clinical procedures such as phlebotomy and vital signs.
 </li>
 <li>
 Strong written and verbal communication skills including good command of the English language.
 </li>
 <li>
 Skill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.
 </li>
 <li>
 Skill in preparing/maintaining records, writing reports, and responding to correspondence.
 </li>
 <li>
 Ability to maintain quality control standards.
 </li>
 <li>
 Ability to react calmly and effectively in all situations.
 </li>
 <li>
 Excellent organizational and problem-solving skills.
 </li>
 <li>
 Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.
 </li>
 <li>
 Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
 </li>
 <li>
 Practice a high level of integrity, honesty, and in maintaining confidentiality.
 
 
 </li>
 </ul>
 
 BENEFITS (Full-Time)
 
 
 
 <ul>
 <li>
 Competitive salary
 </li>
 <li>
 Health Insurance
 </li>
 <li>
 Dental Insurance
 </li>
 <li>
 Disability Insurance
 </li>
 <li>
 Life Insurance
 </li>
 <li>
 Paid Time Off
 </li>
 <li>
 Vision Insurance
 
 
 </li>
 </ul>
 
 WORKING CONDITIONS
 
 
 
 This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
 
 
 Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
 
 
 The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
 
 
 Applicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.
</div>

Clinical Research Coordinator

<div>PLEASE NOTE: The location and site listed for this job are incorrect. This position will be located in Dubuque, Iowa.
JOB SUMMARY
A Clinical Research Nurse is a member of the research team who serves participants in clinical trials with direct patient care. This position is responsible for maintaining tight regulatory control over the health and safety of patients, as well as gathering and analyzing data for scientific study.
RESPONSIBILITIES<ul><li>
Perform clinical functions i.e. phlebotomy, monitoring vital signs of study participants, etc., when warranted; educate family and contribute to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.</li><li>
Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow&mdash;up, collect patient/ research participant history, collect, and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.</li><li>
Under the supervision of an investigator, conduct health assessments as medically necessary or required per protocol to assess or resolve adverse events, safety, and general health of study participants.</li><li>
Monitor study participants for adverse events and report any adverse events to the principal investigator, and study coordinator, if applicable.</li><li>
Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license.</li><li>
Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials.</li><li>
Perform and adhere to clinical functions commensurate with pertinent nursing license scope of practice (i.e., keep within state Board of Nursing scope of practice for license as an LPN, RN, etc.)
</li><li>Maintain compliance with required hospital and unit-specific training competencies as well as an active nursing license status with the state Board of Nursing</li><li>
Perform diagnostic tests and monitor participants&rsquo; health through regular assessments.</li><li>
Observe, document, and report any changes in participant&rsquo;s health status, and provide clinical care where necessary.</li><li>
Respond to emergencies and provide medical care as necessary and/or directed by a study investigator.</li><li>
Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks.</li><li>
Assist in the informed consent process of research subjects, if appropriate for scope of license.</li><li>
Support and advocate for the safety of research subjects.</li><li>
Collect, process, and ship laboratory specimens.</li><li>
Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.</li><li>
Provide training to new investigator/site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.</li><li>
Performs all additional duties as assigned.</li></ul><div>
Qualifications<ul><li>
Current RN/LPN licensure in the state of employment.
</li><li>Associate Degree in Nursing from an accredited school of nursing.
</li><li>Certification in Clinical Research Coordination (CCRC) preferred.</li><li>
BLS required</li><li>
Three years prior experience in a health-related clinic or research setting</li><li>
Proficient in the use of Microsoft Office applications</li><li>
Understanding of medical terminology</li><li>
Strong organizational skills</li><li>
Working knowledge of clinical trials
</li><li>Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.</li><li>
Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
</li><li>Practice a high level of integrity, honesty, and in maintaining confidentiality.</li></ul>
Benefits (full-time)</div><div><ul><li>
Competitive Salary</li><li>
Health Insurance</li><li>
Dental Insurance
</li><li>Disability Insurance</li><li>
Life Insurance</li><li>
Paid Time Off</li><li>
Vision Insurance</li></ul></div>
WORKING CONDITIONS
This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.</div>

Clinical Research Nurse

<div>JOB SUMMARY
A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.
RESPONSIBILITIES<ul><li>
Provide clinical research support to investigators to prepare for and execute assigned research studies, including:<ul><li>
Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.</li><li>
Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.</li><li>
Recruit and screen participants for clinical trials and maintain subject screening logs.</li><li>
Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.</li><li>
Maintain source documentation based on protocol requirements.</li><li>
Schedule and execute study visits and perform study procedures.</li><li>
Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.</li><li>
Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.</li><li>
Correspond with research subjects and troubleshoot study-related questions or issues.</li><li>
Participate in &ldquo;huddles&rdquo; to confirm daily study tasks are assigned to team members and are executed to the expected standards.</li></ul></li><li>
Assist with study data quality checking and query resolution.</li><li>
Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
</li><li>Assist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.</li><li>
Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.</li><li>
Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.</li><li>
Assist the research site with coverage planning related to staffing and scheduling for research studies.</li><li>
Monitor subject safety and report adverse reactions to appropriate medical personnel.</li><li>
Maintain confidentiality of data and PHI as required.</li><li>
Collaborate with provider offices to carry out research in the most efficient workflow possible.</li><li>
Maintains stock of supplies needed to carry out each study per protocol.</li><li>
Performs other duties and projects as assigned.</li></ul>
QUALIFICATIONS<ul><li>
Bachelor's degree in a related field</li><li>
1-2 years of clinical research experience</li><li>
Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience
</li><li>Proficient in the use of Microsoft Office applications</li><li>
Understanding of medical terminology</li><li>
Working knowledge of clinical trials
</li><li>Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.</li><li>
In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
</li><li>Skilled in carrying out required clinical procedures such as phlebotomy and vital signs.</li><li>
Strong written and verbal communication skills including good command of the English language.</li><li>
Skill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care.
</li><li>Skill in preparing/maintaining records, writing reports, and responding to correspondence.
</li><li>Ability to maintain quality control standards.
</li><li>Ability to react calmly and effectively in all situations.
</li><li>Excellent organizational and problem-solving skills.</li><li>
Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.</li><li>
Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
</li><li>Practice a high level of integrity, honesty, and in maintaining confidentiality.</li></ul>
<div>BENEFITS (Full-Time)<ul><li>
Competitive salary</li><li>
Health Insurance</li><li>
Dental Insurance</li><li>
Disability Insurance</li><li>
Life Insurance</li><li>
Paid Time Off</li><li>
Vision Insurance</li></ul></div>
WORKING CONDITIONS
This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
Applicants must be authorized to work for ANY employer in the U.S. Innovo Research is unable to sponsor or take over sponsorship of an employment Visa at this time.</div>

Join Innovo Research and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Innovo Research

About Company

Senior Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Nurse

Clinical Research Coordinator